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A role for ColV plasmids in the evolution of pathogenic Escherichia coli ST58
iThree Institute, University of Technology Sydney, Ultimo, NSW, 2007, Australia.
iThree Institute, University of Technology Sydney, Ultimo, NSW, 2007, Australia.
Department of Animal Health and Antimicrobial Strategies, National Veterinary Institute (SVA), Uppsala, Sweden; Department of Microbiology, Public Health Agency of Sweden, Solna, Sweden.ORCID-id: 0000-0003-2219-2659
Wageningen Bioveterinary Research, Lelystad, Netherlands.
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2022 (engelsk)Inngår i: Nature Communications, E-ISSN 2041-1723, Vol. 13, artikkel-id 683Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Escherichia coli ST58 has recently emerged as a globally disseminated uropathogen that often progresses to sepsis. Unlike most pandemic extra-intestinal pathogenic E. coli (ExPEC), which belong to pathogenic phylogroup B2, ST58 belongs to the environmental/commensal phylogroup B1. Here, we present a pan-genomic analysis of a global collection of 752 ST58 isolates from diverse sources. We identify a large ST58 sub-lineage characterized by near ubiquitous carriage of ColV plasmids, which carry genes encoding virulence factors, and by a distinct accessory genome including genes typical of the Yersiniabactin High Pathogenicity Island. This sub-lineage includes three-quarters of all ExPEC sequences in our study and has a broad host range, although poultry and porcine sources predominate. By contrast, strains isolated from cattle often lack ColV plasmids. Our data indicate that ColV plasmid acquisition contributed to the divergence of the major ST58 sub-lineage, and different sub-lineages inhabit poultry, swine and cattle.

sted, utgiver, år, opplag, sider
Springer Nature , 2022. Vol. 13, artikkel-id 683
Emneord [en]
extended-spectrum, multidrug-resistant, antimicrobial resistance, p-fimbriae, enterobacteria, ceaevirulence, sequence, strains, clones, surveillance
HSV kategori
Identifikatorer
URN: urn:nbn:se:oru:diva-107638DOI: 10.1038/s41467-022-28342-4ISI: 000752207900029PubMedID: 35115531Scopus ID: 2-s2.0-85123974757OAI: oai:DiVA.org:oru-107638DiVA, id: diva2:1788372
Merknad

This study was partially funded by Czech Science Foundation Grant no. 18-23532S awarded to M.D. It was also supported by an Australian Government Medical Research Future Fund project (MRFF75873), the Australian Centre for Genomic Epidemiological Microbiology (AusGEM), a strategic research initiative between the New South Wales Department of Primary Industries and the University of Technology Sydney and Australian Research Council Linkage Project LP150100912.

Tilgjengelig fra: 2023-08-16 Laget: 2023-08-16 Sist oppdatert: 2023-11-06bibliografisk kontrollert

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