Medical, Molecular and Forensic Sciences, Murdoch University, Western Australia, Australia.
Department of Molecular and Cell Biology, University of Cape Town, Cape Town, South Africa.
mBio. 2019 Apr 16;10(2):e00446-19. doi: 10.1128/mBio.00446-19.
() sequence type 11 (ST11) is well established in production animal populations worldwide and contributes considerably to the global burden of infection (CDI) in humans. Increasing evidence of shared ancestry and genetic overlap of PCR ribotype 078 (RT078), the most common ST11 sublineage, between human and animal populations suggests that CDI may be a zoonosis. We performed whole-genome sequencing (WGS) on a collection of 207 ST11 and closely related ST258 isolates of human and veterinary/environmental origin, comprising 16 RTs collected from Australia, Asia, Europe, and North America. Core genome single nucleotide variant (SNV) analysis identified multiple intraspecies and interspecies clonal groups (isolates separated by ≤2 core genome SNVs) in all the major RT sublineages: 078, 126, 127, 033, and 288. Clonal groups comprised isolates spread across different states, countries, and continents, indicative of reciprocal long-range dissemination and possible zoonotic/anthroponotic transmission. Antimicrobial resistance genotypes and phenotypes varied across host species, geographic regions, and RTs and included macrolide/lincosamide resistance (Tn []), tetracycline resistance (Tn [] and Tn []), and fluoroquinolone resistance (/ mutations), as well as numerous aminoglycoside resistance cassettes. The population was defined by a large "open" pan-genome (10,378 genes), a remarkably small core genome of 2,058 genes (only 19.8% of the gene pool), and an accessory genome containing a large and diverse collection of important prophages of the and This study provides novel insights into strain relatedness and genetic variability of ST11, a lineage of global One Health importance. Historically, () has been associated with life-threatening diarrhea in hospitalized patients. Increasing rates of infection (CDI) in the community suggest exposure to reservoirs outside the hospital, including animals, the environment, or food. sequence type 11 (ST11) is known to infect/colonize livestock worldwide and comprises multiple ribotypes, many of which cause disease in humans, suggesting CDI may be a zoonosis. Using high-resolution genomics, we investigated the evolution and zoonotic potential of ST11 and a new closely related ST258 lineage sourced from diverse origins. We found multiple intra- and interspecies clonal transmission events in all ribotype sublineages. Clones were spread across multiple continents, often without any health care association, indicative of zoonotic/anthroponotic long-range dissemination in the community. ST11 possesses a massive pan-genome and numerous clinically important antimicrobial resistance elements and prophages, which likely contribute to the success of this globally disseminated lineage of One Health importance.
() 序列类型 11(ST11)在全球的生产动物种群中已经得到很好的确立,并对人类中感染(CDI)的全球负担有很大贡献。PCR 核糖型 078(RT078)的共同祖先和遗传重叠的证据越来越多,RT078 是最常见的 ST11 亚系,这表明 CDI 可能是一种人畜共患病。我们对来自澳大利亚、亚洲、欧洲和北美的 16 个 RT 收集的 207 株人类和兽医/环境来源的 ST11 和密切相关的 ST258 分离株进行了全基因组测序(WGS)。核心基因组单核苷酸变异(SNV)分析确定了所有主要 RT 亚系中的多个种内和种间克隆群(核心基因组 SNV 差异≤2 的分离株):078、126、127、033 和 288。克隆群包括分布在不同州、国家和大陆的分离株,表明存在相互的长距离传播和可能的人畜共患病/人间传播。抗生素耐药基因型和表型在宿主物种、地理区域和 RT 之间存在差异,包括大环内酯/林可酰胺耐药(Tn [])、四环素耐药(Tn [] 和 Tn [])和氟喹诺酮耐药(/ 突变),以及许多氨基糖苷类耐药盒。该种群由一个大型的“开放”泛基因组(10378 个基因)、一个非常小的核心基因组(2058 个基因,仅占基因库的 19.8%)和一个包含大量重要的 和 噬菌体的辅助基因组定义。这项研究提供了关于 ST11 的菌株相关性和遗传变异性的新见解,ST11 是具有全球“同一健康”重要性的谱系。历史上, () 与住院患者的危及生命的腹泻有关。社区中不断增加的感染(CDI)率表明,除医院外,还可能接触到动物、环境或食物等其他 储主。 序列类型 11(ST11)在全球范围内被发现感染/定植于牲畜,包括多种核糖型,其中许多会导致人类患病,这表明 CDI 可能是一种人畜共患病。本研究使用高分辨率基因组学技术,研究了 ST11 及其新的密切相关的 ST258 谱系的进化和人畜共患潜力,这些谱系来自于不同的来源。我们在所有核糖型亚系中都发现了种内和种间的克隆传播事件。克隆株分布在多个大洲,通常与任何医疗保健都没有关联,表明在社区中存在人畜共患/人间的长距离传播。ST11 拥有庞大的泛基因组和许多具有临床重要性的抗生素耐药元件和噬菌体,这可能有助于该谱系在全球范围内的传播和成功。