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Genetic characterization of commensal Escherichia coli isolated from laboratory rodents

BACKGROUND: Escherichia coli, a commensal in the intestines of vertebrates, is capable of colonizing many different hosts and the environment. Commensal E. coli strains are believed to be the precursor of pathogenic strains by means of acquisition of antimicrobial resistant and virulence genes. Labo...

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Autores principales: Loong, Shih Keng, Mahfodz, Nur Hidayana, Che Mat Seri, Nurul Asma Anati, Mohamad Wali, Haryanti Azura, Abd Gani, Syahar Amir, Wong, Pooi-Fong, AbuBakar, Sazaly
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4940358/
https://www.ncbi.nlm.nih.gov/pubmed/27462483
http://dx.doi.org/10.1186/s40064-016-2745-9
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author Loong, Shih Keng
Mahfodz, Nur Hidayana
Che Mat Seri, Nurul Asma Anati
Mohamad Wali, Haryanti Azura
Abd Gani, Syahar Amir
Wong, Pooi-Fong
AbuBakar, Sazaly
author_facet Loong, Shih Keng
Mahfodz, Nur Hidayana
Che Mat Seri, Nurul Asma Anati
Mohamad Wali, Haryanti Azura
Abd Gani, Syahar Amir
Wong, Pooi-Fong
AbuBakar, Sazaly
author_sort Loong, Shih Keng
collection PubMed
description BACKGROUND: Escherichia coli, a commensal in the intestines of vertebrates, is capable of colonizing many different hosts and the environment. Commensal E. coli strains are believed to be the precursor of pathogenic strains by means of acquisition of antimicrobial resistant and virulence genes. Laboratory rodents are inherently susceptible to numerous known infectious agents, which could transfer virulence determinants to commensal E. coli. Hence, in this study, the genetic structure of commensal E. coli found in laboratory rodents and their antimicrobial resistance profiles were investigated. RESULTS: E. coli strains belonging to phylogroup A were the predominant strain obtained from the animals used in the study. Four novel sequence types (ST746, ST747, ST748 and ST749) were discovered using the multi locus sequence typing, together with one common ST357 in the gastrointestinal tract, liver and, the trachea and lung. Serotyping demonstrated that these commensal E. coli strains were non-Shiga toxin-producers. Phenotypic and genotypic analyses of extended spectrum beta lactamases were also negative. CONCLUSIONS: These findings implied that the E. coli strains recovered from the laboratory rodents were truly commensal in nature. Further study is required to investigate the possible influence of gender on the susceptibility of hosts to E. coli colonization in laboratory rodents. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40064-016-2745-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-49403582016-07-26 Genetic characterization of commensal Escherichia coli isolated from laboratory rodents Loong, Shih Keng Mahfodz, Nur Hidayana Che Mat Seri, Nurul Asma Anati Mohamad Wali, Haryanti Azura Abd Gani, Syahar Amir Wong, Pooi-Fong AbuBakar, Sazaly Springerplus Research BACKGROUND: Escherichia coli, a commensal in the intestines of vertebrates, is capable of colonizing many different hosts and the environment. Commensal E. coli strains are believed to be the precursor of pathogenic strains by means of acquisition of antimicrobial resistant and virulence genes. Laboratory rodents are inherently susceptible to numerous known infectious agents, which could transfer virulence determinants to commensal E. coli. Hence, in this study, the genetic structure of commensal E. coli found in laboratory rodents and their antimicrobial resistance profiles were investigated. RESULTS: E. coli strains belonging to phylogroup A were the predominant strain obtained from the animals used in the study. Four novel sequence types (ST746, ST747, ST748 and ST749) were discovered using the multi locus sequence typing, together with one common ST357 in the gastrointestinal tract, liver and, the trachea and lung. Serotyping demonstrated that these commensal E. coli strains were non-Shiga toxin-producers. Phenotypic and genotypic analyses of extended spectrum beta lactamases were also negative. CONCLUSIONS: These findings implied that the E. coli strains recovered from the laboratory rodents were truly commensal in nature. Further study is required to investigate the possible influence of gender on the susceptibility of hosts to E. coli colonization in laboratory rodents. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40064-016-2745-9) contains supplementary material, which is available to authorized users. Springer International Publishing 2016-07-11 /pmc/articles/PMC4940358/ /pubmed/27462483 http://dx.doi.org/10.1186/s40064-016-2745-9 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Research
Loong, Shih Keng
Mahfodz, Nur Hidayana
Che Mat Seri, Nurul Asma Anati
Mohamad Wali, Haryanti Azura
Abd Gani, Syahar Amir
Wong, Pooi-Fong
AbuBakar, Sazaly
Genetic characterization of commensal Escherichia coli isolated from laboratory rodents
title Genetic characterization of commensal Escherichia coli isolated from laboratory rodents
title_full Genetic characterization of commensal Escherichia coli isolated from laboratory rodents
title_fullStr Genetic characterization of commensal Escherichia coli isolated from laboratory rodents
title_full_unstemmed Genetic characterization of commensal Escherichia coli isolated from laboratory rodents
title_short Genetic characterization of commensal Escherichia coli isolated from laboratory rodents
title_sort genetic characterization of commensal escherichia coli isolated from laboratory rodents
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4940358/
https://www.ncbi.nlm.nih.gov/pubmed/27462483
http://dx.doi.org/10.1186/s40064-016-2745-9
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