ERS1672381 SAMEA103983213 367830 Staphylococcus aureus subsp. aureus USA300 Protocols: To monitor the global changes in gene expression of Staphylococcus aureus USA300 TCH1516 under hypochlorite stress by RNA-seq, cultivation was performed in Luria Bertani (LB) medium in triplicate at 37°C until cells have reached an optical density at 540 nm of 2.0. Cells were harvested by centrifugation, washed with Belitsky minimal medium (BMM) and adapted to BMM for one hour before exposure to 150 µM NaOCl stress. S. aureus cells of 3 replicate experiments were harvested before and 30 min after exposure to 150 µM NaOCl S. aureus cells were harvested before and 30 min after exposure to 150 µM NaOCl and disrupted in 3 mM EDTA/ 200 mM NaCl lysis buffer with a Precellys24 Ribolyzer. RNA isolation was performed using the phenol-chloroform-isoamylalcohol approach. After precipitation with 3 M sodium acetate and isopropanol, the total RNA was washed with cold ethanol and the pellet was solved in sterile water. Initially RNA quality was checked by Trinean Xpose (Gentbrugge,Belgium) and Agilent RNA Nano 6000 kit on Agilent 2100 Bioanalyzer (Agilent Technologies, Böblingen, Germany). Samples contaminated with DNA were treated with DNase (Qiagen), cleaned as described above and rechecked by Xpose and Agilent Bioanalyzer. Finally RNA was free of DNA with an RNA Integrity Number (RIN) > 9 and rRNA Ratio [23s / 16s] > 1.5. Ribo-Zero rRNA Removal Kit (Bacteria) from Illumina (San Diego, CA, USA) was used to remove the ribosomal RNA molecules from the isolated total RNA. Removal of rRNA was checked by Agilent RNA Pico 6000 kit on Agilent 2100 Bioanalyzer (Agilent Technologies, Böblingen, Germany). RNA was free of detectable rRNA. TruSeq Stranded mRNA Library Prep Kit from Illumina (San Diego, CA, USA) was used to prepare cDNA libraries. ENA-FIRST-PUBLIC 2017-12-18T17:02:51Z ENA-LAST-UPDATE 2017-04-19T13:22:23Z External Id SAMEA103983213 INSDC center name Freie Universitat Berlin Institut fur Biologie-Mikrobiologie INSDC first public 2017-12-18T17:02:51Z INSDC last update 2017-04-19T13:22:23Z INSDC status public Submitter Id E-MTAB-5666:Staph_aureus_Co_I broker name ArrayExpress sample name E-MTAB-5666:Staph_aureus_Co_I scientific_name Staphylococcus aureus subsp. aureus USA300 ERS1672382 SAMEA103983214 367830 Staphylococcus aureus subsp. aureus USA300 Protocols: To monitor the global changes in gene expression of Staphylococcus aureus USA300 TCH1516 under hypochlorite stress by RNA-seq, cultivation was performed in Luria Bertani (LB) medium in triplicate at 37°C until cells have reached an optical density at 540 nm of 2.0. Cells were harvested by centrifugation, washed with Belitsky minimal medium (BMM) and adapted to BMM for one hour before exposure to 150 µM NaOCl stress. S. aureus cells of 3 replicate experiments were harvested before and 30 min after exposure to 150 µM NaOCl S. aureus cells were harvested before and 30 min after exposure to 150 µM NaOCl and disrupted in 3 mM EDTA/ 200 mM NaCl lysis buffer with a Precellys24 Ribolyzer. RNA isolation was performed using the phenol-chloroform-isoamylalcohol approach. After precipitation with 3 M sodium acetate and isopropanol, the total RNA was washed with cold ethanol and the pellet was solved in sterile water. Initially RNA quality was checked by Trinean Xpose (Gentbrugge,Belgium) and Agilent RNA Nano 6000 kit on Agilent 2100 Bioanalyzer (Agilent Technologies, Böblingen, Germany). Samples contaminated with DNA were treated with DNase (Qiagen), cleaned as described above and rechecked by Xpose and Agilent Bioanalyzer. Finally RNA was free of DNA with an RNA Integrity Number (RIN) > 9 and rRNA Ratio [23s / 16s] > 1.5. Ribo-Zero rRNA Removal Kit (Bacteria) from Illumina (San Diego, CA, USA) was used to remove the ribosomal RNA molecules from the isolated total RNA. Removal of rRNA was checked by Agilent RNA Pico 6000 kit on Agilent 2100 Bioanalyzer (Agilent Technologies, Böblingen, Germany). RNA was free of detectable rRNA. TruSeq Stranded mRNA Library Prep Kit from Illumina (San Diego, CA, USA) was used to prepare cDNA libraries. ENA-FIRST-PUBLIC 2017-12-18T17:02:51Z ENA-LAST-UPDATE 2017-04-19T13:22:23Z External Id SAMEA103983214 INSDC center name Freie Universitat Berlin Institut fur Biologie-Mikrobiologie INSDC first public 2017-12-18T17:02:51Z INSDC last update 2017-04-19T13:22:23Z INSDC status public Submitter Id E-MTAB-5666:Staph_aureus_Co_II broker name ArrayExpress sample name E-MTAB-5666:Staph_aureus_Co_II scientific_name Staphylococcus aureus subsp. aureus USA300 ERS1672383 SAMEA103983215 367830 Staphylococcus aureus subsp. aureus USA300 Protocols: To monitor the global changes in gene expression of Staphylococcus aureus USA300 TCH1516 under hypochlorite stress by RNA-seq, cultivation was performed in Luria Bertani (LB) medium in triplicate at 37°C until cells have reached an optical density at 540 nm of 2.0. Cells were harvested by centrifugation, washed with Belitsky minimal medium (BMM) and adapted to BMM for one hour before exposure to 150 µM NaOCl stress. S. aureus cells of 3 replicate experiments were harvested before and 30 min after exposure to 150 µM NaOCl S. aureus cells were harvested before and 30 min after exposure to 150 µM NaOCl and disrupted in 3 mM EDTA/ 200 mM NaCl lysis buffer with a Precellys24 Ribolyzer. RNA isolation was performed using the phenol-chloroform-isoamylalcohol approach. After precipitation with 3 M sodium acetate and isopropanol, the total RNA was washed with cold ethanol and the pellet was solved in sterile water. Initially RNA quality was checked by Trinean Xpose (Gentbrugge,Belgium) and Agilent RNA Nano 6000 kit on Agilent 2100 Bioanalyzer (Agilent Technologies, Böblingen, Germany). Samples contaminated with DNA were treated with DNase (Qiagen), cleaned as described above and rechecked by Xpose and Agilent Bioanalyzer. Finally RNA was free of DNA with an RNA Integrity Number (RIN) > 9 and rRNA Ratio [23s / 16s] > 1.5. Ribo-Zero rRNA Removal Kit (Bacteria) from Illumina (San Diego, CA, USA) was used to remove the ribosomal RNA molecules from the isolated total RNA. Removal of rRNA was checked by Agilent RNA Pico 6000 kit on Agilent 2100 Bioanalyzer (Agilent Technologies, Böblingen, Germany). RNA was free of detectable rRNA. TruSeq Stranded mRNA Library Prep Kit from Illumina (San Diego, CA, USA) was used to prepare cDNA libraries. ENA-FIRST-PUBLIC 2017-12-18T17:02:51Z ENA-LAST-UPDATE 2017-04-19T13:22:23Z External Id SAMEA103983215 INSDC center name Freie Universitat Berlin Institut fur Biologie-Mikrobiologie INSDC first public 2017-12-18T17:02:51Z INSDC last update 2017-04-19T13:22:23Z INSDC status public Submitter Id E-MTAB-5666:Staph_aureus_Co_III broker name ArrayExpress sample name E-MTAB-5666:Staph_aureus_Co_III scientific_name Staphylococcus aureus subsp. aureus USA300 ERS1672384 SAMEA103983216 367830 Staphylococcus aureus subsp. aureus USA300 Protocols: To monitor the global changes in gene expression of Staphylococcus aureus USA300 TCH1516 under hypochlorite stress by RNA-seq, cultivation was performed in Luria Bertani (LB) medium in triplicate at 37°C until cells have reached an optical density at 540 nm of 2.0. Cells were harvested by centrifugation, washed with Belitsky minimal medium (BMM) and adapted to BMM for one hour before exposure to 150 µM NaOCl stress. S. aureus cells of 3 replicate experiments were harvested before and 30 min after exposure to 150 µM NaOCl S. aureus cells were harvested before and 30 min after exposure to 150 µM NaOCl and disrupted in 3 mM EDTA/ 200 mM NaCl lysis buffer with a Precellys24 Ribolyzer. RNA isolation was performed using the phenol-chloroform-isoamylalcohol approach. After precipitation with 3 M sodium acetate and isopropanol, the total RNA was washed with cold ethanol and the pellet was solved in sterile water. Initially RNA quality was checked by Trinean Xpose (Gentbrugge,Belgium) and Agilent RNA Nano 6000 kit on Agilent 2100 Bioanalyzer (Agilent Technologies, Böblingen, Germany). Samples contaminated with DNA were treated with DNase (Qiagen), cleaned as described above and rechecked by Xpose and Agilent Bioanalyzer. Finally RNA was free of DNA with an RNA Integrity Number (RIN) > 9 and rRNA Ratio [23s / 16s] > 1.5. Ribo-Zero rRNA Removal Kit (Bacteria) from Illumina (San Diego, CA, USA) was used to remove the ribosomal RNA molecules from the isolated total RNA. Removal of rRNA was checked by Agilent RNA Pico 6000 kit on Agilent 2100 Bioanalyzer (Agilent Technologies, Böblingen, Germany). RNA was free of detectable rRNA. TruSeq Stranded mRNA Library Prep Kit from Illumina (San Diego, CA, USA) was used to prepare cDNA libraries. ENA-FIRST-PUBLIC 2017-12-18T17:02:51Z ENA-LAST-UPDATE 2017-04-19T13:22:23Z External Id SAMEA103983216 INSDC center name Freie Universitat Berlin Institut fur Biologie-Mikrobiologie INSDC first public 2017-12-18T17:02:51Z INSDC last update 2017-04-19T13:22:23Z INSDC status public Submitter Id E-MTAB-5666:Staph_aureus_NaOCl_I broker name ArrayExpress sample name E-MTAB-5666:Staph_aureus_NaOCl_I scientific_name Staphylococcus aureus subsp. aureus USA300 ERS1672385 SAMEA103983217 367830 Staphylococcus aureus subsp. aureus USA300 Protocols: To monitor the global changes in gene expression of Staphylococcus aureus USA300 TCH1516 under hypochlorite stress by RNA-seq, cultivation was performed in Luria Bertani (LB) medium in triplicate at 37°C until cells have reached an optical density at 540 nm of 2.0. Cells were harvested by centrifugation, washed with Belitsky minimal medium (BMM) and adapted to BMM for one hour before exposure to 150 µM NaOCl stress. S. aureus cells of 3 replicate experiments were harvested before and 30 min after exposure to 150 µM NaOCl S. aureus cells were harvested before and 30 min after exposure to 150 µM NaOCl and disrupted in 3 mM EDTA/ 200 mM NaCl lysis buffer with a Precellys24 Ribolyzer. RNA isolation was performed using the phenol-chloroform-isoamylalcohol approach. After precipitation with 3 M sodium acetate and isopropanol, the total RNA was washed with cold ethanol and the pellet was solved in sterile water. Initially RNA quality was checked by Trinean Xpose (Gentbrugge,Belgium) and Agilent RNA Nano 6000 kit on Agilent 2100 Bioanalyzer (Agilent Technologies, Böblingen, Germany). Samples contaminated with DNA were treated with DNase (Qiagen), cleaned as described above and rechecked by Xpose and Agilent Bioanalyzer. Finally RNA was free of DNA with an RNA Integrity Number (RIN) > 9 and rRNA Ratio [23s / 16s] > 1.5. Ribo-Zero rRNA Removal Kit (Bacteria) from Illumina (San Diego, CA, USA) was used to remove the ribosomal RNA molecules from the isolated total RNA. Removal of rRNA was checked by Agilent RNA Pico 6000 kit on Agilent 2100 Bioanalyzer (Agilent Technologies, Böblingen, Germany). RNA was free of detectable rRNA. TruSeq Stranded mRNA Library Prep Kit from Illumina (San Diego, CA, USA) was used to prepare cDNA libraries. ENA-FIRST-PUBLIC 2017-12-18T17:02:51Z ENA-LAST-UPDATE 2017-04-19T13:22:23Z External Id SAMEA103983217 INSDC center name Freie Universitat Berlin Institut fur Biologie-Mikrobiologie INSDC first public 2017-12-18T17:02:51Z INSDC last update 2017-04-19T13:22:23Z INSDC status public Submitter Id E-MTAB-5666:Staph_aureus_NaOCl_II broker name ArrayExpress sample name E-MTAB-5666:Staph_aureus_NaOCl_II scientific_name Staphylococcus aureus subsp. aureus USA300 ERS1672386 SAMEA103983218 367830 Staphylococcus aureus subsp. aureus USA300 Protocols: To monitor the global changes in gene expression of Staphylococcus aureus USA300 TCH1516 under hypochlorite stress by RNA-seq, cultivation was performed in Luria Bertani (LB) medium in triplicate at 37°C until cells have reached an optical density at 540 nm of 2.0. Cells were harvested by centrifugation, washed with Belitsky minimal medium (BMM) and adapted to BMM for one hour before exposure to 150 µM NaOCl stress. S. aureus cells of 3 replicate experiments were harvested before and 30 min after exposure to 150 µM NaOCl S. aureus cells were harvested before and 30 min after exposure to 150 µM NaOCl and disrupted in 3 mM EDTA/ 200 mM NaCl lysis buffer with a Precellys24 Ribolyzer. RNA isolation was performed using the phenol-chloroform-isoamylalcohol approach. After precipitation with 3 M sodium acetate and isopropanol, the total RNA was washed with cold ethanol and the pellet was solved in sterile water. Initially RNA quality was checked by Trinean Xpose (Gentbrugge,Belgium) and Agilent RNA Nano 6000 kit on Agilent 2100 Bioanalyzer (Agilent Technologies, Böblingen, Germany). Samples contaminated with DNA were treated with DNase (Qiagen), cleaned as described above and rechecked by Xpose and Agilent Bioanalyzer. Finally RNA was free of DNA with an RNA Integrity Number (RIN) > 9 and rRNA Ratio [23s / 16s] > 1.5. Ribo-Zero rRNA Removal Kit (Bacteria) from Illumina (San Diego, CA, USA) was used to remove the ribosomal RNA molecules from the isolated total RNA. Removal of rRNA was checked by Agilent RNA Pico 6000 kit on Agilent 2100 Bioanalyzer (Agilent Technologies, Böblingen, Germany). RNA was free of detectable rRNA. TruSeq Stranded mRNA Library Prep Kit from Illumina (San Diego, CA, USA) was used to prepare cDNA libraries. ENA-FIRST-PUBLIC 2017-12-18T17:02:51Z ENA-LAST-UPDATE 2017-04-19T13:22:23Z External Id SAMEA103983218 INSDC center name Freie Universitat Berlin Institut fur Biologie-Mikrobiologie INSDC first public 2017-12-18T17:02:51Z INSDC last update 2017-04-19T13:22:23Z INSDC status public Submitter Id E-MTAB-5666:Staph_aureus_NaOCl_III broker name ArrayExpress sample name E-MTAB-5666:Staph_aureus_NaOCl_III scientific_name Staphylococcus aureus subsp. aureus USA300