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dc.contributor.authorGoswami, Cosmika
dc.contributor.authorFox, Stephen
dc.contributor.authorHolden, Matthew
dc.contributor.authorConnor, Martin
dc.contributor.authorLeanord, Alistair
dc.contributor.authorEvans, Thomas J.
dc.date.accessioned2019-01-24T12:30:06Z
dc.date.available2019-01-24T12:30:06Z
dc.date.issued2018-06-01
dc.identifier.citationGoswami , C , Fox , S , Holden , M , Connor , M , Leanord , A & Evans , T J 2018 , ' Genetic analysis of invasive Escherichia coli in Scotland reveals determinants of healthcare-associated versus community-acquired infections ' , Microbial Genomics , vol. 4 , no. 6 , 000190 . https://doi.org/10.1099/mgen.0.000190en
dc.identifier.issn2057-5858
dc.identifier.otherPURE: 257478039
dc.identifier.otherPURE UUID: c3014bc2-ad98-4480-863b-2c538c73d999
dc.identifier.otherScopus: 85059825011
dc.identifier.otherPubMed: 29932391
dc.identifier.otherORCID: /0000-0002-4958-2166/work/60196443
dc.identifier.otherWOS: 000439067200005
dc.identifier.urihttps://hdl.handle.net/10023/16931
dc.descriptionThe work was funded by the Scottish Executive via the Chief Scientist Office through the provision of a grant to establish the Scottish Healthcare Associated Infection Prevention Institute (SHAIPI).en
dc.description.abstractBacteraemia caused by Escherichia coli is a growing problem with a significant mortality. The factors that influence the acquisition and outcome of these infections are not clear. Here, we have linked detailed genetic data from the whole-genome sequencing of 162 bacteraemic isolates collected in Scotland, UK, in 2013-2015, with clinical data in order to delineate bacterial and host factors that influence the acquisition in hospital or the community, outcome and antibiotic resistance. We identified four major sequence types (STs) in these isolates: ST131, ST69, ST73 and ST95. Nearly 50% of the bacteraemic isolates had a urinary origin. ST69 was genetically distinct from the other STs, with significantly less sharing of accessory genes and with a distinct plasmid population. Virulence genes were widespread and diversely distributed between the dominant STs. ST131 was significantly associated with hospital-associated infections (HAIs), and ST69 with those from the community. However, there was no association of ST with outcome, although patients with HAI had a higher immediate mortality compared to those with community-associated infections (CAIs). Genome-wide association studies revealed genes involved in antibiotic persistence as significantly associated with HAIs and those encoding elements of a type VI secretion system with CAIs. Antibiotic resistance was common, and there were networks of correlated resistance genes and phenotypic antibiotic resistance. This study has revealed the complex interactions between the genotype of E. coli and its ability to cause bacteraemia, and some of the determinants influencing hospital or community acquisition. In part, these are shaped by antibiotic usage, but strain-specific factors are also important.
dc.format.extent15
dc.language.isoeng
dc.relation.ispartofMicrobial Genomicsen
dc.rightsCopyright © 2018 The Authors. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited.en
dc.subjectAntibiotic resistanceen
dc.subjectBacteraemiaen
dc.subjectGenome sequencingen
dc.subjectGenome-wide association studyen
dc.subjectQH426 Geneticsen
dc.subjectQR180 Immunologyen
dc.subjectDASen
dc.subject.lccQH426en
dc.subject.lccQR180en
dc.titleGenetic analysis of invasive Escherichia coli in Scotland reveals determinants of healthcare-associated versus community-acquired infectionsen
dc.typeJournal articleen
dc.description.versionPublisher PDFen
dc.contributor.institutionUniversity of St Andrews. School of Medicineen
dc.contributor.institutionUniversity of St Andrews. Infection and Global Health Divisionen
dc.contributor.institutionUniversity of St Andrews. Biomedical Sciences Research Complexen
dc.contributor.institutionUniversity of St Andrews. Infection Groupen
dc.identifier.doihttps://doi.org/10.1099/mgen.0.000190
dc.description.statusPeer revieweden


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