Genomic epidemiology reveals geographical clustering of multidrug-resistant Escherichia coli ST131 associated with bacteraemia in Wales

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作者
Rhys T. White
Matthew J. Bull
Clare R. Barker
Julie M. Arnott
Mandy Wootton
Lim S. Jones
Robin A. Howe
Mari Morgan
Melinda M. Ashcroft
Brian M. Forde
Thomas R. Connor
Scott A. Beatson
机构
[1] The University of Queensland,School of Chemistry and Molecular Biosciences
[2] The University of Queensland,Australian Infectious Disease Research Centre
[3] The University of Queensland,Australian Centre for Ecogenomics
[4] Cardiff University,Microbiomes, Microbes and Informatics Group, Organisms and Environment Division, School of Biosciences
[5] University Hospital of Wales,Public Health Wales Microbiology
[6] Public Health Wales,Healthcare Associated Infection, Antimicrobial Resistance & Prescribing Programme (HARP)
[7] 2 Capital Quarter,Department of Microbiology and Immunology
[8] The University of Melbourne at The Peter Doherty Institute for Infection and Immunity,The University of Queensland, UQ Centre for Clinical Research (UQCCR)
[9] Royal Brisbane & Women’s Hospital Campus,Public Health Genomics Programme
[10] Public Health Wales,Health Group
[11] 2 Capital Quarter,undefined
[12] Institute of Environmental Science and Research,undefined
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摘要
Antibiotic resistance is a significant global public health concern. Uropathogenic Escherichia coli sequence type (ST)131, a widely prevalent multidrug-resistant clone, is frequently associated with bacteraemia. This study investigates third-generation cephalosporin resistance in bloodstream infections caused by E. coli ST131. From 2013-2014 blood culture surveillance in Wales, 142 E. coli ST131 genomes were studied alongside global data. All three major ST131 clades were represented across Wales, with clade C/H30 predominant (n = 102/142, 71.8%). Consistent with global findings, Welsh strains of clade C/H30 contain β-lactamase genes from the blaCTX-M-1 group (n = 65/102, 63.7%), which confer resistance to third-generation cephalosporins. Most Welsh clade C/H30 genomes belonged to sub-clade C2/H30Rx (58.3%). A Wales-specific sub-lineage, named GB-WLS.C2, diverged around 1996-2000. An introduction to North Wales around 2002 led to a localised cluster by 2009, depicting limited genomic diversity within North Wales. This investigation emphasises the value of genomic epidemiology, allowing the detection of genetically similar strains in local areas, enabling targeted and timely public health interventions.
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