<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX6921514" alias="LbPt-1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6921514</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6357079">LbPt-1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Lactobacillus plantarum Transcriptome Sequencing</TITLE>
    <STUDY_REF accession="SRP223653">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223653</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB6357079">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fragmentation of rRNA depleted mRNA samples and subsequent preparation of cDNA libraries were performed using Illumina TruSeq Stranded mRNA Library Preparation kit (Low Sample Protocol), following manufacturers instructions. First cDNA strand synthesis in the reverse transcription polymerase chain reaction (RT-PCR) was performed using the reagents supplied by the manufacturer along with the SuperScript II reverse transcriptase (Thermo Fisher Scientific).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5452632">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5452632</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12871320</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>LbPt-1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RT-PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6921515" alias="LbPt-2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6921515</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6357079">LbPt-2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Lactobacillus plantarum Transcriptome Sequencing</TITLE>
    <STUDY_REF accession="SRP223653">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223653</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB6357079">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fragmentation of rRNA depleted mRNA samples and subsequent preparation of cDNA libraries were performed using Illumina TruSeq Stranded mRNA Library Preparation kit (Low Sample Protocol), following manufacturers instructions. First cDNA strand synthesis in the reverse transcription polymerase chain reaction (RT-PCR) was performed using the reagents supplied by the manufacturer along with the SuperScript II reverse transcriptase (Thermo Fisher Scientific).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5452632">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5452632</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12871320</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>LbPt-2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RT-PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6921516" alias="LbSv-2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6921516</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6357079">LbSv-2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Lactobacillus salivarius Transcriptome Sequencing</TITLE>
    <STUDY_REF accession="SRP223653">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223653</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB6357079">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fragmentation of rRNA depleted mRNA samples and subsequent preparation of cDNA libraries were performed using Illumina TruSeq Stranded mRNA Library Preparation kit (Low Sample Protocol), following manufacturers instructions. First cDNA strand synthesis in the reverse transcription polymerase chain reaction (RT-PCR) was performed using the reagents supplied by the manufacturer along with the SuperScript II reverse transcriptase (Thermo Fisher Scientific).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5452633">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5452633</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12871356</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>LbSv-2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RT-PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6921517" alias="LbSv-3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6921517</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6357079">LbSv-3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Lactobacillus salivarius Transcriptome Sequencing</TITLE>
    <STUDY_REF accession="SRP223653">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223653</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB6357079">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fragmentation of rRNA depleted mRNA samples and subsequent preparation of cDNA libraries were performed using Illumina TruSeq Stranded mRNA Library Preparation kit (Low Sample Protocol), following manufacturers instructions. First cDNA strand synthesis in the reverse transcription polymerase chain reaction (RT-PCR) was performed using the reagents supplied by the manufacturer along with the SuperScript II reverse transcriptase (Thermo Fisher Scientific).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5452633">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5452633</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12871356</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>LbSv-3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RT-PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6921518" alias="LbFm-1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6921518</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6357079">LbFm-1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Lactobacillus fermentum Transcriptome Sequencing</TITLE>
    <STUDY_REF accession="SRP223653">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223653</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB6357079">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fragmentation of rRNA depleted mRNA samples and subsequent preparation of cDNA libraries were performed using Illumina TruSeq Stranded mRNA Library Preparation kit (Low Sample Protocol), following manufacturers instructions. First cDNA strand synthesis in the reverse transcription polymerase chain reaction (RT-PCR) was performed using the reagents supplied by the manufacturer along with the SuperScript II reverse transcriptase (Thermo Fisher Scientific).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5452634">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5452634</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12871372</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>LbFm-1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RT-PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6921519" alias="LbFm-2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6921519</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6357079">LbFm-2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Lactobacillus fermentum Transcriptome Sequencing</TITLE>
    <STUDY_REF accession="SRP223653">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223653</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB6357079">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fragmentation of rRNA depleted mRNA samples and subsequent preparation of cDNA libraries were performed using Illumina TruSeq Stranded mRNA Library Preparation kit (Low Sample Protocol), following manufacturers instructions. First cDNA strand synthesis in the reverse transcription polymerase chain reaction (RT-PCR) was performed using the reagents supplied by the manufacturer along with the SuperScript II reverse transcriptase (Thermo Fisher Scientific).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5452634">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5452634</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12871372</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>LbFm-2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RT-PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6921520" alias="LbFm-3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6921520</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6357079">LbFm-3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Lactobacillus fermentum Transcriptome Sequencing</TITLE>
    <STUDY_REF accession="SRP223653">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223653</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB6357079">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fragmentation of rRNA depleted mRNA samples and subsequent preparation of cDNA libraries were performed using Illumina TruSeq Stranded mRNA Library Preparation kit (Low Sample Protocol), following manufacturers instructions. First cDNA strand synthesis in the reverse transcription polymerase chain reaction (RT-PCR) was performed using the reagents supplied by the manufacturer along with the SuperScript II reverse transcriptase (Thermo Fisher Scientific).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5452634">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5452634</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12871372</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>LbFm-3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RT-PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6921521" alias="LeMt-1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6921521</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6357079">LeMt-1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Leuconostoc mesenteroides subsp. mesenteroides Transcriptome Sequencing</TITLE>
    <STUDY_REF accession="SRP223653">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223653</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB6357079">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fragmentation of rRNA depleted mRNA samples and subsequent preparation of cDNA libraries were performed using Illumina TruSeq Stranded mRNA Library Preparation kit (Low Sample Protocol), following manufacturers instructions. First cDNA strand synthesis in the reverse transcription polymerase chain reaction (RT-PCR) was performed using the reagents supplied by the manufacturer along with the SuperScript II reverse transcriptase (Thermo Fisher Scientific).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5452635">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5452635</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12871373</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>LeMt-1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RT-PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6921522" alias="LeMt-2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6921522</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6357079">LeMt-2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Leuconostoc mesenteroides subsp. mesenteroides Transcriptome Sequencing</TITLE>
    <STUDY_REF accession="SRP223653">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223653</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB6357079">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fragmentation of rRNA depleted mRNA samples and subsequent preparation of cDNA libraries were performed using Illumina TruSeq Stranded mRNA Library Preparation kit (Low Sample Protocol), following manufacturers instructions. First cDNA strand synthesis in the reverse transcription polymerase chain reaction (RT-PCR) was performed using the reagents supplied by the manufacturer along with the SuperScript II reverse transcriptase (Thermo Fisher Scientific).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5452635">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5452635</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12871373</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>LeMt-2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RT-PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6921523" alias="LeMt-3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6921523</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6357079">LeMt-3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Leuconostoc mesenteroides subsp. mesenteroides Transcriptome Sequencing</TITLE>
    <STUDY_REF accession="SRP223653">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223653</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB6357079">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fragmentation of rRNA depleted mRNA samples and subsequent preparation of cDNA libraries were performed using Illumina TruSeq Stranded mRNA Library Preparation kit (Low Sample Protocol), following manufacturers instructions. First cDNA strand synthesis in the reverse transcription polymerase chain reaction (RT-PCR) was performed using the reagents supplied by the manufacturer along with the SuperScript II reverse transcriptase (Thermo Fisher Scientific).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5452635">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5452635</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12871373</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>LeMt-3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RT-PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6921524" alias="LbPt-3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6921524</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6357079">LbPt-3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Lactobacillus plantarum Transcriptome Sequencing</TITLE>
    <STUDY_REF accession="SRP223653">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223653</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB6357079">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fragmentation of rRNA depleted mRNA samples and subsequent preparation of cDNA libraries were performed using Illumina TruSeq Stranded mRNA Library Preparation kit (Low Sample Protocol), following manufacturers instructions. First cDNA strand synthesis in the reverse transcription polymerase chain reaction (RT-PCR) was performed using the reagents supplied by the manufacturer along with the SuperScript II reverse transcriptase (Thermo Fisher Scientific).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5452632">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5452632</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12871320</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>LbPt-3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RT-PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6921525" alias="LcLt-1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6921525</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6357079">LcLt-1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Lactococcus lactis subsp. cremoris Transcriptome Sequencing</TITLE>
    <STUDY_REF accession="SRP223653">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223653</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB6357079">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fragmentation of rRNA depleted mRNA samples and subsequent preparation of cDNA libraries were performed using Illumina TruSeq Stranded mRNA Library Preparation kit (Low Sample Protocol), following manufacturers instructions. First cDNA strand synthesis in the reverse transcription polymerase chain reaction (RT-PCR) was performed using the reagents supplied by the manufacturer along with the SuperScript II reverse transcriptase (Thermo Fisher Scientific).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5452636">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5452636</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12871321</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>LcLt-1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RT-PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6921526" alias="LcLt-2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6921526</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6357079">LcLt-2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Lactococcus lactis subsp. cremoris Transcriptome Sequencing</TITLE>
    <STUDY_REF accession="SRP223653">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223653</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB6357079">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fragmentation of rRNA depleted mRNA samples and subsequent preparation of cDNA libraries were performed using Illumina TruSeq Stranded mRNA Library Preparation kit (Low Sample Protocol), following manufacturers instructions. First cDNA strand synthesis in the reverse transcription polymerase chain reaction (RT-PCR) was performed using the reagents supplied by the manufacturer along with the SuperScript II reverse transcriptase (Thermo Fisher Scientific).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5452636">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5452636</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12871321</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>LcLt-2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RT-PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6921527" alias="LcLt-3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6921527</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6357079">LcLt-3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Lactococcus lactis subsp. cremoris Transcriptome Sequencing</TITLE>
    <STUDY_REF accession="SRP223653">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223653</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB6357079">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fragmentation of rRNA depleted mRNA samples and subsequent preparation of cDNA libraries were performed using Illumina TruSeq Stranded mRNA Library Preparation kit (Low Sample Protocol), following manufacturers instructions. First cDNA strand synthesis in the reverse transcription polymerase chain reaction (RT-PCR) was performed using the reagents supplied by the manufacturer along with the SuperScript II reverse transcriptase (Thermo Fisher Scientific).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5452636">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5452636</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12871321</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>LcLt-3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RT-PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6921528" alias="LbCs-1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6921528</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6357079">LbCs-1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Lactobacillus casei subsp. casei Transcriptome Sequencing</TITLE>
    <STUDY_REF accession="SRP223653">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223653</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB6357079">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fragmentation of rRNA depleted mRNA samples and subsequent preparation of cDNA libraries were performed using Illumina TruSeq Stranded mRNA Library Preparation kit (Low Sample Protocol), following manufacturers instructions. First cDNA strand synthesis in the reverse transcription polymerase chain reaction (RT-PCR) was performed using the reagents supplied by the manufacturer along with the SuperScript II reverse transcriptase (Thermo Fisher Scientific).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5452637">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5452637</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12871331</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>LbCs-1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RT-PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6921529" alias="LbCs-2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6921529</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6357079">LbCs-2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Lactobacillus casei subsp. casei Transcriptome Sequencing</TITLE>
    <STUDY_REF accession="SRP223653">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223653</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB6357079">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fragmentation of rRNA depleted mRNA samples and subsequent preparation of cDNA libraries were performed using Illumina TruSeq Stranded mRNA Library Preparation kit (Low Sample Protocol), following manufacturers instructions. First cDNA strand synthesis in the reverse transcription polymerase chain reaction (RT-PCR) was performed using the reagents supplied by the manufacturer along with the SuperScript II reverse transcriptase (Thermo Fisher Scientific).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5452637">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5452637</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12871331</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>LbCs-2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RT-PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6921530" alias="LbCs-3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6921530</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6357079">LbCs-3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Lactobacillus casei subsp. casei Transcriptome Sequencing</TITLE>
    <STUDY_REF accession="SRP223653">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223653</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB6357079">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fragmentation of rRNA depleted mRNA samples and subsequent preparation of cDNA libraries were performed using Illumina TruSeq Stranded mRNA Library Preparation kit (Low Sample Protocol), following manufacturers instructions. First cDNA strand synthesis in the reverse transcription polymerase chain reaction (RT-PCR) was performed using the reagents supplied by the manufacturer along with the SuperScript II reverse transcriptase (Thermo Fisher Scientific).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5452637">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5452637</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12871331</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>LbCs-3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RT-PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6921531" alias="LbSv-1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6921531</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6357079">LbSv-1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Lactobacillus salivarius Transcriptome Sequencing</TITLE>
    <STUDY_REF accession="SRP223653">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223653</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB6357079">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fragmentation of rRNA depleted mRNA samples and subsequent preparation of cDNA libraries were performed using Illumina TruSeq Stranded mRNA Library Preparation kit (Low Sample Protocol), following manufacturers instructions. First cDNA strand synthesis in the reverse transcription polymerase chain reaction (RT-PCR) was performed using the reagents supplied by the manufacturer along with the SuperScript II reverse transcriptase (Thermo Fisher Scientific).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5452633">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5452633</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12871356</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>LbSv-1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RT-PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
