Title
Cumulative acquisition of pathogenicity islands has shaped virulence potential and contributed to the emergence of LEE-negative Shiga toxin-producing Escherichia coli strains
Date Issued
01 January 2019
Access level
open access
Resource Type
journal article
Author(s)
Montero D.A.
Canto F.D.
Velasco J.
Colello R.
Padola N.L.
Salazar J.C.
Martin C.S.
Oñate A.
Blanco J.
Rasko D.A.
Puente J.L.
Scheutz F.
Franz E.
Vidal R.M.
Universidad Nacional Autónoma de México
Publisher(s)
Taylor and Francis Ltd.
Abstract
Shiga toxin-producing Escherichia coli (STEC) are foodborne pathogens causing severe gastroenteritis, which may lead to hemolytic uremic syndrome. The Locus of Enterocyte Effacement (LEE), a Pathogenicity Island (PAI), is a major determinant of intestinal epithelium attachment of a group of STEC strains; however, the virulence repertoire of STEC strains lacking LEE, has not been fully characterized. The incidence of LEE-negative STEC strains has increased in several countries, highlighting the relevance of their study. In order to gain insights into the basis for the emergence of LEE-negative STEC strains, we performed a large-scale genomic analysis of 367 strains isolated worldwide from humans, animals, food and the environment. We identified uncharacterized genomic islands, including two PAIs and one Integrative Conjugative Element. Additionally, the Locus of Adhesion and Autoaggregation (LAA) was the most prevalent PAI among LEE-negative strains and we found that it contributes to colonization of the mice intestine. Our comprehensive and rigorous comparative genomic and phylogenetic analyses suggest that the accumulative acquisition of PAIs has played an important, but currently unappreciated role, in the evolution of virulence in these strains. This study provides new knowledge on the pathogenicity of LEE-negative STEC strains and identifies molecular markers for their epidemiological surveillance.
Start page
486
End page
502
Volume
8
Issue
1
Language
English
OCDE Knowledge area
VirologÃa
GastroenterologÃa, HepatologÃa
Subjects
Scopus EID
2-s2.0-85064118989
PubMed ID
Source
Emerging Microbes and Infections
ISSN of the container
22221751
DOI of the container
10.1080/22221751.2019.1595985
Source funding
Fondo Nacional de Desarrollo CientÃfico y Tecnológico
Federación Española de Enfermedades Raras
Instituto de Salud Carlos III
ConsellerÃa de Cultura, Educación e Ordenación Universitaria, Xunta de Galicia
European Regional Development Fund
Ministerio de EconomÃa, Industria y Competitividad, Gobierno de España
Sponsor(s)
This study was supported by FONDECYT grant 1161161 to R. Vidal and CONICYT-PCHA/2014-63140238 fellowship to D. Montero. Work at USC-LREC was supported by Project PI16/01477 from Plan Estatal de I+D+I 2013-2016, Insti-tuto de Salud Carlos III, Subdirección General de Evaluación y Fomento de la Investigación and FEDER, Ministerio de Economia, Industria y Competitividad, Gobierno de España and Project ED431C 2017/57 from the ConsellerÃa de Cul-tura, Educación e Ordenación Universitaria, Xunta de Galicia and FEDER. Fondecyt 11150966 to Felipe Del Canto. Consejo Nacional de Ciencia y TecnologÃa; [Fondo Nacional de Desarrollo CientÃfico y Tecnológico].
This study was supported by FONDECYT grant 1161161 to R. Vidal and CONICYT-PCHA/2014-63140238 fellowship to D. Montero. Work at USC-LREC was supported by Project PI16/01477 from Plan Estatal de I+D+I 2013-2016, Instituto de Salud Carlos III, Subdirección General de Evaluación y Fomento de la Investigación and FEDER, Ministerio de Economia, Industria y Competitividad, Gobierno de España and Project ED431C 2017/57 from the ConsellerÃa de Cultura, Educación e Ordenación Universitaria, Xunta de Galicia and FEDER. Fondecyt 11150966 to Felipe Del Canto. Consejo Nacional de Ciencia y TecnologÃa; [Fondo Nacional de Desarrollo CientÃfico y Tecnológico]. We thank Dr. Carlos Smith and Anne Lagomarcino for their careful review and edition of the manuscript and helpful discussions.
Sources of information:
Directorio de Producción CientÃfica
Scopus