GSM3503183: D31_130_T1_20180323; Neisseria gonorrhoeae; ssRNA-seq

SRX5100349 GSM3503183 GSM3503183: D31_130_T1_20180323; Neisseria gonorrhoeae; ssRNA-seq SRP172735 PRJNA508744 SRS4110665 SAMN10526866 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503183 GSM3503183 GEO Accession GSM3503183 SRX5100350 GSM3503184 GSM3503184: D31_3X130_T1_20180323; Neisseria gonorrhoeae; ssRNA-seq SRP172735 PRJNA508744 SRS4110666 SAMN10526865 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503184 GSM3503184 GEO Accession GSM3503184 SRX5100351 GSM3503185 GSM3503185: D31_PMN_130_T0_20180323; Neisseria gonorrhoeae; Homo sapiens; ssRNA-seq SRP172735 PRJNA508744 SRS4110667 SAMN10526864 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503185 GSM3503185 GEO Accession GSM3503185 SRX5100352 GSM3503186 GSM3503186: D31_PMN_130_T1_20180323; Neisseria gonorrhoeae; Homo sapiens; ssRNA-seq SRP172735 PRJNA508744 SRS4110668 SAMN10526862 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503186 GSM3503186 GEO Accession GSM3503186 SRX5100353 GSM3503187 GSM3503187: D31_PMN_3X130_T0_20180323; Neisseria gonorrhoeae; Homo sapiens; ssRNA-seq SRP172735 PRJNA508744 SRS4110669 SAMN10526861 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503187 GSM3503187 GEO Accession GSM3503187 SRX5100354 GSM3503188 GSM3503188: D31_PMN_3X130_T1_20180323; Neisseria gonorrhoeae; Homo sapiens; ssRNA-seq SRP172735 PRJNA508744 SRS4110670 SAMN10526860 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503188 GSM3503188 GEO Accession GSM3503188 SRX5100355 GSM3503189 GSM3503189: D31_PMN_H041_T0_20180323; Neisseria gonorrhoeae; Homo sapiens; ssRNA-seq SRP172735 PRJNA508744 SRS4110671 SAMN10526859 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503189 GSM3503189 GEO Accession GSM3503189 SRX5100356 GSM3503190 GSM3503190: D31_PMN_H041_T1_20180323; Neisseria gonorrhoeae; Homo sapiens; ssRNA-seq SRP172735 PRJNA508744 SRS4110672 SAMN10526902 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503190 GSM3503190 GEO Accession GSM3503190 SRX5100357 GSM3503191 GSM3503191: D5_130_T1_20180206; Neisseria gonorrhoeae; ssRNA-seq SRP172735 PRJNA508744 SRS4110673 SAMN10526901 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503191 GSM3503191 GEO Accession GSM3503191 SRX5100358 GSM3503192 GSM3503192: D5_3X130_T1_20180206; Neisseria gonorrhoeae; ssRNA-seq SRP172735 PRJNA508744 SRS4110674 SAMN10526900 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503192 GSM3503192 GEO Accession GSM3503192 SRX5100359 GSM3503193 GSM3503193: D5_H041_T1_20180206; Neisseria gonorrhoeae; ssRNA-seq SRP172735 PRJNA508744 SRS4110675 SAMN10526899 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503193 GSM3503193 GEO Accession GSM3503193 SRX5100360 GSM3503194 GSM3503194: D5_PMN_130_T0_20180206; Neisseria gonorrhoeae; Homo sapiens; ssRNA-seq SRP172735 PRJNA508744 SRS4110676 SAMN10526897 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503194 GSM3503194 GEO Accession GSM3503194 SRX5100361 GSM3503195 GSM3503195: D5_PMN_130_T1_20180206; Neisseria gonorrhoeae; Homo sapiens; ssRNA-seq SRP172735 PRJNA508744 SRS4110677 SAMN10526896 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503195 GSM3503195 GEO Accession GSM3503195 SRX5100362 GSM3503196 GSM3503196: D5_PMN_3X130_T0_20180206; Neisseria gonorrhoeae; Homo sapiens; ssRNA-seq SRP172735 PRJNA508744 SRS4110678 SAMN10526895 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503196 GSM3503196 GEO Accession GSM3503196 SRX5100363 GSM3503197 GSM3503197: D5_PMN_3X130_T1_20180206; Neisseria gonorrhoeae; Homo sapiens; ssRNA-seq SRP172735 PRJNA508744 SRS4110679 SAMN10526894 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503197 GSM3503197 GEO Accession GSM3503197 SRX5100364 GSM3503198 GSM3503198: D5_PMN_H041_T0_20180206; Neisseria gonorrhoeae; Homo sapiens; ssRNA-seq SRP172735 PRJNA508744 SRS4110680 SAMN10526893 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503198 GSM3503198 GEO Accession GSM3503198 SRX5100365 GSM3503199 GSM3503199: D5_PMN_H041_T1_20180206; Neisseria gonorrhoeae; Homo sapiens; ssRNA-seq SRP172735 PRJNA508744 SRS4110681 SAMN10526892 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503199 GSM3503199 GEO Accession GSM3503199 SRX5100366 GSM3503200 GSM3503200: D55_130_T1_20180201; Neisseria gonorrhoeae; ssRNA-seq SRP172735 PRJNA508744 SRS4110682 SAMN10526891 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503200 GSM3503200 GEO Accession GSM3503200 SRX5100367 GSM3503201 GSM3503201: D55_3X130_T1_20180201; Neisseria gonorrhoeae; ssRNA-seq SRP172735 PRJNA508744 SRS4110683 SAMN10526890 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503201 GSM3503201 GEO Accession GSM3503201 SRX5100368 GSM3503202 GSM3503202: D55_H041_T1_20180201; Neisseria gonorrhoeae; ssRNA-seq SRP172735 PRJNA508744 SRS4110684 SAMN10526889 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503202 GSM3503202 GEO Accession GSM3503202 SRX5100369 GSM3503203 GSM3503203: D55_PMN_130_T0_20180201; Neisseria gonorrhoeae; Homo sapiens; ssRNA-seq SRP172735 PRJNA508744 SRS4110685 SAMN10526869 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503203 GSM3503203 GEO Accession GSM3503203 SRX5100370 GSM3503204 GSM3503204: D55_PMN_130_T1_20180201; Neisseria gonorrhoeae; Homo sapiens; ssRNA-seq SRP172735 PRJNA508744 SRS4110686 SAMN10526885 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503204 GSM3503204 GEO Accession GSM3503204 SRX5100371 GSM3503205 GSM3503205: D55_PMN_3x130_T0_20180201; Neisseria gonorrhoeae; Homo sapiens; ssRNA-seq SRP172735 PRJNA508744 SRS4110687 SAMN10526884 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503205 GSM3503205 GEO Accession GSM3503205 SRX5100372 GSM3503206 GSM3503206: D55_PMN_3x130_T1_20180201; Neisseria gonorrhoeae; Homo sapiens; ssRNA-seq SRP172735 PRJNA508744 SRS4110688 SAMN10526883 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503206 GSM3503206 GEO Accession GSM3503206 SRX5100373 GSM3503207 GSM3503207: D55_PMN_H041_T0_20180201; Neisseria gonorrhoeae; Homo sapiens; ssRNA-seq SRP172735 PRJNA508744 SRS4110689 SAMN10526868 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503207 GSM3503207 GEO Accession GSM3503207 SRX5100374 GSM3503208 GSM3503208: D55_PMN_H041_T1_20180201; Neisseria gonorrhoeae; Homo sapiens; ssRNA-seq SRP172735 PRJNA508744 SRS4110690 SAMN10526867 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503208 GSM3503208 GEO Accession GSM3503208 SRX5100375 GSM3503209 GSM3503209: D6_130_T1_20180131; Neisseria gonorrhoeae; ssRNA-seq SRP172735 PRJNA508744 SRS4110691 SAMN10526887 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503209 GSM3503209 GEO Accession GSM3503209 SRX5100376 GSM3503210 GSM3503210: D6_H041_T1_20180131; Neisseria gonorrhoeae; ssRNA-seq SRP172735 PRJNA508744 SRS4110692 SAMN10526886 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503210 GSM3503210 GEO Accession GSM3503210 SRX5100377 GSM3503211 GSM3503211: D6_PMN_130_T0_20180131; Neisseria gonorrhoeae; Homo sapiens; ssRNA-seq SRP172735 PRJNA508744 SRS4110693 SAMN10526882 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503211 GSM3503211 GEO Accession GSM3503211 SRX5100378 GSM3503212 GSM3503212: D6_PMN_130_T1_20180131; Neisseria gonorrhoeae; Homo sapiens; ssRNA-seq SRP172735 PRJNA508744 SRS4110694 SAMN10526881 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503212 GSM3503212 GEO Accession GSM3503212 SRX5100379 GSM3503213 GSM3503213: D6_PMN_H041_T0_20180131; Neisseria gonorrhoeae; Homo sapiens; ssRNA-seq SRP172735 PRJNA508744 SRS4110695 SAMN10526880 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503213 GSM3503213 GEO Accession GSM3503213 SRX5100380 GSM3503214 GSM3503214: D6_PMN_H041_T1_20180131; Neisseria gonorrhoeae; Homo sapiens; ssRNA-seq SRP172735 PRJNA508744 SRS4110696 SAMN10526879 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503214 GSM3503214 GEO Accession GSM3503214 SRX5100381 GSM3503215 GSM3503215: D60_130_T1_20180208; Neisseria gonorrhoeae; ssRNA-seq SRP172735 PRJNA508744 SRS4110697 SAMN10526878 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503215 GSM3503215 GEO Accession GSM3503215 SRX5100382 GSM3503216 GSM3503216: D60_3X130_T1_20180208; Neisseria gonorrhoeae; ssRNA-seq SRP172735 PRJNA508744 SRS4110698 SAMN10526877 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503216 GSM3503216 GEO Accession GSM3503216 SRX5100383 GSM3503217 GSM3503217: D60_H041_T1_20180208; Neisseria gonorrhoeae; ssRNA-seq SRP172735 PRJNA508744 SRS4110699 SAMN10526876 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503217 GSM3503217 GEO Accession GSM3503217 SRX5100384 GSM3503218 GSM3503218: D60_PMN_130_T0_20180208; Neisseria gonorrhoeae; Homo sapiens; ssRNA-seq SRP172735 PRJNA508744 SRS4110700 SAMN10526875 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503218 GSM3503218 GEO Accession GSM3503218 SRX5100385 GSM3503219 GSM3503219: D60_PMN_130_T1_20180208; Neisseria gonorrhoeae; Homo sapiens; ssRNA-seq SRP172735 PRJNA508744 SRS4110701 SAMN10526874 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503219 GSM3503219 GEO Accession GSM3503219 SRX5100386 GSM3503220 GSM3503220: D60_PMN_3X130_T0_20180208; Neisseria gonorrhoeae; Homo sapiens; ssRNA-seq SRP172735 PRJNA508744 SRS4110702 SAMN10526873 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503220 GSM3503220 GEO Accession GSM3503220 SRX5100387 GSM3503221 GSM3503221: D60_PMN_3X130_T1_20180208; Neisseria gonorrhoeae; Homo sapiens; ssRNA-seq SRP172735 PRJNA508744 SRS4110703 SAMN10526872 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503221 GSM3503221 GEO Accession GSM3503221 SRX5100388 GSM3503222 GSM3503222: D60_PMN_H041_T0_20180208; Neisseria gonorrhoeae; Homo sapiens; ssRNA-seq SRP172735 PRJNA508744 SRS4110704 SAMN10526871 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503222 GSM3503222 GEO Accession GSM3503222 SRX5100389 GSM3503223 GSM3503223: D60_PMN_H041_T1_20180208; Neisseria gonorrhoeae; Homo sapiens; ssRNA-seq SRP172735 PRJNA508744 SRS4110705 SAMN10526870 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 303503223 GSM3503223 GEO Accession GSM3503223 SRX7119573 GSM4155497 GSM4155497: D55_130_Azit_20181106; Neisseria gonorrhoeae; RNA-Seq SRP172735 PRJNA508744 SRS5629714 GSM4155497 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155497 GSM4155497 GEO Accession GSM4155497 SRX7119574 GSM4155498 GSM4155498: D55_130_Ceft_20181106; Neisseria gonorrhoeae; RNA-Seq SRP172735 PRJNA508744 SRS5629715 GSM4155498 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155498 GSM4155498 GEO Accession GSM4155498 SRX7119575 GSM4155499 GSM4155499: D55_130_Gent_20181106; Neisseria gonorrhoeae; RNA-Seq SRP172735 PRJNA508744 SRS5629716 GSM4155499 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155499 GSM4155499 GEO Accession GSM4155499 SRX7119576 GSM4155500 GSM4155500: D55_130_T1_20181106; Neisseria gonorrhoeae; RNA-Seq SRP172735 PRJNA508744 SRS5629717 GSM4155500 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155500 GSM4155500 GEO Accession GSM4155500 SRX7119577 GSM4155501 GSM4155501: D55_3X130_Azit_20190129; Neisseria gonorrhoeae; RNA-Seq SRP172735 PRJNA508744 SRS5629718 GSM4155501 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155501 GSM4155501 GEO Accession GSM4155501 SRX7119578 GSM4155502 GSM4155502: D55_3X130_Ceft_20190129; Neisseria gonorrhoeae; RNA-Seq SRP172735 PRJNA508744 SRS5629719 GSM4155502 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155502 GSM4155502 GEO Accession GSM4155502 SRX7119579 GSM4155503 GSM4155503: D55_3X130_Gent_20190129; Neisseria gonorrhoeae; RNA-Seq SRP172735 PRJNA508744 SRS5629720 GSM4155503 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155503 GSM4155503 GEO Accession GSM4155503 SRX7119580 GSM4155504 GSM4155504: D55_3X130_T1_20190129; Neisseria gonorrhoeae; RNA-Seq SRP172735 PRJNA508744 SRS5629721 GSM4155504 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155504 GSM4155504 GEO Accession GSM4155504 SRX7119581 GSM4155505 GSM4155505: D55_H041_Azit_20190110; Neisseria gonorrhoeae; RNA-Seq SRP172735 PRJNA508744 SRS5629722 GSM4155505 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155505 GSM4155505 GEO Accession GSM4155505 SRX7119582 GSM4155506 GSM4155506: D55_H041_Ceft_20190110; Neisseria gonorrhoeae; RNA-Seq SRP172735 PRJNA508744 SRS5629723 GSM4155506 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155506 GSM4155506 GEO Accession GSM4155506 SRX7119583 GSM4155507 GSM4155507: D55_H041_Gent_20190110; Neisseria gonorrhoeae; RNA-Seq SRP172735 PRJNA508744 SRS5629724 GSM4155507 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155507 GSM4155507 GEO Accession GSM4155507 SRX7119584 GSM4155508 GSM4155508: D55_H041_T1_20190110; Neisseria gonorrhoeae; RNA-Seq SRP172735 PRJNA508744 SRS5629725 GSM4155508 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155508 GSM4155508 GEO Accession GSM4155508 SRX7119585 GSM4155509 GSM4155509: D55_PMN_130_Azit_T0_20181106; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629726 GSM4155509 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155509 GSM4155509 GEO Accession GSM4155509 SRX7119586 GSM4155510 GSM4155510: D55_PMN_130_Azit_T1_20181106; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629727 GSM4155510 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155510 GSM4155510 GEO Accession GSM4155510 SRX7119587 GSM4155511 GSM4155511: D55_PMN_130_Ceft_T0_20181106; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629728 GSM4155511 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155511 GSM4155511 GEO Accession GSM4155511 SRX7119588 GSM4155512 GSM4155512: D55_PMN_130_Ceft_T1_20181106; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629729 GSM4155512 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155512 GSM4155512 GEO Accession GSM4155512 SRX7119589 GSM4155513 GSM4155513: D55_PMN_130_Gent_T0_20181106; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629730 GSM4155513 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155513 GSM4155513 GEO Accession GSM4155513 SRX7119590 GSM4155514 GSM4155514: D55_PMN_130_Gent_T1_20181106; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629731 GSM4155514 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155514 GSM4155514 GEO Accession GSM4155514 SRX7119591 GSM4155515 GSM4155515: D55_PMN_130_T0_20181106; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629732 GSM4155515 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155515 GSM4155515 GEO Accession GSM4155515 SRX7119592 GSM4155516 GSM4155516: D55_PMN_130_T1_20181106; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629733 GSM4155516 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155516 GSM4155516 GEO Accession GSM4155516 SRX7119593 GSM4155517 GSM4155517: D55_PMN_3X130_Azit_T0_20190129; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629734 GSM4155517 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155517 GSM4155517 GEO Accession GSM4155517 SRX7119594 GSM4155518 GSM4155518: D55_PMN_3X130_Azit_T1_20190129; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629735 GSM4155518 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155518 GSM4155518 GEO Accession GSM4155518 SRX7119595 GSM4155519 GSM4155519: D55_PMN_3X130_Ceft_T0_20190129; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629736 GSM4155519 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155519 GSM4155519 GEO Accession GSM4155519 SRX7119596 GSM4155520 GSM4155520: D55_PMN_3X130_Ceft_T1_20190129; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629737 GSM4155520 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155520 GSM4155520 GEO Accession GSM4155520 SRX7119597 GSM4155521 GSM4155521: D55_PMN_3X130_Gent_T0_20190129; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629738 GSM4155521 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155521 GSM4155521 GEO Accession GSM4155521 SRX7119598 GSM4155522 GSM4155522: D55_PMN_3X130_Gent_T1_20190129; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629739 GSM4155522 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155522 GSM4155522 GEO Accession GSM4155522 SRX7119599 GSM4155523 GSM4155523: D55_PMN_3X130_T0_20190129; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629740 GSM4155523 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155523 GSM4155523 GEO Accession GSM4155523 SRX7119600 GSM4155524 GSM4155524: D55_PMN_3X130_T1_20190129; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629741 GSM4155524 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155524 GSM4155524 GEO Accession GSM4155524 SRX7119601 GSM4155525 GSM4155525: D55_PMN_alone_T0_20180920; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629742 GSM4155525 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155525 GSM4155525 GEO Accession GSM4155525 SRX7119602 GSM4155526 GSM4155526: D55_PMN_alone_T0_20190416; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629743 GSM4155526 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155526 GSM4155526 GEO Accession GSM4155526 SRX7119603 GSM4155527 GSM4155527: D55_PMN_alone_T1_20180920; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629744 GSM4155527 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155527 GSM4155527 GEO Accession GSM4155527 SRX7119604 GSM4155528 GSM4155528: D55_PMN_alone_T1_20190416; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629745 GSM4155528 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155528 GSM4155528 GEO Accession GSM4155528 SRX7119605 GSM4155529 GSM4155529: D55_PMN_H041_Azit_T0_20190110; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629746 GSM4155529 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155529 GSM4155529 GEO Accession GSM4155529 SRX7119606 GSM4155530 GSM4155530: D55_PMN_H041_Azit_T1_20190110; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629747 GSM4155530 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155530 GSM4155530 GEO Accession GSM4155530 SRX7119607 GSM4155531 GSM4155531: D55_PMN_H041_Ceft_T0_20190110; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629748 GSM4155531 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155531 GSM4155531 GEO Accession GSM4155531 SRX7119608 GSM4155532 GSM4155532: D55_PMN_H041_Ceft_T1_20190110; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629749 GSM4155532 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155532 GSM4155532 GEO Accession GSM4155532 SRX7119609 GSM4155533 GSM4155533: D55_PMN_H041_Gent_T0_20190110; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629750 GSM4155533 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155533 GSM4155533 GEO Accession GSM4155533 SRX7119610 GSM4155534 GSM4155534: D55_PMN_H041_Gent_T1_20190110; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629751 GSM4155534 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155534 GSM4155534 GEO Accession GSM4155534 SRX7119611 GSM4155535 GSM4155535: D55_PMN_H041_T0_20190110; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629752 GSM4155535 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155535 GSM4155535 GEO Accession GSM4155535 SRX7119612 GSM4155536 GSM4155536: D55_PMN_H041_T1_20190110; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629753 GSM4155536 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155536 GSM4155536 GEO Accession GSM4155536 SRX7119613 GSM4155537 GSM4155537: D6_130_Azit_20181108; Neisseria gonorrhoeae; RNA-Seq SRP172735 PRJNA508744 SRS5629754 GSM4155537 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155537 GSM4155537 GEO Accession GSM4155537 SRX7119614 GSM4155538 GSM4155538: D6_130_Ceft_20181108; Neisseria gonorrhoeae; RNA-Seq SRP172735 PRJNA508744 SRS5629755 GSM4155538 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155538 GSM4155538 GEO Accession GSM4155538 SRX7119615 GSM4155539 GSM4155539: D6_130_Gent_20181108; Neisseria gonorrhoeae; RNA-Seq SRP172735 PRJNA508744 SRS5629756 GSM4155539 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155539 GSM4155539 GEO Accession GSM4155539 SRX7119616 GSM4155540 GSM4155540: D6_130_T1_20181108; Neisseria gonorrhoeae; RNA-Seq SRP172735 PRJNA508744 SRS5629757 GSM4155540 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155540 GSM4155540 GEO Accession GSM4155540 SRX7119617 GSM4155541 GSM4155541: D6_3X130_Azit_20190307; Neisseria gonorrhoeae; RNA-Seq SRP172735 PRJNA508744 SRS5629758 GSM4155541 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155541 GSM4155541 GEO Accession GSM4155541 SRX7119618 GSM4155542 GSM4155542: D6_3X130_Azit_20190619; Neisseria gonorrhoeae; RNA-Seq SRP172735 PRJNA508744 SRS5629759 GSM4155542 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155542 GSM4155542 GEO Accession GSM4155542 SRX7119619 GSM4155543 GSM4155543: D6_3X130_Ceft_20190307; Neisseria gonorrhoeae; RNA-Seq SRP172735 PRJNA508744 SRS5629760 GSM4155543 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155543 GSM4155543 GEO Accession GSM4155543 SRX7119620 GSM4155544 GSM4155544: D6_3X130_Gent_20190307; Neisseria gonorrhoeae; RNA-Seq SRP172735 PRJNA508744 SRS5629761 GSM4155544 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155544 GSM4155544 GEO Accession GSM4155544 SRX7119621 GSM4155545 GSM4155545: D6_3X130_T1_20180802; Neisseria gonorrhoeae; RNA-Seq SRP172735 PRJNA508744 SRS5629762 GSM4155545 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155545 GSM4155545 GEO Accession GSM4155545 SRX7119622 GSM4155546 GSM4155546: D6_3X130_T1_20190307; Neisseria gonorrhoeae; RNA-Seq SRP172735 PRJNA508744 SRS5629763 GSM4155546 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155546 GSM4155546 GEO Accession GSM4155546 SRX7119623 GSM4155547 GSM4155547: D6_H041_Azit_20190122; Neisseria gonorrhoeae; RNA-Seq SRP172735 PRJNA508744 SRS5629764 GSM4155547 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155547 GSM4155547 GEO Accession GSM4155547 SRX7119624 GSM4155548 GSM4155548: D6_H041_Ceft_20190122; Neisseria gonorrhoeae; RNA-Seq SRP172735 PRJNA508744 SRS5629765 GSM4155548 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155548 GSM4155548 GEO Accession GSM4155548 SRX7119625 GSM4155549 GSM4155549: D6_H041_Gent_20190122; Neisseria gonorrhoeae; RNA-Seq SRP172735 PRJNA508744 SRS5629766 GSM4155549 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155549 GSM4155549 GEO Accession GSM4155549 SRX7119626 GSM4155550 GSM4155550: D6_H041_T1_20190122; Neisseria gonorrhoeae; RNA-Seq SRP172735 PRJNA508744 SRS5629767 GSM4155550 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155550 GSM4155550 GEO Accession GSM4155550 SRX7119627 GSM4155551 GSM4155551: D6_PMN_130_Azit_T0_20181108; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629768 GSM4155551 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155551 GSM4155551 GEO Accession GSM4155551 SRX7119628 GSM4155552 GSM4155552: D6_PMN_130_Azit_T1_20181108; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629769 GSM4155552 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155552 GSM4155552 GEO Accession GSM4155552 SRX7119629 GSM4155553 GSM4155553: D6_PMN_130_Ceft_T0_20181108; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629770 GSM4155553 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155553 GSM4155553 GEO Accession GSM4155553 SRX7119630 GSM4155554 GSM4155554: D6_PMN_130_Ceft_T1_20181108; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629771 GSM4155554 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155554 GSM4155554 GEO Accession GSM4155554 SRX7119631 GSM4155555 GSM4155555: D6_PMN_130_Gent_T0_20181108; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629772 GSM4155555 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155555 GSM4155555 GEO Accession GSM4155555 SRX7119632 GSM4155556 GSM4155556: D6_PMN_130_Gent_T1_20181108; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629773 GSM4155556 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155556 GSM4155556 GEO Accession GSM4155556 SRX7119633 GSM4155557 GSM4155557: D6_PMN_130_T0_20181108; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629774 GSM4155557 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155557 GSM4155557 GEO Accession GSM4155557 SRX7119634 GSM4155558 GSM4155558: D6_PMN_130_T1_20181108; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629775 GSM4155558 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155558 GSM4155558 GEO Accession GSM4155558 SRX7119635 GSM4155559 GSM4155559: D6_PMN_3X130_Azit_T0_20190307; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629776 GSM4155559 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155559 GSM4155559 GEO Accession GSM4155559 SRX7119636 GSM4155560 GSM4155560: D6_PMN_3X130_Azit_T0_20190619; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629777 GSM4155560 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155560 GSM4155560 GEO Accession GSM4155560 SRX7119637 GSM4155561 GSM4155561: D6_PMN_3X130_Azit_T1_20190307; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629778 GSM4155561 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155561 GSM4155561 GEO Accession GSM4155561 SRX7119638 GSM4155562 GSM4155562: D6_PMN_3X130_Azit_T1_20190619; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629779 GSM4155562 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155562 GSM4155562 GEO Accession GSM4155562 SRX7119639 GSM4155563 GSM4155563: D6_PMN_3X130_Ceft_T0_20190307; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629780 GSM4155563 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155563 GSM4155563 GEO Accession GSM4155563 SRX7119640 GSM4155564 GSM4155564: D6_PMN_3X130_Ceft_T1_20190307; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629781 GSM4155564 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155564 GSM4155564 GEO Accession GSM4155564 SRX7119641 GSM4155565 GSM4155565: D6_PMN_3X130_Gent_T0_20190307; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629782 GSM4155565 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155565 GSM4155565 GEO Accession GSM4155565 SRX7119642 GSM4155566 GSM4155566: D6_PMN_3X130_Gent_T1_20190307; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629783 GSM4155566 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155566 GSM4155566 GEO Accession GSM4155566 SRX7119643 GSM4155567 GSM4155567: D6_PMN_3X130_T0_20180802; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629784 GSM4155567 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155567 GSM4155567 GEO Accession GSM4155567 SRX7119644 GSM4155568 GSM4155568: D6_PMN_3X130_T0_20190307; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629785 GSM4155568 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155568 GSM4155568 GEO Accession GSM4155568 SRX7119645 GSM4155569 GSM4155569: D6_PMN_3X130_T1_20180802; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629786 GSM4155569 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155569 GSM4155569 GEO Accession GSM4155569 SRX7119646 GSM4155570 GSM4155570: D6_PMN_3X130_T1_20190307; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629787 GSM4155570 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155570 GSM4155570 GEO Accession GSM4155570 SRX7119647 GSM4155571 GSM4155571: D6_PMN_alone_T0_20180802; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629788 GSM4155571 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155571 GSM4155571 GEO Accession GSM4155571 SRX7119648 GSM4155572 GSM4155572: D6_PMN_alone_T0_20190416; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629789 GSM4155572 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155572 GSM4155572 GEO Accession GSM4155572 SRX7119649 GSM4155573 GSM4155573: D6_PMN_alone_T1_20180802; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629790 GSM4155573 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155573 GSM4155573 GEO Accession GSM4155573 SRX7119650 GSM4155574 GSM4155574: D6_PMN_alone_T1_20190416; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629791 GSM4155574 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155574 GSM4155574 GEO Accession GSM4155574 SRX7119651 GSM4155575 GSM4155575: D6_PMN_H041_Azit_T0_20190122; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629792 GSM4155575 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155575 GSM4155575 GEO Accession GSM4155575 SRX7119652 GSM4155576 GSM4155576: D6_PMN_H041_Azit_T1_20190122; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629793 GSM4155576 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155576 GSM4155576 GEO Accession GSM4155576 SRX7119653 GSM4155577 GSM4155577: D6_PMN_H041_Ceft_T0_20190122; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629794 GSM4155577 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155577 GSM4155577 GEO Accession GSM4155577 SRX7119654 GSM4155578 GSM4155578: D6_PMN_H041_Ceft_T1_20190122; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629795 GSM4155578 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155578 GSM4155578 GEO Accession GSM4155578 SRX7119655 GSM4155579 GSM4155579: D6_PMN_H041_Gent_T0_20190122; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629796 GSM4155579 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155579 GSM4155579 GEO Accession GSM4155579 SRX7119656 GSM4155580 GSM4155580: D6_PMN_H041_Gent_T1_20190122; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629797 GSM4155580 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155580 GSM4155580 GEO Accession GSM4155580 SRX7119657 GSM4155581 GSM4155581: D6_PMN_H041_T0_20190122; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629798 GSM4155581 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155581 GSM4155581 GEO Accession GSM4155581 SRX7119658 GSM4155582 GSM4155582: D6_PMN_H041_T1_20190122; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629799 GSM4155582 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155582 GSM4155582 GEO Accession GSM4155582 SRX7119659 GSM4155583 GSM4155583: D60_130_Azit_20181113; Neisseria gonorrhoeae; RNA-Seq SRP172735 PRJNA508744 SRS5629800 GSM4155583 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155583 GSM4155583 GEO Accession GSM4155583 SRX7119660 GSM4155584 GSM4155584: D60_130_Ceft_20181113; Neisseria gonorrhoeae; RNA-Seq SRP172735 PRJNA508744 SRS5629801 GSM4155584 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155584 GSM4155584 GEO Accession GSM4155584 SRX7119661 GSM4155585 GSM4155585: D60_130_Gent_20181113; Neisseria gonorrhoeae; RNA-Seq SRP172735 PRJNA508744 SRS5629802 GSM4155585 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155585 GSM4155585 GEO Accession GSM4155585 SRX7119662 GSM4155586 GSM4155586: D60_130_T1_20181113; Neisseria gonorrhoeae; RNA-Seq SRP172735 PRJNA508744 SRS5629803 GSM4155586 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155586 GSM4155586 GEO Accession GSM4155586 SRX7119663 GSM4155587 GSM4155587: D60_3X130_Azit_20190305; Neisseria gonorrhoeae; RNA-Seq SRP172735 PRJNA508744 SRS5629804 GSM4155587 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155587 GSM4155587 GEO Accession GSM4155587 SRX7119664 GSM4155588 GSM4155588: D60_3X130_Ceft_20190305; Neisseria gonorrhoeae; RNA-Seq SRP172735 PRJNA508744 SRS5629805 GSM4155588 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155588 GSM4155588 GEO Accession GSM4155588 SRX7119665 GSM4155589 GSM4155589: D60_3X130_Gent_20190305; Neisseria gonorrhoeae; RNA-Seq SRP172735 PRJNA508744 SRS5629806 GSM4155589 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155589 GSM4155589 GEO Accession GSM4155589 SRX7119666 GSM4155590 GSM4155590: D60_3X130_T1_20190305; Neisseria gonorrhoeae; RNA-Seq SRP172735 PRJNA508744 SRS5629807 GSM4155590 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155590 GSM4155590 GEO Accession GSM4155590 SRX7119667 GSM4155591 GSM4155591: D60_H041_Azit_20190709; Neisseria gonorrhoeae; RNA-Seq SRP172735 PRJNA508744 SRS5629808 GSM4155591 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155591 GSM4155591 GEO Accession GSM4155591 SRX7119668 GSM4155592 GSM4155592: D60_H041_Ceft_20190709; Neisseria gonorrhoeae; RNA-Seq SRP172735 PRJNA508744 SRS5629809 GSM4155592 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155592 GSM4155592 GEO Accession GSM4155592 SRX7119669 GSM4155593 GSM4155593: D60_H041_Gent_20190709; Neisseria gonorrhoeae; RNA-Seq SRP172735 PRJNA508744 SRS5629810 GSM4155593 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155593 GSM4155593 GEO Accession GSM4155593 SRX7119670 GSM4155594 GSM4155594: D60_H041_T1_20190709; Neisseria gonorrhoeae; RNA-Seq SRP172735 PRJNA508744 SRS5629811 GSM4155594 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155594 GSM4155594 GEO Accession GSM4155594 SRX7119671 GSM4155595 GSM4155595: D60_PMN_130_Azit_T0_20181113; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629812 GSM4155595 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155595 GSM4155595 GEO Accession GSM4155595 SRX7119672 GSM4155596 GSM4155596: D60_PMN_130_Azit_T1_20181113; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629813 GSM4155596 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155596 GSM4155596 GEO Accession GSM4155596 SRX7119673 GSM4155597 GSM4155597: D60_PMN_130_Ceft_T0_20181113; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629814 GSM4155597 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155597 GSM4155597 GEO Accession GSM4155597 SRX7119674 GSM4155598 GSM4155598: D60_PMN_130_Ceft_T1_20181113; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629815 GSM4155598 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155598 GSM4155598 GEO Accession GSM4155598 SRX7119675 GSM4155599 GSM4155599: D60_PMN_130_Gent_T0_20181113; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629816 GSM4155599 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155599 GSM4155599 GEO Accession GSM4155599 SRX7119676 GSM4155600 GSM4155600: D60_PMN_130_Gent_T1_20181113; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629817 GSM4155600 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155600 GSM4155600 GEO Accession GSM4155600 SRX7119677 GSM4155601 GSM4155601: D60_PMN_130_T0_20181113; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629818 GSM4155601 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155601 GSM4155601 GEO Accession GSM4155601 SRX7119678 GSM4155602 GSM4155602: D60_PMN_130_T1_20181113; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629819 GSM4155602 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155602 GSM4155602 GEO Accession GSM4155602 SRX7119679 GSM4155603 GSM4155603: D60_PMN_3X130_Azit_T0_20190305; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629820 GSM4155603 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155603 GSM4155603 GEO Accession GSM4155603 SRX7119680 GSM4155604 GSM4155604: D60_PMN_3X130_Azit_T1_20190305; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629821 GSM4155604 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155604 GSM4155604 GEO Accession GSM4155604 SRX7119681 GSM4155605 GSM4155605: D60_PMN_3X130_Ceft_T0_20190305; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629822 GSM4155605 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155605 GSM4155605 GEO Accession GSM4155605 SRX7119682 GSM4155606 GSM4155606: D60_PMN_3X130_Ceft_T0_20190730; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629823 GSM4155606 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155606 GSM4155606 GEO Accession GSM4155606 SRX7119683 GSM4155607 GSM4155607: D60_PMN_3X130_Ceft_T1_20190305; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629824 GSM4155607 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155607 GSM4155607 GEO Accession GSM4155607 SRX7119684 GSM4155608 GSM4155608: D60_PMN_3X130_Ceft_T1_20190625; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629825 GSM4155608 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155608 GSM4155608 GEO Accession GSM4155608 SRX7119685 GSM4155609 GSM4155609: D60_PMN_3X130_Ceft_T1_20190730; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629826 GSM4155609 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155609 GSM4155609 GEO Accession GSM4155609 SRX7119686 GSM4155610 GSM4155610: D60_PMN_3X130_Gent_T0_20190305; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629827 GSM4155610 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155610 GSM4155610 GEO Accession GSM4155610 SRX7119687 GSM4155611 GSM4155611: D60_PMN_3X130_Gent_T1_20190305; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629828 GSM4155611 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155611 GSM4155611 GEO Accession GSM4155611 SRX7119688 GSM4155612 GSM4155612: D60_PMN_3X130_T0_20190305; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629829 GSM4155612 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155612 GSM4155612 GEO Accession GSM4155612 SRX7119689 GSM4155613 GSM4155613: D60_PMN_3X130_T1_20190305; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629830 GSM4155613 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155613 GSM4155613 GEO Accession GSM4155613 SRX7119690 GSM4155614 GSM4155614: D60_PMN_alone_T0_20190416; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629831 GSM4155614 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155614 GSM4155614 GEO Accession GSM4155614 SRX7119691 GSM4155615 GSM4155615: D60_PMN_alone_T0_20190730; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629832 GSM4155615 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155615 GSM4155615 GEO Accession GSM4155615 SRX7119692 GSM4155616 GSM4155616: D60_PMN_alone_T1_20190416; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629833 GSM4155616 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155616 GSM4155616 GEO Accession GSM4155616 SRX7119693 GSM4155617 GSM4155617: D60_PMN_H041_Azit_T0_20190709; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629834 GSM4155617 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155617 GSM4155617 GEO Accession GSM4155617 SRX7119694 GSM4155618 GSM4155618: D60_PMN_H041_Azit_T1_20190709; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629835 GSM4155618 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155618 GSM4155618 GEO Accession GSM4155618 SRX7119695 GSM4155619 GSM4155619: D60_PMN_H041_Ceft_T0_20190709; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629836 GSM4155619 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155619 GSM4155619 GEO Accession GSM4155619 SRX7119696 GSM4155620 GSM4155620: D60_PMN_H041_Ceft_T1_20190709; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629837 GSM4155620 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155620 GSM4155620 GEO Accession GSM4155620 SRX7119697 GSM4155621 GSM4155621: D60_PMN_H041_Gent_T0_20190709; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629838 GSM4155621 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155621 GSM4155621 GEO Accession GSM4155621 SRX7119698 GSM4155622 GSM4155622: D60_PMN_H041_Gent_T1_20190709; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629839 GSM4155622 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155622 GSM4155622 GEO Accession GSM4155622 SRX7119699 GSM4155623 GSM4155623: D60_PMN_H041_T0_20181212; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629840 GSM4155623 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155623 GSM4155623 GEO Accession GSM4155623 SRX7119700 GSM4155624 GSM4155624: D60_PMN_H041_T0_20190709; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629841 GSM4155624 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155624 GSM4155624 GEO Accession GSM4155624 SRX7119701 GSM4155625 GSM4155625: D60_PMN_H041_T1_20181212; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629842 GSM4155625 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155625 GSM4155625 GEO Accession GSM4155625 SRX7119702 GSM4155626 GSM4155626: D60_PMN_H041_T1_20190709; Neisseria gonorrhoeae; Homo sapiens; RNA-Seq SRP172735 PRJNA508744 SRS5629843 GSM4155626 RNA-Seq TRANSCRIPTOMIC cDNA At indicated times, samples were placed on ice. Bacteria alone were collected into microcentrifuge tubes, pelleted, and stored in RNAprotect at -80C. Supernatants were discarded from neutrophil containing samples, RNA protect was added, and samples were stored at -80C. Samples were exposed to EDTA pre-extraction and during the lysis step. Extractions were performed using Qiagen's RNeasy extraction kit as per manufacturer's protocol. An additional Turbo DNase was performed after the final step of RNeasy protocol. Quality and quantity were determined using the Agilent 4200 TapeStation System. Strand specific RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304155626 GSM4155626 GEO Accession GSM4155626