<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>7(11)</volume><submitter>Young BC</submitter><funding>department of health</funding><funding>Medical Research Council</funding><funding>wellcome trust</funding><funding>National Institute for Health Research (NIHR)</funding><funding>fondation mérieux</funding><funding>Wellcome Trust</funding><funding>nihr oxford biomedical research centre</funding><pubmed_abstract>&lt;i>Staphylococcus aureus&lt;/i> is a major bacterial pathogen in humans, and a dominant cause of severe bloodstream infections. Globally, antimicrobial resistance (AMR) in &lt;i>S. aureus&lt;/i> remains challenging. While human risk factors for infection have been defined, contradictory evidence exists for the role of bacterial genomic variation in &lt;i>S. aureus&lt;/i> disease. To investigate the contribution of bacterial lineage and genomic variation to the development of bloodstream infection, we undertook a genome-wide association study comparing bacteria from 1017 individuals with bacteraemia to 984 adults with asymptomatic &lt;i>S. aureus&lt;/i> nasal carriage. Within 984 carriage isolates, we also compared healthcare-associated (HA) carriage with community-associated (CA) carriage. All major global lin</pubmed_abstract><journal>Microbial genomics</journal><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8743558</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Antimicrobial resistance determinants are associated with &amp;lt;i&amp;gt;Staphylococcus aureus&amp;lt;/i&amp;gt; bacteraemia and adaptation to the healthcare environment: a bacterial genome-wide association study.</pubmed_title><pmcid>PMC8743558</pmcid><funding_grant_id>Grant 101611/Z/13/Z</funding_grant_id><funding_grant_id>Grant 101237/Z/13/B</funding_grant_id><funding_grant_id>MR/K023985/1</funding_grant_id><funding_grant_id>101237/Z/13/Z</funding_grant_id><funding_grant_id>HDR-9006</funding_grant_id><funding_grant_id>NF-SI-0508-10279</funding_grant_id><funding_grant_id>101611/Z/13/Z</funding_grant_id><funding_grant_id>NIHR200239</funding_grant_id><funding_grant_id>203141/Z/16/Z</funding_grant_id><funding_grant_id>grant HICF-T5-358</funding_grant_id><funding_grant_id>WT098615/Z/12/Z</funding_grant_id><funding_grant_id>CL-2017-13-009</funding_grant_id><funding_grant_id>101237/Z/13/B</funding_grant_id><funding_grant_id>HPRU-2012-10041</funding_grant_id><pubmed_authors>Peto TE</pubmed_authors><pubmed_authors>Godwin H</pubmed_authors><pubmed_authors>Quan TP</pubmed_authors><pubmed_authors>Wilson DJ</pubmed_authors><pubmed_authors>Tilley R</pubmed_authors><pubmed_authors>Llewelyn MJ</pubmed_authors><pubmed_authors>Charlesworth J</pubmed_authors><pubmed_authors>Scarborough M</pubmed_authors><pubmed_authors>Young BC</pubmed_authors><pubmed_authors>Gordon NC</pubmed_authors><pubmed_authors>Knox K</pubmed_authors><pubmed_authors>Oakley S</pubmed_authors><pubmed_authors>Price JR</pubmed_authors><pubmed_authors>Fung R</pubmed_authors><pubmed_authors>Miller R</pubmed_authors><pubmed_authors>Earle S</pubmed_authors><pubmed_authors>Dunn L</pubmed_authors><pubmed_authors>Walker AS</pubmed_authors><pubmed_authors>Cole K</pubmed_authors><pubmed_authors>Votintseva A</pubmed_authors><pubmed_authors>Wu CH</pubmed_authors><pubmed_authors>Crook DW</pubmed_authors><pubmed_authors>Liu E</pubmed_authors></additional><is_claimable>false</is_claimable><name>Antimicrobial resistance determinants are associated with &amp;lt;i&amp;gt;Staphylococcus aureus&amp;lt;/i&amp;gt; bacteraemia and adaptation to the healthcare environment: a bacterial genome-wide association study.</name><description>&lt;i>Staphylococcus aureus&lt;/i> is a major bacterial pathogen in humans, and a dominant cause of severe bloodstream infections. Globally, antimicrobial resistance (AMR) in &lt;i>S. aureus&lt;/i> remains challenging. While human risk factors for infection have been defined, contradictory evidence exists for the role of bacterial genomic variation in &lt;i>S. aureus&lt;/i> disease. To investigate the contribution of bacterial lineage and genomic variation to the development of bloodstream infection, we undertook a genome-wide association study comparing bacteria from 1017 individuals with bacteraemia to 984 adults with asymptomatic &lt;i>S. aureus&lt;/i> nasal carriage. Within 984 carriage isolates, we also compared healthcare-associated (HA) carriage with community-associated (CA) carriage. All major global lin</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Nov</publication><modification>2026-05-07T19:43:56.867Z</modification><creation>2022-02-11T15:07:47.566Z</creation></dates><accession>S-EPMC8743558</accession><cross_references><pubmed>34812717</pubmed><doi>10.1099/mgen.0.000700</doi></cross_references></HashMap>