4.7 Article

F Plasmid Lineages in Escherichia coli ST95: Implications for Host Range, Antibiotic Resistance, and Zoonoses

期刊

MSYSTEMS
卷 7, 期 1, 页码 -

出版社

AMER SOC MICROBIOLOGY

关键词

ST131; ST73; ST95; E; coli; APEC; antibiotic resistance; antimicrobial resistance; ColV; Escherichia coli; ExPEC; plasmid; pUTI89

资金

  1. Australian Centre for Genomic Epidemiological Microbiology (AusGEM)
  2. Medical Research Future Fund Frontier Health and Medical Research Program [MRFF75873]

向作者/读者索取更多资源

Escherichia coli sequence type 95 (ST95) is a pathogenic bacteria known for causing illness in humans and poultry. A study analyzed the genome of 668 ST95 isolates and identified different clades based on the presence of specific plasmids. It was found that certain plasmids were predominantly present in isolates from humans, while others were found in isolates from both humans and poultry. Additionally, the study observed similar patterns in a diverse collection of 34,176 E. coli genomes. This research highlights the importance of plasmids in influencing the host range and zoonotic potential of E. coli.
Escherichia coli sequence type 95 (ST95) is an extraintestinal pathogenic E. coli (ExPEC) renowned for its ability to cause significant morbidity and mortality in humans and poultry. A core genome analysis of 668 ST95 isolates generated 10 clades (A to J), 5 of which are reported here for the first time. F plasmid replicon sequence typing showed that almost a third (178/668 [27%]) of the collection carry pUTI89 (F29:B10) and were restricted to clade A and a sublineage of clade B. In con -trast, almost half (328/668 [49%]) of the collection across multiple clades harbor ColV plasmids (multiple F types). Strikingly, ST95 lineages with pUTI89 were almost exclusively from humans, while ColV+ ST95 lineages were sourced from poultry and humans. Clade I was notable because it comprises temporally and geographically matched ColV+ isolates sourced from human and retail poultry meat, suggesting interspecies transmission via food. Clade F contained ST95 isolates of bovine origin, none of which carried ColV or pUTI89 plasmids. Remarkably, an analysis of a cohort of 34,176 E. coli isolates comprising 2,570 sequence types mirrored what was observed in ST95: (i) pUTI89 was overwhelmingly linked to E. coli sourced from humans but almost entirely absent from 13,027 E. coli isolates recovered from poul-try, pigs, and cattle, and (ii) E. coli isolates harboring ColV plasmids were from multi-ple sources, including humans, poultry, and swine. Overall, our data suggest that F plasmids influence E. coli host range, clade structure, and zoonotic potential in ST95 and ExPEC more broadly. IMPORTANCE E. coli ST95 is one of five dominant ExPEC lineages globally and noted for causing urinary tract and bloodstream infections and neonatal meningitis in humans and colibacillosis in poultry. Using high-resolution phylogenomics, we show that F replicon sequence type is linked to ST95 clade structure and zoonotic poten-tial. Specifically, human centric ST95 clades overwhelmingly harbor F29:B10 (pUTI89) plasmids, while clades carrying both human-and poultry-sourced isolates are typi-cally ColV+ with multiple replicon types. Importantly, several clades identified clonal ColV+ ST95 isolates from human and poultry sources, but clade I, which housed tem-porally and spatially matched isolates, provided the most robust evidence. Notably, patterns of association of F replicon types with E. coli host were mirrored within a diverse collection of 34,176 E. coli genomes. Our studies indicate that the role of food animals as a source of human ExPEC disease is complex and warrants further investigation.

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