<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX5263466" alias="PK_SW_500S10_3_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263466</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_500S10_3_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_500RPMS10_3_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264271">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264271</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_500S10_3_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_500S10_3_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263467" alias="PK_SW_500S10_3_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263467</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_500S10_3_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_500RPMS10_3_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264272">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264272</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_500S10_3_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_500S10_3_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263468" alias="PK_SW_100S8_2_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263468</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_100S8_2_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_100RPMS8_2_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264273">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264273</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_100S8_2_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_100S8_2_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263469" alias="PK_SW_100S8_2_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263469</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_100S8_2_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_100RPMS8_2_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264274">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264274</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_100S8_2_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_100S8_2_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263470" alias="PK_SW_100S8_3_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263470</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_100S8_3_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_100RPMS8_3_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264275">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264275</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_100S8_3_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_100S8_3_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263471" alias="PK_SW_100S8_3_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263471</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_100S8_3_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_100RPMS8_3_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264276">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264276</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_100S8_3_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_100S8_3_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263472" alias="PK_SW_500S10_1_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263472</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_500S10_1_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_500RPMS10_1_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264277">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264277</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_500S10_1_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_500S10_1_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263473" alias="PK_SW_500S10_1_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263473</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_500S10_1_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_500RPMS10_1_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264278">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264278</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_500S10_1_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_500S10_1_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263474" alias="PK_SW_500S10_2_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263474</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_500S10_2_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_500RPMS10_2_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264279">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264279</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_500S10_2_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_500S10_2_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263475" alias="PK_SW_500S10_2_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263475</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_500S10_2_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_500RPMS10_2_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264280">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264280</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_500S10_2_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_500S10_2_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263476" alias="PK_SW_FILTER_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263476</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_FILTER_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_FILTER_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264281">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264281</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_FILTER_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_FILTER_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263477" alias="PK_SW_FILTER_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263477</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_FILTER_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_FILTER_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264282">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264282</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_FILTER_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_FILTER_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263478" alias="PK_SW_500S8_2_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263478</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_500S8_2_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_500RPMS8_2_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264283">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264283</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_500S8_2_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_500S8_2_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263479" alias="PK_SW_500S8_2_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263479</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_500S8_2_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_500RPMS8_2_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264284">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264284</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_500S8_2_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_500S8_2_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263480" alias="PK_SW_500S8_3_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263480</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_500S8_3_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_500RPMS8_3_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264285">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264285</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_500S8_3_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_500S8_3_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263481" alias="PK_SW_500S8_3_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263481</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_500S8_3_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_500RPMS8_3_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264286">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264286</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_500S8_3_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_500S8_3_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263482" alias="PK_MC_500S2_2_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263482</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_MC_500S2_2_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_MC_500RPMS2_2_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264287">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264287</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_MC_500S2_2_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_MC_500S2_2_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263483" alias="PK_MC_500S2_2_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263483</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_MC_500S2_2_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_MC_500RPMS2_2_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264288">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264288</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_MC_500S2_2_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_MC_500S2_2_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263484" alias="PK_MC_500S10_2_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263484</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_MC_500S10_2_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_MC_500RPMS10_2_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264289">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264289</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_MC_500S10_2_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_MC_500S10_2_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263485" alias="PK_MC_500S10_2_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263485</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_MC_500S10_2_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_MC_500RPMS10_2_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264290">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264290</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_MC_500S10_2_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_MC_500S10_2_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263486" alias="PK_MC_500S2_1_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263486</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_MC_500S2_1_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_MC_500RPMS2_1_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264291">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264291</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_MC_500S2_1_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_MC_500S2_1_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263487" alias="PK_MC_500S2_1_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263487</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_MC_500S2_1_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_MC_500RPMS2_1_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264292">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264292</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_MC_500S2_1_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_MC_500S2_1_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263488" alias="PK_MC_100S6_2_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263488</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_MC_100S6_2_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_MC_100RPMS6_2_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264293">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264293</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_MC_100S6_2_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_MC_100S6_2_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263489" alias="PK_MC_100S6_2_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263489</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_MC_100S6_2_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_MC_100RPMS6_2_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264294">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264294</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_MC_100S6_2_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_MC_100S6_2_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263490" alias="PK_MC_500S10_1_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263490</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_MC_500S10_1_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_MC_500RPMS10_1_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264295">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264295</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_MC_500S10_1_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_MC_500S10_1_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263491" alias="PK_MC_500S10_1_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263491</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_MC_500S10_1_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_MC_500RPMS10_1_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264296">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264296</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_MC_500S10_1_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_MC_500S10_1_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263492" alias="PK_SW_500S6_3_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263492</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_500S6_3_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_500RPMS6_3_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264297">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264297</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_500S6_3_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_500S6_3_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263493" alias="PK_SW_500S6_3_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263493</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_500S6_3_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_500RPMS6_3_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264298">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264298</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_500S6_3_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_500S6_3_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263494" alias="PK_SW_500S6_2_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263494</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_500S6_2_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_500RPMS6_2_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264299">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264299</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_500S6_2_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_500S6_2_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263495" alias="PK_SW_500S6_2_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263495</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_500S6_2_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_500RPMS6_2_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264300">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264300</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_500S6_2_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_500S6_2_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263496" alias="PK_SW_500S6_1_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263496</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_500S6_1_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_500RPMS6_1_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264301">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264301</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_500S6_1_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_500S6_1_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263497" alias="PK_SW_500S6_1_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263497</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_500S6_1_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_500RPMS6_1_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264302">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264302</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_500S6_1_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_500S6_1_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263498" alias="PK_SW_500S4_3_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263498</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_500S4_3_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_500RPMS4_3_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264303">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264303</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_500S4_3_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_500S4_3_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263499" alias="PK_SW_500S4_3_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263499</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_500S4_3_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_500RPMS4_3_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264304">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264304</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_500S4_3_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_500S4_3_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263500" alias="PK_SW_500S8_1_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263500</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_500S8_1_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_500RPMS8_1_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264305">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264305</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_500S8_1_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_500S8_1_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263501" alias="PK_SW_500S8_1_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263501</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_500S8_1_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_500RPMS8_1_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264306">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264306</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_500S8_1_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_500S8_1_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263502" alias="PK_SW_100S10_3_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263502</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_100S10_3_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_100RPMS10_3_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264307">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264307</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_100S10_3_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_100S10_3_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263503" alias="PK_SW_100S10_3_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263503</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_100S10_3_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_100RPMS10_3_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264308">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264308</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_100S10_3_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_100S10_3_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263504" alias="PK_MC_FILTER_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263504</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_MC_FILTER_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_MC_FILTER_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264309">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264309</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_MC_FILTER_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_MC_FILTER_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263505" alias="PK_MC_FILTER_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263505</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_MC_FILTER_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_MC_FILTER_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264310">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264310</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_MC_FILTER_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_MC_FILTER_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263506" alias="PK_MC_500S8_2_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263506</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_MC_500S8_2_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_MC_500RPMS8_2_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264311">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264311</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_MC_500S8_2_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_MC_500S8_2_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263507" alias="PK_MC_500S8_2_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263507</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_MC_500S8_2_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_MC_500RPMS8_2_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264312">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264312</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_MC_500S8_2_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_MC_500S8_2_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263508" alias="PK_SW_100S10_2_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263508</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_100S10_2_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_100RPMS10_2_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264313">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264313</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_100S10_2_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_100S10_2_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263509" alias="PK_SW_100S10_2_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263509</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_100S10_2_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_100RPMS10_2_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264314">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264314</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_100S10_2_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_100S10_2_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263510" alias="PK_SW_100S10_1_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263510</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_100S10_1_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_100RPMS10_1_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264315">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264315</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_100S10_1_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_100S10_1_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263511" alias="PK_SW_100S10_1_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263511</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_100S10_1_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_100RPMS10_1_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264316">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264316</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_100S10_1_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_100S10_1_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263512" alias="PK_MC_500S6_1_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263512</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_MC_500S6_1_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_MC_500RPMS6_1_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264317">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264317</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_MC_500S6_1_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_MC_500S6_1_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263513" alias="PK_MC_500S6_1_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263513</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_MC_500S6_1_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_MC_500RPMS6_1_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264318">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264318</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_MC_500S6_1_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_MC_500S6_1_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263514" alias="PK_MC_500S6_2_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263514</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_MC_500S6_2_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_MC_500RPMS6_2_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264319">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264319</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_MC_500S6_2_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_MC_500S6_2_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263515" alias="PK_MC_500S6_2_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263515</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_MC_500S6_2_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_MC_500RPMS6_2_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264320">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264320</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_MC_500S6_2_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_MC_500S6_2_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263516" alias="PK_MC_500S4_1_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263516</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_MC_500S4_1_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_MC_500RPMS4_1_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264321">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264321</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_MC_500S4_1_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_MC_500S4_1_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263517" alias="PK_MC_500S4_1_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263517</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_MC_500S4_1_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_MC_500RPMS4_1_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264322">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264322</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_MC_500S4_1_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_MC_500S4_1_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263518" alias="PK_MC_500S4_2_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263518</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_MC_500S4_2_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_MC_500RPMS4_2_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264323">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264323</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_MC_500S4_2_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_MC_500S4_2_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263519" alias="PK_MC_500S4_2_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263519</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_MC_500S4_2_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_MC_500RPMS4_2_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264324">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264324</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_MC_500S4_2_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_MC_500S4_2_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263520" alias="PK_MC_500S8_1_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263520</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_MC_500S8_1_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_MC_500RPMS8_1_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264325">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264325</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_MC_500S8_1_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_MC_500S8_1_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263521" alias="PK_MC_500S8_1_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263521</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_MC_500S8_1_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_MC_500RPMS8_1_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264326">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264326</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_MC_500S8_1_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_MC_500S8_1_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263522" alias="PK_SW_100S4_3_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263522</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_100S4_3_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_100RPMS4_3_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264327">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264327</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_100S4_3_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_100S4_3_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263523" alias="PK_SW_100S4_3_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263523</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_100S4_3_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_100RPMS4_3_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264328">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264328</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_100S4_3_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_100S4_3_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263524" alias="PK_SW_100S6_1_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263524</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_100S6_1_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_100RPMS6_1_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264329">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264329</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_100S6_1_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_100S6_1_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263525" alias="PK_SW_100S6_1_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263525</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_100S6_1_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_100RPMS6_1_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264330">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264330</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_100S6_1_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_100S6_1_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263526" alias="PK_SW_100S6_2_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263526</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_100S6_2_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_100RPMS6_2_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264331">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264331</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_100S6_2_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_100S6_2_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263527" alias="PK_SW_100S6_2_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263527</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_100S6_2_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_100RPMS6_2_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264332">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264332</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_100S6_2_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_100S6_2_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263528" alias="PK_SW_100S6_3_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263528</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_100S6_3_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_100RPMS6_3_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264333">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264333</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_100S6_3_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_100S6_3_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263529" alias="PK_SW_100S6_3_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263529</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_100S6_3_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_100RPMS6_3_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264334">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264334</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_100S6_3_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_100S6_3_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263530" alias="PK_SW_100S8_1_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263530</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_100S8_1_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_100RPMS8_1_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264335">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264335</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_100S8_1_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_100S8_1_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263531" alias="PK_SW_100S8_1_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263531</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_100S8_1_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_100RPMS8_1_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264336">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264336</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_100S8_1_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_100S8_1_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263532" alias="PK_MC_100S6_1_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263532</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_MC_100S6_1_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_MC_100RPMS6_1_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264337">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264337</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_MC_100S6_1_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_MC_100S6_1_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263533" alias="PK_MC_100S6_1_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263533</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_MC_100S6_1_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_MC_100RPMS6_1_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264338">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264338</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_MC_100S6_1_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_MC_100S6_1_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263534" alias="PK_MC_100S4_1_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263534</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_MC_100S4_1_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_MC_100RPMS4_1_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264339">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264339</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_MC_100S4_1_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_MC_100S4_1_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263535" alias="PK_MC_100S4_1_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263535</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_MC_100S4_1_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_MC_100RPMS4_1_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264340">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264340</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_MC_100S4_1_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_MC_100S4_1_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263536" alias="PK_MC_100S4_2_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263536</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_MC_100S4_2_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_MC_100RPMS4_2_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264341">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264341</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_MC_100S4_2_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_MC_100S4_2_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263537" alias="PK_MC_100S4_2_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263537</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_MC_100S4_2_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_MC_100RPMS4_2_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264342">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264342</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_MC_100S4_2_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_MC_100S4_2_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263538" alias="PK_MC_100S2_1_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263538</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_MC_100S2_1_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_MC_100RPMS2_1_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264343">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264343</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_MC_100S2_1_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_MC_100S2_1_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263539" alias="PK_MC_100S2_1_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263539</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_MC_100S2_1_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_MC_100RPMS2_1_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264344">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264344</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_MC_100S2_1_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_MC_100S2_1_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263540" alias="PK_MC_100S2_2_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263540</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_MC_100S2_2_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_MC_100RPMS2_2_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264345">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264345</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_MC_100S2_2_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_MC_100S2_2_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263541" alias="PK_MC_100S2_2_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263541</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_MC_100S2_2_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_MC_100RPMS2_2_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264346">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264346</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_MC_100S2_2_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_MC_100S2_2_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263542" alias="PK_SW_100S2_2_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263542</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_100S2_2_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_100RPMS2_2_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264347">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264347</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_100S2_2_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_100S2_2_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263543" alias="PK_SW_100S2_2_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263543</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_100S2_2_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_100RPMS2_2_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264348">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264348</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_100S2_2_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_100S2_2_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263544" alias="PK_SW_100S2_1_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263544</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_100S2_1_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_100RPMS2_1_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264349">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264349</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_100S2_1_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_100S2_1_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263545" alias="PK_SW_100S2_1_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263545</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_100S2_1_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_100RPMS2_1_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264350">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264350</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_100S2_1_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_100S2_1_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263546" alias="PK_SW_100S4_1_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263546</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_100S4_1_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_100RPMS4_1_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264351">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264351</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_100S4_1_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_100S4_1_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263547" alias="PK_SW_100S4_1_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263547</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_100S4_1_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_100RPMS4_1_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264352">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264352</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_100S4_1_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_100S4_1_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263548" alias="PK_SW_100S2_3_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263548</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_100S2_3_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_100RPMS2_3_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264353">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264353</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_100S2_3_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_100S2_3_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263549" alias="PK_SW_100S2_3_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263549</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_100S2_3_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_100RPMS2_3_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264354">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264354</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_100S2_3_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_100S2_3_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263550" alias="PK_SW_100S4_2_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263550</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_100S4_2_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_100RPMS4_2_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264355">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264355</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_100S4_2_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_100S4_2_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263551" alias="PK_SW_100S4_2_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263551</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_100S4_2_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_100RPMS4_2_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264356">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264356</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_100S4_2_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_100S4_2_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263552" alias="PK_SW_500S4_2_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263552</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_500S4_2_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_500RPMS4_2_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264357">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264357</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_500S4_2_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_500S4_2_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263553" alias="PK_SW_500S4_2_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263553</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_500S4_2_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_500RPMS4_2_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264358">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264358</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_500S4_2_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_500S4_2_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263554" alias="PK_SW_500S4_1_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263554</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_500S4_1_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_500RPMS4_1_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264359">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264359</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_500S4_1_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_500S4_1_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263555" alias="PK_SW_500S4_1_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263555</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_500S4_1_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_500RPMS4_1_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264360">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264360</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_500S4_1_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_500S4_1_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263556" alias="PK_SW_500S2_3_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263556</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_500S2_3_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_500RPMS2_3_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264361">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264361</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_500S2_3_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_500S2_3_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263557" alias="PK_SW_500S2_3_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263557</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_500S2_3_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_500RPMS2_3_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264362">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264362</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_500S2_3_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_500S2_3_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263558" alias="PK_SW_500S2_2_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263558</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_500S2_2_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_500RPMS2_2_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264363">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264363</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_500S2_2_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_500S2_2_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263559" alias="PK_SW_500S2_2_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263559</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_500S2_2_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_500RPMS2_2_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264364">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264364</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_500S2_2_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_500S2_2_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263560" alias="PK_SW_500S2_1_T">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263560</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_500S2_1_T</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_500RPMS2_1_Transconjugant</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264365">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264365</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_500S2_1_T</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_500S2_1_T</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5263561" alias="PK_SW_500S2_1_R">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5263561</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5049811">PK_SW_500S2_1_R</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>pKJK5_SW_500RPMS2_1_Recipient</TITLE>
    <STUDY_REF accession="SRP180298">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP180298</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5049811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR of the 16S rRNA  V3-V4 were done using primer set 341F and 806R. Individual samples were then tagged using loci-specific indexing primers in a second PCR step, then purified using HighPrep PCR magnetic beads and pooled. Pooled libraries were then sequenced on a Illumina MiSeq platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4264366">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4264366</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|leeliguan@gmail.com">PK_SW_500S2_1_R</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>PK_SW_500S2_1_R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
