SRX12740008 GSM5651253 SRP342720 SRS10688252 GSM5651253 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from the spleens of mice vaccinated ID with LVS or one of the SCHU S4 deletion mutants ΔclpB, ΔgplX and ΔlpcC, (4 spleens from each group treated individually throughout) using Tri reagent (Life Technologies). Genomic DNA contamination was removed by Turbo DNA-Free Kit (Life Technologies). RNA was processed for paired-end RNA sequencing using Illumina Hi-Seq2000 (Genome Quebec). RNA-Seq Libraries were generated using the TruSeq strand RNA kit (Illumina). The RNA-Seq libraries were quantified by Qbit and qPCR according to the Illumina Sequencing Library qPCR Quantification Guide and the quality of the libraries was evaluated on Agilent Bioanalyzer 2100 using the Agilent DNA-100 chip. Illumina HiSeq 2000 gds 305651253 GSM5651253 GEO Accession GSM5651253 SRX12740009 GSM5651254 SRP342720 SRS10688253 GSM5651254 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from the spleens of mice vaccinated ID with LVS or one of the SCHU S4 deletion mutants ΔclpB, ΔgplX and ΔlpcC, (4 spleens from each group treated individually throughout) using Tri reagent (Life Technologies). Genomic DNA contamination was removed by Turbo DNA-Free Kit (Life Technologies). RNA was processed for paired-end RNA sequencing using Illumina Hi-Seq2000 (Genome Quebec). RNA-Seq Libraries were generated using the TruSeq strand RNA kit (Illumina). The RNA-Seq libraries were quantified by Qbit and qPCR according to the Illumina Sequencing Library qPCR Quantification Guide and the quality of the libraries was evaluated on Agilent Bioanalyzer 2100 using the Agilent DNA-100 chip. Illumina HiSeq 2000 gds 305651254 GSM5651254 GEO Accession GSM5651254 SRX12740010 GSM5651255 SRP342720 SRS10688254 GSM5651255 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from the spleens of mice vaccinated ID with LVS or one of the SCHU S4 deletion mutants ΔclpB, ΔgplX and ΔlpcC, (4 spleens from each group treated individually throughout) using Tri reagent (Life Technologies). Genomic DNA contamination was removed by Turbo DNA-Free Kit (Life Technologies). RNA was processed for paired-end RNA sequencing using Illumina Hi-Seq2000 (Genome Quebec). RNA-Seq Libraries were generated using the TruSeq strand RNA kit (Illumina). The RNA-Seq libraries were quantified by Qbit and qPCR according to the Illumina Sequencing Library qPCR Quantification Guide and the quality of the libraries was evaluated on Agilent Bioanalyzer 2100 using the Agilent DNA-100 chip. Illumina HiSeq 2000 gds 305651255 GSM5651255 GEO Accession GSM5651255 SRX12740011 GSM5651256 SRP342720 SRS10688255 GSM5651256 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from the spleens of mice vaccinated ID with LVS or one of the SCHU S4 deletion mutants ΔclpB, ΔgplX and ΔlpcC, (4 spleens from each group treated individually throughout) using Tri reagent (Life Technologies). Genomic DNA contamination was removed by Turbo DNA-Free Kit (Life Technologies). RNA was processed for paired-end RNA sequencing using Illumina Hi-Seq2000 (Genome Quebec). RNA-Seq Libraries were generated using the TruSeq strand RNA kit (Illumina). The RNA-Seq libraries were quantified by Qbit and qPCR according to the Illumina Sequencing Library qPCR Quantification Guide and the quality of the libraries was evaluated on Agilent Bioanalyzer 2100 using the Agilent DNA-100 chip. Illumina HiSeq 2000 gds 305651256 GSM5651256 GEO Accession GSM5651256 SRX12740012 GSM5651257 SRP342720 SRS10688256 GSM5651257 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from the spleens of mice vaccinated ID with LVS or one of the SCHU S4 deletion mutants ΔclpB, ΔgplX and ΔlpcC, (4 spleens from each group treated individually throughout) using Tri reagent (Life Technologies). Genomic DNA contamination was removed by Turbo DNA-Free Kit (Life Technologies). RNA was processed for paired-end RNA sequencing using Illumina Hi-Seq2000 (Genome Quebec). RNA-Seq Libraries were generated using the TruSeq strand RNA kit (Illumina). The RNA-Seq libraries were quantified by Qbit and qPCR according to the Illumina Sequencing Library qPCR Quantification Guide and the quality of the libraries was evaluated on Agilent Bioanalyzer 2100 using the Agilent DNA-100 chip. Illumina HiSeq 2000 gds 305651257 GSM5651257 GEO Accession GSM5651257 SRX12740013 GSM5651258 SRP342720 SRS10688257 GSM5651258 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from the spleens of mice vaccinated ID with LVS or one of the SCHU S4 deletion mutants ΔclpB, ΔgplX and ΔlpcC, (4 spleens from each group treated individually throughout) using Tri reagent (Life Technologies). Genomic DNA contamination was removed by Turbo DNA-Free Kit (Life Technologies). RNA was processed for paired-end RNA sequencing using Illumina Hi-Seq2000 (Genome Quebec). RNA-Seq Libraries were generated using the TruSeq strand RNA kit (Illumina). The RNA-Seq libraries were quantified by Qbit and qPCR according to the Illumina Sequencing Library qPCR Quantification Guide and the quality of the libraries was evaluated on Agilent Bioanalyzer 2100 using the Agilent DNA-100 chip. Illumina HiSeq 2000 gds 305651258 GSM5651258 GEO Accession GSM5651258 SRX12740014 GSM5651259 SRP342720 SRS10688258 GSM5651259 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from the spleens of mice vaccinated ID with LVS or one of the SCHU S4 deletion mutants ΔclpB, ΔgplX and ΔlpcC, (4 spleens from each group treated individually throughout) using Tri reagent (Life Technologies). Genomic DNA contamination was removed by Turbo DNA-Free Kit (Life Technologies). RNA was processed for paired-end RNA sequencing using Illumina Hi-Seq2000 (Genome Quebec). RNA-Seq Libraries were generated using the TruSeq strand RNA kit (Illumina). The RNA-Seq libraries were quantified by Qbit and qPCR according to the Illumina Sequencing Library qPCR Quantification Guide and the quality of the libraries was evaluated on Agilent Bioanalyzer 2100 using the Agilent DNA-100 chip. Illumina HiSeq 2000 gds 305651259 GSM5651259 GEO Accession GSM5651259 SRX12740015 GSM5651260 SRP342720 SRS10688259 GSM5651260 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from the spleens of mice vaccinated ID with LVS or one of the SCHU S4 deletion mutants ΔclpB, ΔgplX and ΔlpcC, (4 spleens from each group treated individually throughout) using Tri reagent (Life Technologies). Genomic DNA contamination was removed by Turbo DNA-Free Kit (Life Technologies). RNA was processed for paired-end RNA sequencing using Illumina Hi-Seq2000 (Genome Quebec). RNA-Seq Libraries were generated using the TruSeq strand RNA kit (Illumina). The RNA-Seq libraries were quantified by Qbit and qPCR according to the Illumina Sequencing Library qPCR Quantification Guide and the quality of the libraries was evaluated on Agilent Bioanalyzer 2100 using the Agilent DNA-100 chip. Illumina HiSeq 2000 gds 305651260 GSM5651260 GEO Accession GSM5651260 SRX12740016 GSM5651261 SRP342720 SRS10688260 GSM5651261 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from the spleens of mice vaccinated ID with LVS or one of the SCHU S4 deletion mutants ΔclpB, ΔgplX and ΔlpcC, (4 spleens from each group treated individually throughout) using Tri reagent (Life Technologies). Genomic DNA contamination was removed by Turbo DNA-Free Kit (Life Technologies). RNA was processed for paired-end RNA sequencing using Illumina Hi-Seq2000 (Genome Quebec). RNA-Seq Libraries were generated using the TruSeq strand RNA kit (Illumina). The RNA-Seq libraries were quantified by Qbit and qPCR according to the Illumina Sequencing Library qPCR Quantification Guide and the quality of the libraries was evaluated on Agilent Bioanalyzer 2100 using the Agilent DNA-100 chip. Illumina HiSeq 2000 gds 305651261 GSM5651261 GEO Accession GSM5651261 SRX12740017 GSM5651262 SRP342720 SRS10688261 GSM5651262 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from the spleens of mice vaccinated ID with LVS or one of the SCHU S4 deletion mutants ΔclpB, ΔgplX and ΔlpcC, (4 spleens from each group treated individually throughout) using Tri reagent (Life Technologies). Genomic DNA contamination was removed by Turbo DNA-Free Kit (Life Technologies). RNA was processed for paired-end RNA sequencing using Illumina Hi-Seq2000 (Genome Quebec). RNA-Seq Libraries were generated using the TruSeq strand RNA kit (Illumina). The RNA-Seq libraries were quantified by Qbit and qPCR according to the Illumina Sequencing Library qPCR Quantification Guide and the quality of the libraries was evaluated on Agilent Bioanalyzer 2100 using the Agilent DNA-100 chip. Illumina HiSeq 2000 gds 305651262 GSM5651262 GEO Accession GSM5651262 SRX12740018 GSM5651263 SRP342720 SRS10688262 GSM5651263 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from the spleens of mice vaccinated ID with LVS or one of the SCHU S4 deletion mutants ΔclpB, ΔgplX and ΔlpcC, (4 spleens from each group treated individually throughout) using Tri reagent (Life Technologies). Genomic DNA contamination was removed by Turbo DNA-Free Kit (Life Technologies). RNA was processed for paired-end RNA sequencing using Illumina Hi-Seq2000 (Genome Quebec). RNA-Seq Libraries were generated using the TruSeq strand RNA kit (Illumina). The RNA-Seq libraries were quantified by Qbit and qPCR according to the Illumina Sequencing Library qPCR Quantification Guide and the quality of the libraries was evaluated on Agilent Bioanalyzer 2100 using the Agilent DNA-100 chip. Illumina HiSeq 2000 gds 305651263 GSM5651263 GEO Accession GSM5651263 SRX12740019 GSM5651264 SRP342720 SRS10688263 GSM5651264 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from the spleens of mice vaccinated ID with LVS or one of the SCHU S4 deletion mutants ΔclpB, ΔgplX and ΔlpcC, (4 spleens from each group treated individually throughout) using Tri reagent (Life Technologies). Genomic DNA contamination was removed by Turbo DNA-Free Kit (Life Technologies). RNA was processed for paired-end RNA sequencing using Illumina Hi-Seq2000 (Genome Quebec). RNA-Seq Libraries were generated using the TruSeq strand RNA kit (Illumina). The RNA-Seq libraries were quantified by Qbit and qPCR according to the Illumina Sequencing Library qPCR Quantification Guide and the quality of the libraries was evaluated on Agilent Bioanalyzer 2100 using the Agilent DNA-100 chip. Illumina HiSeq 2000 gds 305651264 GSM5651264 GEO Accession GSM5651264 SRX12740020 GSM5651265 SRP342720 SRS10688264 GSM5651265 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from the spleens of mice vaccinated ID with LVS or one of the SCHU S4 deletion mutants ΔclpB, ΔgplX and ΔlpcC, (4 spleens from each group treated individually throughout) using Tri reagent (Life Technologies). Genomic DNA contamination was removed by Turbo DNA-Free Kit (Life Technologies). RNA was processed for paired-end RNA sequencing using Illumina Hi-Seq2000 (Genome Quebec). RNA-Seq Libraries were generated using the TruSeq strand RNA kit (Illumina). The RNA-Seq libraries were quantified by Qbit and qPCR according to the Illumina Sequencing Library qPCR Quantification Guide and the quality of the libraries was evaluated on Agilent Bioanalyzer 2100 using the Agilent DNA-100 chip. Illumina HiSeq 2000 gds 305651265 GSM5651265 GEO Accession GSM5651265 SRX12740021 GSM5651266 SRP342720 SRS10688265 GSM5651266 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from the spleens of mice vaccinated ID with LVS or one of the SCHU S4 deletion mutants ΔclpB, ΔgplX and ΔlpcC, (4 spleens from each group treated individually throughout) using Tri reagent (Life Technologies). Genomic DNA contamination was removed by Turbo DNA-Free Kit (Life Technologies). RNA was processed for paired-end RNA sequencing using Illumina Hi-Seq2000 (Genome Quebec). RNA-Seq Libraries were generated using the TruSeq strand RNA kit (Illumina). The RNA-Seq libraries were quantified by Qbit and qPCR according to the Illumina Sequencing Library qPCR Quantification Guide and the quality of the libraries was evaluated on Agilent Bioanalyzer 2100 using the Agilent DNA-100 chip. Illumina HiSeq 2000 gds 305651266 GSM5651266 GEO Accession GSM5651266 SRX12740022 GSM5651267 SRP342720 SRS10688266 GSM5651267 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from the spleens of mice vaccinated ID with LVS or one of the SCHU S4 deletion mutants ΔclpB, ΔgplX and ΔlpcC, (4 spleens from each group treated individually throughout) using Tri reagent (Life Technologies). Genomic DNA contamination was removed by Turbo DNA-Free Kit (Life Technologies). RNA was processed for paired-end RNA sequencing using Illumina Hi-Seq2000 (Genome Quebec). RNA-Seq Libraries were generated using the TruSeq strand RNA kit (Illumina). The RNA-Seq libraries were quantified by Qbit and qPCR according to the Illumina Sequencing Library qPCR Quantification Guide and the quality of the libraries was evaluated on Agilent Bioanalyzer 2100 using the Agilent DNA-100 chip. Illumina HiSeq 2000 gds 305651267 GSM5651267 GEO Accession GSM5651267 SRX12740023 GSM5651268 SRP342720 SRS10688267 GSM5651268 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from the spleens of mice vaccinated ID with LVS or one of the SCHU S4 deletion mutants ΔclpB, ΔgplX and ΔlpcC, (4 spleens from each group treated individually throughout) using Tri reagent (Life Technologies). Genomic DNA contamination was removed by Turbo DNA-Free Kit (Life Technologies). RNA was processed for paired-end RNA sequencing using Illumina Hi-Seq2000 (Genome Quebec). RNA-Seq Libraries were generated using the TruSeq strand RNA kit (Illumina). The RNA-Seq libraries were quantified by Qbit and qPCR according to the Illumina Sequencing Library qPCR Quantification Guide and the quality of the libraries was evaluated on Agilent Bioanalyzer 2100 using the Agilent DNA-100 chip. Illumina HiSeq 2000 gds 305651268 GSM5651268 GEO Accession GSM5651268 SRX12740024 GSM5651269 SRP342720 SRS10688268 GSM5651269 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from the spleens of mice vaccinated ID with LVS or one of the SCHU S4 deletion mutants ΔclpB, ΔgplX and ΔlpcC, (4 spleens from each group treated individually throughout) using Tri reagent (Life Technologies). Genomic DNA contamination was removed by Turbo DNA-Free Kit (Life Technologies). RNA was processed for paired-end RNA sequencing using Illumina Hi-Seq2000 (Genome Quebec). RNA-Seq Libraries were generated using the TruSeq strand RNA kit (Illumina). The RNA-Seq libraries were quantified by Qbit and qPCR according to the Illumina Sequencing Library qPCR Quantification Guide and the quality of the libraries was evaluated on Agilent Bioanalyzer 2100 using the Agilent DNA-100 chip. Illumina HiSeq 2000 gds 305651269 GSM5651269 GEO Accession GSM5651269 SRX12740025 GSM5651270 SRP342720 SRS10688269 GSM5651270 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from the spleens of mice vaccinated ID with LVS or one of the SCHU S4 deletion mutants ΔclpB, ΔgplX and ΔlpcC, (4 spleens from each group treated individually throughout) using Tri reagent (Life Technologies). Genomic DNA contamination was removed by Turbo DNA-Free Kit (Life Technologies). RNA was processed for paired-end RNA sequencing using Illumina Hi-Seq2000 (Genome Quebec). RNA-Seq Libraries were generated using the TruSeq strand RNA kit (Illumina). The RNA-Seq libraries were quantified by Qbit and qPCR according to the Illumina Sequencing Library qPCR Quantification Guide and the quality of the libraries was evaluated on Agilent Bioanalyzer 2100 using the Agilent DNA-100 chip. Illumina HiSeq 2000 gds 305651270 GSM5651270 GEO Accession GSM5651270 SRX12740026 GSM5651271 SRP342720 SRS10688270 GSM5651271 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from the spleens of mice vaccinated ID with LVS or one of the SCHU S4 deletion mutants ΔclpB, ΔgplX and ΔlpcC, (4 spleens from each group treated individually throughout) using Tri reagent (Life Technologies). Genomic DNA contamination was removed by Turbo DNA-Free Kit (Life Technologies). RNA was processed for paired-end RNA sequencing using Illumina Hi-Seq2000 (Genome Quebec). RNA-Seq Libraries were generated using the TruSeq strand RNA kit (Illumina). The RNA-Seq libraries were quantified by Qbit and qPCR according to the Illumina Sequencing Library qPCR Quantification Guide and the quality of the libraries was evaluated on Agilent Bioanalyzer 2100 using the Agilent DNA-100 chip. Illumina HiSeq 2000 gds 305651271 GSM5651271 GEO Accession GSM5651271 SRX12740027 GSM5651272 SRP342720 SRS10688271 GSM5651272 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from the spleens of mice vaccinated ID with LVS or one of the SCHU S4 deletion mutants ΔclpB, ΔgplX and ΔlpcC, (4 spleens from each group treated individually throughout) using Tri reagent (Life Technologies). Genomic DNA contamination was removed by Turbo DNA-Free Kit (Life Technologies). RNA was processed for paired-end RNA sequencing using Illumina Hi-Seq2000 (Genome Quebec). RNA-Seq Libraries were generated using the TruSeq strand RNA kit (Illumina). The RNA-Seq libraries were quantified by Qbit and qPCR according to the Illumina Sequencing Library qPCR Quantification Guide and the quality of the libraries was evaluated on Agilent Bioanalyzer 2100 using the Agilent DNA-100 chip. Illumina HiSeq 2000 gds 305651272 GSM5651272 GEO Accession GSM5651272