Hazen Tracy H, Nagaraj Sushma, Sen Sunil, Permala-Booth Jasnehta, Del Canto Felipe, Vidal Roberto, Barry Eileen M, Bitoun Jacob P, Chen Wilbur H, Tennant Sharon M, Rasko David A
Institute for Genome Sciences, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Department of Microbiology and Immunology, University of Maryland School of Medicine, Baltimore, Maryland, USA.
mSystems. 2019 Jan 15;4(1). doi: 10.1128/mSystems.00329-18. eCollection 2019 Jan-Feb.
Enterotoxigenic Escherichia coli (ETEC) is a significant cause of childhood diarrhea and is a leading cause of traveler's diarrhea. ETEC strains encoding the heat-stable enterotoxin (ST) are more often associated with childhood diarrhea than ETEC strains that encode only the heat-labile enterotoxin (LT). Colonization factors (CFs) also have a demonstrated role in ETEC virulence, and two of the most prevalent CFs among ETEC that have caused diarrhea are colonization factor antigen I (CFA/I) and CS6. In the current report, we describe the genomes of 269 CS6- or CFA/I-encoding ST-only ETEC isolates that were associated with human diarrhea. While the CS6 and CFA/I ETEC were identified in at least 13 different ETEC genomic lineages, a majority (85%; 229/269) were identified in only six lineages. Complete genome sequencing of selected isolates demonstrated that a conserved plasmid contributed to the dissemination of CFA/I whereas at least five distinct plasmids were involved in the dissemination of ST and/or CS6. Additionally, there were differences in gene content between CFA/I and CS6 ETEC at the phylogroup and lineage levels and in association with their geographic location of isolation as well as lineage-related differences in ST production. Thus, we demonstrate that genomically diverse E. coli strains have acquired ST, as well as CFA/I or CS6, via one or more plasmids and that, in some cases, isolates of a particular lineage or geographic location have undergone additional modifications to their genome content. These findings will aid investigations of virulence and the development of improved diagnostics and vaccines against this important human diarrheal pathogen. Comparative genomics and functional characterization were used to analyze a global collection of CFA/I and CS6 ST-only ETEC isolates associated with human diarrhea, demonstrating differences in the genomic content of CFA/I and CS6 isolates related to CF type, lineage, and geographic location of isolation and also lineage-related differences in ST production. Complete genome sequencing of selected CFA/I and CS6 isolates enabled descriptions of a highly conserved ST-positive (ST) CFA/I plasmid and of at least five diverse ST and/or CS6 plasmids among the CS6 ETEC isolates. There is currently no approved vaccine for ST-only ETEC, or for any ETEC for that matter, and as such, the current report provides functional verification of ST and CF production and antimicrobial susceptibility testing and an in-depth genomic characterization of a collection of isolates that could serve as representatives of CFA/I- or CS6-encoding ST-only ETEC strains for future studies of ETEC pathogenesis, vaccine studies, and/or clinical trials.
产肠毒素大肠杆菌(ETEC)是儿童腹泻的重要病因,也是旅行者腹泻的主要病因。编码热稳定肠毒素(ST)的ETEC菌株比仅编码热不稳定肠毒素(LT)的ETEC菌株更常与儿童腹泻相关。定植因子(CFs)在ETEC毒力中也发挥着作用,在引发腹泻的ETEC中,两种最常见的CF是定植因子抗原I(CFA/I)和CS6。在本报告中,我们描述了269株仅编码ST的、与人类腹泻相关的CS6或CFA/I编码的ETEC分离株的基因组。虽然在至少13种不同的ETEC基因组谱系中鉴定出了CS6和CFA/I ETEC,但大多数(85%;229/269)仅在6种谱系中被鉴定出。对选定分离株的全基因组测序表明,一个保守质粒促成了CFA/I的传播,而至少5种不同的质粒参与了ST和/或CS6的传播。此外,CFA/I和CS6 ETEC在菌群和谱系水平上的基因含量存在差异,并且与其分离的地理位置以及ST产生的谱系相关差异有关。因此,我们证明了基因组多样的大肠杆菌菌株通过一个或多个质粒获得了ST以及CFA/I或CS6,并且在某些情况下,特定谱系或地理位置的分离株对其基因组内容进行了额外的修饰。这些发现将有助于对这种重要的人类腹泻病原体的毒力进行研究,并有助于开发改进的诊断方法和疫苗。比较基因组学和功能表征被用于分析与人类腹泻相关的全球CFA/I和CS6仅编码ST的ETEC分离株集合,证明了CFA/I和CS6分离株在基因组内容上与CF类型、谱系和分离地理位置相关的差异,以及ST产生的谱系相关差异。对选定的CFA/I和CS6分离株进行全基因组测序,能够描述一种高度保守的ST阳性(ST)CFA/I质粒以及CS6 ETEC分离株中至少5种不同的ST和/或CS6质粒。目前尚无针对仅编码ST的ETEC或任何ETEC的批准疫苗,因此,本报告提供了ST和CF产生的功能验证以及抗菌药敏试验,并对一组分离株进行了深入的基因组表征,这些分离株可作为仅编码CFA/I或CS6的ST的ETEC菌株的代表,用于未来ETEC发病机制研究、疫苗研究和/或临床试验。