<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="GEO" alias="GSE123434" accession="SRP172735">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP172735</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA508744</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSE123434</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>Dual RNA-seq of Neisseria gonorrhoeae and human neutrophils</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Other"/>
      <STUDY_ABSTRACT>Deep sequencing of cDNA from Neisseria gonorrhoeae bacteria and human neutrophils, alone and after coincubation. Overall design: Total RNA was isolated from Neisseria gonorrhoeae and adherent primary human neutrophils, alone and after co-culture over time. Bacteria were of strain FA1090 ?opa ("Opaless"; 130), FA1090 ?opa with H041 penA, penB, and mtrR resistance alleles (3x130), or H041. Bacteria were untreated or treated with experimentally determined sublethal concentrations of selected antibiotics 1 hour prior to and during co-culture. Ribosomal RNA was depleted and the remaining RNA was reverse-transcribed into a cDNA library for Illumina sequencing. Reads were mapped to the FA1090, H041 and/or human genomes.</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>GSE123434</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
    <STUDY_LINKS>
      <STUDY_LINK>
        <XREF_LINK>
          <DB>pubmed</DB>
          <ID>37387581</ID>
        </XREF_LINK>
      </STUDY_LINK>
      <STUDY_LINK>
        <XREF_LINK>
          <DB>pubmed</DB>
          <ID>38976720</ID>
        </XREF_LINK>
      </STUDY_LINK>
    </STUDY_LINKS>
  </STUDY>
</STUDY_SET>
