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大流行大肠杆菌 ST1193 的全球系统发育和 F 型毒力质粒携带情况。

Global Phylogeny and F Virulence Plasmid Carriage in Pandemic Escherichia coli ST1193.

机构信息

Australian Institute for Microbiology & Infection, University of Technology Sydney, Ultimo, New South Wales, Australia.

Asia-Pacific Centre for Animal Health, Department of Veterinary Biosciences, Melbourne Veterinary School, Faculty of Veterinary and Agricultural Sciences, University of Melbournegrid.1008.9, Parkville, Victoria, Australia.

出版信息

Microbiol Spectr. 2022 Dec 21;10(6):e0255422. doi: 10.1128/spectrum.02554-22. Epub 2022 Nov 21.

Abstract

Lower urinary tract, renal, and bloodstream infections caused by phylogroup B2 extraintestinal pathogenic Escherichia coli (ExPEC) are a leading cause of morbidity and mortality. ST1193 is a phylogroup B2, multidrug-resistant sequence type that has risen to prominence globally, but a comprehensive analysis of the F virulence plasmids it carries is lacking. We performed a phylogenomic analysis of ST1193 ( = 707) whole-genome sequences from EnteroBase using entries with comprehensive isolation metadata. The data set comprised isolates from humans ( = 634 [90%]), including 339 (48%) from extraintestinal infection sites, and isolates from companion animals, wastewater, and wildlife. Phylogenetic analyses combined with gene detection and genotyping resolved an ST1193 clade structure segregated by serotype and F plasmid carriage. Most F plasmids fell into one of three related plasmid subtypes: F:A1:B10 ( = 444 [65.97%]), F:A1:B1 ( = 84 [12.48%]), and F:A1:B20 ( = 80 [11.89%]), all of which carry the virulence genes colocalized with (), a trademark signature of F29:A:B10 subtype plasmids (pUTI89). To examine the phylogenetic relationship of these plasmids with pUTI89, complete sequences of F:A1:B1 and F:1:B20 plasmids were resolved. Unlike pUTI89, the most dominant and widely disseminated F plasmid that carries , F plasmids in ST1193 often carry a complex resistance region with an integron truncation () signature embedded within a structure assembled by IS. Plasmid analysis shows that ST1193 has F plasmids that carry - and ARG-encoding genes but lack regions and are likely derivatives of pUTI89. Further epidemiological investigation of ST1193 should seek to confirm its presence in human-associated environments and identify any potential agricultural links, which are currently lacking. We have generated an updated ST1193 phylogeny using publicly available sequences, reinforcing previous assertions that Escherichia coli ST1193 is a human-associated lineage, with many examples sourced from human extraintestinal infections. ST1193 from urban-adapted birds, wastewater, and companion animals are frequent, but isolates from animal agriculture are notably absent. Phylogenomic analysis identified several clades segregated by serogroup, all noted to carry highly similar F plasmids and antimicrobial resistance (AMR) signatures. Investigation of these plasmids revealed virulence regions with similarity to pUTI89, a key F virulence plasmid among dominant pandemic extraintestinal pathogenic E. coli lineages, and encoding a complex antibiotic resistance structure mobilized by IS This work has uncovered a series of F virulence plasmids in ST1193 and shows that the lineage mimics the host range and virulence attributes of other E. coli strains that carry pUTI89. These observations have significant ramifications for epidemiological source tracking of emerging and established pandemic ExPEC lineages.

摘要

下尿路、肾脏和血流感染由 B2 型肠外致病性大肠杆菌(ExPEC)引起,是发病率和死亡率的主要原因。ST1193 是一种 B2 型多药耐药性序列型,在全球范围内已经引起了关注,但对其携带的 F 型毒力质粒的全面分析还很缺乏。我们使用 EnteroBase 中具有全面分离元数据的 ST1193( = 707)全基因组序列进行了系统发育基因组学分析。该数据集包括来自人类( = 634 [90%])的分离株,包括 339 株(48%)来自肠外感染部位,以及来自伴侣动物、废水和野生动物的分离株。结合基因检测和基因分型的系统发育分析解决了按血清型和 F 质粒携带情况划分的 ST1193 进化枝结构。大多数 F 质粒属于三种相关质粒亚型之一:F:A1:B10( = 444 [65.97%])、F:A1:B1( = 84 [12.48%])和 F:A1:B20( = 80 [11.89%]),它们都携带与 colocalized 的毒力基因 (),这是 F29:A:B10 亚型质粒(pUTI89)的商标特征。为了研究这些质粒与 pUTI89 的系统发育关系,解析了 F:A1:B1 和 F:1:B20 质粒的完整序列。与 pUTI89 不同的是,携带 的最主要和广泛传播的 F 质粒,ST1193 中的 F 质粒通常携带一个复杂的耐药区,其中嵌入了一个由 IS 组装的结构。质粒分析表明,ST1193 具有携带 - 和 ARG 编码基因但缺乏 区的 F 质粒,可能是 pUTI89 的衍生物。进一步对 ST1193 的流行病学调查应寻求确认其在人类相关环境中的存在,并确定目前缺乏的任何潜在农业联系。我们使用公开可用的序列生成了一个更新的 ST1193 系统发育树,这进一步证实了之前的观点,即大肠杆菌 ST1193 是一种与人相关的谱系,其中许多分离株来自人类肠外感染。来自城市适应鸟类、废水和伴侣动物的 ST1193 很常见,但来自动物农业的分离株却明显缺失。系统基因组分析确定了几个按血清群分隔的进化枝,所有这些进化枝都被注意到携带高度相似的 F 质粒和抗生素耐药(AMR)特征。对这些质粒的研究揭示了与 pUTI89 相似的毒力区,pUTI89 是主导肠外致病性大肠杆菌谱系中的一种关键 F 毒力质粒,并编码由 IS 移动的复杂抗生素耐药结构。这项工作揭示了 ST1193 中的一系列 F 型毒力质粒,并表明该谱系模仿了携带 pUTI89 的其他大肠杆菌菌株的宿主范围和毒力特征。这些观察结果对新兴和已建立的肠外致病性大肠杆菌流行谱系的流行病学溯源具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a3c/9769970/2e81c018098d/spectrum.02554-22-f001.jpg

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