<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="GEO" alias="GSE216042" accession="SRP403278">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP403278</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA891752</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSE216042</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>Gene expression in Drosophila melanogaster in response to bacterial infection</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Transcriptome Analysis"/>
      <STUDY_ABSTRACT>The goal of this study was to generate a high-quality dataset of gene expression in Drosophila melanogaster 3 hours after infection with Gram-positive (M luteus) or Gram-negative (E coli) bacteria. Overall design: RNAseq on polyA-selected RNA extracted from whole male adult flies either uninjected or 3 hours after injection with 50nl of either: PBS (vehicle control), E coli suspended in PBS (OD600=1), M luteus suspended in PBS (OD600=1). Flies were kept at 29° after injection on our standard lab diet (10% yeast, 8% fructose, 2% polenta, 0.8% agar, supplemented with nipagin and propionic acid).</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>GSE216042</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
  </STUDY>
</STUDY_SET>
