<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="BioProject" alias="PRJNA450709" accession="SRP142225">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP142225</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA450709</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>Metagenome-wide association analysis identifies microbial determinants of post-antibiotic ecological recovery in the gut</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Other"/>
      <STUDY_ABSTRACT>Loss of diversity in the gut microbiome can persist for extended periods of time after antibiotic treatment, impacting microbiome function, antimicrobial resistance and likely host health. Despite widespread antibiotic use, our understanding of species and metabolic functions contributing to gut microbiome recovery is limited. Using data from 4 different discovery cohorts in 3 continents comprising &gt;500 microbiome profiles from 117 subjects, we identified 21 bacterial species exhibiting robust association with ecological recovery post antibiotic therapy. Functional and growth-rate analysis showed that recovery is supported by enrichment in specific carbohydrate degradation and energy production pathways. Association rule mining on 782 microbiome profiles from the MEDUSA database enabled reconstruction of the gut microbial food-web, identifying many recovery-associated bacteria (RABs) as keystone species, with the ability to use host and diet-derived energy sources, and support the repopulation of other gut species. Experiments in a mouse model recapitulated the ability of RABs (Bacteroides thetaiotamicron and Bifidobacterium adolescentis) to promote recovery with synergistic effects, providing a two orders of magnitude boost to microbial abundance in early time-points and faster maturation of microbial diversity. The identification of specific species and metabolic functions promoting recovery opens up opportunities for rationally determining pre- and probiotic formulations that can protect us from long-term consequences of frequent antibiotic usage.</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>Mouse gut metagenome</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
  </STUDY>
</STUDY_SET>
