Magdalena Nüesch-Inderbinen , Marc J.A. Stevens , Nicole Cernela , Andrea Müller , Michael Biggel , Roger Stephan
{"title":"人类感染产志贺毒素大肠杆菌O91血清群的毒力因子分布、耐药基因及系统发育相关性","authors":"Magdalena Nüesch-Inderbinen , Marc J.A. Stevens , Nicole Cernela , Andrea Müller , Michael Biggel , Roger Stephan","doi":"10.1016/j.ijmm.2021.151541","DOIUrl":null,"url":null,"abstract":"<div><p>Shiga toxin-producing <em>Escherichia coli</em> (STEC) belonging to the serogroup O91 are among the most common non-O157 STEC serogroups associated with human illness in Europe. This study aimed to analyse the virulence factors, antimicrobial resistance genes and phylogenetic relatedness among 48 clinical STEC O91 isolates collected during 2003–2019 in Switzerland. The isolates were subjected to whole genome sequencing using short-read sequencing technologies and a subset of isolates additionally to long-read sequencing. They belonged to O91:H10 (n<!--> <!-->=<!--> <!-->6), O91:H14 (n<!--> <!-->=<!--> <!-->40), and O91:H21 (n<!--> <!-->=<!--> <!-->2). Multilocus sequence typing showed that the O91:H10 isolates all belonged to sequence type (ST)641, while the O91:H14 isolates were assigned to ST33, ST9700, or were non-typeable. Both O91:H21 isolates belonged to ST442. Shiga toxin gene <em>stx1a</em> was the most common Shiga toxin gene subtype among the isolates, followed by <em>stx2b</em>, <em>stx2d</em> and <em>stx2a</em>. All isolates were LEE-negative and carried one or two copies of the IrgA adhesin gene <em>iha</em>. In a subset of long-read sequenced isolates, modules of the Locus of Adhesion and Autoaggregation pathogenicity island (LAA-PAI) carrying <em>iha</em> and other genes such as <em>hes</em>, <em>lesP</em> or <em>agn43</em> were identified. A large proportion of STEC O91:H14 carried the subtilase cytotoxin gene <em>subA</em>, colicin genes (<em>cba</em>, <em>cea</em>, <em>cib</em> and <em>cma</em>) or microcin genes (<em>mcmA</em>, <em>mchB</em>, <em>mchC</em> and <em>mchF</em>). STEC O91:H14 were further distinguished from STEC O91:H10/H21 by one or more virulence factors found in extraintestinal pathogenic <em>E. coli</em> (ExPEC), including <em>hlyF</em>, <em>iucC/iutA</em>, <em>kpsE</em> and <em>traT</em>. The <em>hlyF</em> gene was identified on a novel mosaic plasmid that was unrelated to <em>hlyF</em>+ plasmids described previously in STEC. Core genome phylogenetic analysis revealed that STEC O91:H10 and STEC O91:H21 were clonally conserved, whereas STEC O91:H14 were clonally diverse. Among three STEC O91:H14 isolates, a number of resistance genes were identified, including genes that mediate resistance to aminoglycosides (<em>aadA</em>, <em>aadA2</em>, <em>aadA9</em>, <em>aadA23</em>, <em>aph(3'')-Ib</em> and <em>aph(6)-Id</em>), chloramphenicol (<em>cmlA</em>), sulphonamides (<em>sul2</em> and <em>sul3</em>), and trimethoprim (<em>drfA12</em>). Our data contribute to understanding the genetic diversity and differing levels of virulence potential within the STEC O91 serogroup.</p></div>","PeriodicalId":50312,"journal":{"name":"International Journal of Medical Microbiology","volume":"311 8","pages":"Article 151541"},"PeriodicalIF":4.5000,"publicationDate":"2021-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1438422121000709/pdfft?md5=d604d4c8bc20494f2f46e229cc299611&pid=1-s2.0-S1438422121000709-main.pdf","citationCount":"6","resultStr":"{\"title\":\"Distribution of virulence factors, antimicrobial resistance genes and phylogenetic relatedness among Shiga toxin-producing Escherichia coli serogroup O91 from human infections\",\"authors\":\"Magdalena Nüesch-Inderbinen , Marc J.A. Stevens , Nicole Cernela , Andrea Müller , Michael Biggel , Roger Stephan\",\"doi\":\"10.1016/j.ijmm.2021.151541\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Shiga toxin-producing <em>Escherichia coli</em> (STEC) belonging to the serogroup O91 are among the most common non-O157 STEC serogroups associated with human illness in Europe. This study aimed to analyse the virulence factors, antimicrobial resistance genes and phylogenetic relatedness among 48 clinical STEC O91 isolates collected during 2003–2019 in Switzerland. The isolates were subjected to whole genome sequencing using short-read sequencing technologies and a subset of isolates additionally to long-read sequencing. They belonged to O91:H10 (n<!--> <!-->=<!--> <!-->6), O91:H14 (n<!--> <!-->=<!--> <!-->40), and O91:H21 (n<!--> <!-->=<!--> <!-->2). Multilocus sequence typing showed that the O91:H10 isolates all belonged to sequence type (ST)641, while the O91:H14 isolates were assigned to ST33, ST9700, or were non-typeable. Both O91:H21 isolates belonged to ST442. Shiga toxin gene <em>stx1a</em> was the most common Shiga toxin gene subtype among the isolates, followed by <em>stx2b</em>, <em>stx2d</em> and <em>stx2a</em>. All isolates were LEE-negative and carried one or two copies of the IrgA adhesin gene <em>iha</em>. In a subset of long-read sequenced isolates, modules of the Locus of Adhesion and Autoaggregation pathogenicity island (LAA-PAI) carrying <em>iha</em> and other genes such as <em>hes</em>, <em>lesP</em> or <em>agn43</em> were identified. A large proportion of STEC O91:H14 carried the subtilase cytotoxin gene <em>subA</em>, colicin genes (<em>cba</em>, <em>cea</em>, <em>cib</em> and <em>cma</em>) or microcin genes (<em>mcmA</em>, <em>mchB</em>, <em>mchC</em> and <em>mchF</em>). STEC O91:H14 were further distinguished from STEC O91:H10/H21 by one or more virulence factors found in extraintestinal pathogenic <em>E. coli</em> (ExPEC), including <em>hlyF</em>, <em>iucC/iutA</em>, <em>kpsE</em> and <em>traT</em>. The <em>hlyF</em> gene was identified on a novel mosaic plasmid that was unrelated to <em>hlyF</em>+ plasmids described previously in STEC. Core genome phylogenetic analysis revealed that STEC O91:H10 and STEC O91:H21 were clonally conserved, whereas STEC O91:H14 were clonally diverse. Among three STEC O91:H14 isolates, a number of resistance genes were identified, including genes that mediate resistance to aminoglycosides (<em>aadA</em>, <em>aadA2</em>, <em>aadA9</em>, <em>aadA23</em>, <em>aph(3'')-Ib</em> and <em>aph(6)-Id</em>), chloramphenicol (<em>cmlA</em>), sulphonamides (<em>sul2</em> and <em>sul3</em>), and trimethoprim (<em>drfA12</em>). Our data contribute to understanding the genetic diversity and differing levels of virulence potential within the STEC O91 serogroup.</p></div>\",\"PeriodicalId\":50312,\"journal\":{\"name\":\"International Journal of Medical Microbiology\",\"volume\":\"311 8\",\"pages\":\"Article 151541\"},\"PeriodicalIF\":4.5000,\"publicationDate\":\"2021-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S1438422121000709/pdfft?md5=d604d4c8bc20494f2f46e229cc299611&pid=1-s2.0-S1438422121000709-main.pdf\",\"citationCount\":\"6\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Medical Microbiology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1438422121000709\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Medical Microbiology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1438422121000709","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
Distribution of virulence factors, antimicrobial resistance genes and phylogenetic relatedness among Shiga toxin-producing Escherichia coli serogroup O91 from human infections
Shiga toxin-producing Escherichia coli (STEC) belonging to the serogroup O91 are among the most common non-O157 STEC serogroups associated with human illness in Europe. This study aimed to analyse the virulence factors, antimicrobial resistance genes and phylogenetic relatedness among 48 clinical STEC O91 isolates collected during 2003–2019 in Switzerland. The isolates were subjected to whole genome sequencing using short-read sequencing technologies and a subset of isolates additionally to long-read sequencing. They belonged to O91:H10 (n = 6), O91:H14 (n = 40), and O91:H21 (n = 2). Multilocus sequence typing showed that the O91:H10 isolates all belonged to sequence type (ST)641, while the O91:H14 isolates were assigned to ST33, ST9700, or were non-typeable. Both O91:H21 isolates belonged to ST442. Shiga toxin gene stx1a was the most common Shiga toxin gene subtype among the isolates, followed by stx2b, stx2d and stx2a. All isolates were LEE-negative and carried one or two copies of the IrgA adhesin gene iha. In a subset of long-read sequenced isolates, modules of the Locus of Adhesion and Autoaggregation pathogenicity island (LAA-PAI) carrying iha and other genes such as hes, lesP or agn43 were identified. A large proportion of STEC O91:H14 carried the subtilase cytotoxin gene subA, colicin genes (cba, cea, cib and cma) or microcin genes (mcmA, mchB, mchC and mchF). STEC O91:H14 were further distinguished from STEC O91:H10/H21 by one or more virulence factors found in extraintestinal pathogenic E. coli (ExPEC), including hlyF, iucC/iutA, kpsE and traT. The hlyF gene was identified on a novel mosaic plasmid that was unrelated to hlyF+ plasmids described previously in STEC. Core genome phylogenetic analysis revealed that STEC O91:H10 and STEC O91:H21 were clonally conserved, whereas STEC O91:H14 were clonally diverse. Among three STEC O91:H14 isolates, a number of resistance genes were identified, including genes that mediate resistance to aminoglycosides (aadA, aadA2, aadA9, aadA23, aph(3'')-Ib and aph(6)-Id), chloramphenicol (cmlA), sulphonamides (sul2 and sul3), and trimethoprim (drfA12). Our data contribute to understanding the genetic diversity and differing levels of virulence potential within the STEC O91 serogroup.
期刊介绍:
Pathogen genome sequencing projects have provided a wealth of data that need to be set in context to pathogenicity and the outcome of infections. In addition, the interplay between a pathogen and its host cell has become increasingly important to understand and interfere with diseases caused by microbial pathogens. IJMM meets these needs by focussing on genome and proteome analyses, studies dealing with the molecular mechanisms of pathogenicity and the evolution of pathogenic agents, the interactions between pathogens and host cells ("cellular microbiology"), and molecular epidemiology. To help the reader keeping up with the rapidly evolving new findings in the field of medical microbiology, IJMM publishes original articles, case studies and topical, state-of-the-art mini-reviews in a well balanced fashion. All articles are strictly peer-reviewed. Important topics are reinforced by 2 special issues per year dedicated to a particular theme. Finally, at irregular intervals, current opinions on recent or future developments in medical microbiology are presented in an editorial section.