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Escherichia albertii, a novel human enteropathogen, colonizes rat enterocytes and translocates to extra-intestinal sites
Diarrhea is the second leading cause of death of children up to five years old in the developing countries. Among the etiological diarrheal agents are atypical enteropathogenic Escherichia coli (aEPEC), one of the diarrheagenic E. coli pathotypes that affects children and adults, even in developed c...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5298312/ https://www.ncbi.nlm.nih.gov/pubmed/28178312 http://dx.doi.org/10.1371/journal.pone.0171385 |
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author | Yamamoto, Denise Hernandes, Rodrigo T. Liberatore, Ana Maria A. Abe, Cecilia M. de Souza, Rodrigo B. Romão, Fabiano T. Sperandio, Vanessa Koh, Ivan H. Gomes, Tânia A. T. |
author_facet | Yamamoto, Denise Hernandes, Rodrigo T. Liberatore, Ana Maria A. Abe, Cecilia M. de Souza, Rodrigo B. Romão, Fabiano T. Sperandio, Vanessa Koh, Ivan H. Gomes, Tânia A. T. |
author_sort | Yamamoto, Denise |
collection | PubMed |
description | Diarrhea is the second leading cause of death of children up to five years old in the developing countries. Among the etiological diarrheal agents are atypical enteropathogenic Escherichia coli (aEPEC), one of the diarrheagenic E. coli pathotypes that affects children and adults, even in developed countries. Currently, genotypic and biochemical approaches have helped to demonstrate that some strains classified as aEPEC are actually E. albertii, a recently recognized human enteropathogen. Studies on particular strains are necessary to explore their virulence potential in order to further understand the underlying mechanisms of E. albertii infections. Here we demonstrated for the first time that infection of fragments of rat intestinal mucosa is a useful tool to study the initial steps of E. albertii colonization. We also observed that an E. albertii strain can translocate from the intestinal lumen to Mesenteric Lymph Nodes and liver in a rat model. Based on our finding of bacterial translocation, we investigated how E. albertii might cross the intestinal epithelium by performing infections of M-like cells in vitro to identify the potential in vivo translocation route. Altogether, our approaches allowed us to draft a general E. albertii infection route from the colonization till the bacterial spreading in vivo. |
format | Online Article Text |
id | pubmed-5298312 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-52983122017-02-17 Escherichia albertii, a novel human enteropathogen, colonizes rat enterocytes and translocates to extra-intestinal sites Yamamoto, Denise Hernandes, Rodrigo T. Liberatore, Ana Maria A. Abe, Cecilia M. de Souza, Rodrigo B. Romão, Fabiano T. Sperandio, Vanessa Koh, Ivan H. Gomes, Tânia A. T. PLoS One Research Article Diarrhea is the second leading cause of death of children up to five years old in the developing countries. Among the etiological diarrheal agents are atypical enteropathogenic Escherichia coli (aEPEC), one of the diarrheagenic E. coli pathotypes that affects children and adults, even in developed countries. Currently, genotypic and biochemical approaches have helped to demonstrate that some strains classified as aEPEC are actually E. albertii, a recently recognized human enteropathogen. Studies on particular strains are necessary to explore their virulence potential in order to further understand the underlying mechanisms of E. albertii infections. Here we demonstrated for the first time that infection of fragments of rat intestinal mucosa is a useful tool to study the initial steps of E. albertii colonization. We also observed that an E. albertii strain can translocate from the intestinal lumen to Mesenteric Lymph Nodes and liver in a rat model. Based on our finding of bacterial translocation, we investigated how E. albertii might cross the intestinal epithelium by performing infections of M-like cells in vitro to identify the potential in vivo translocation route. Altogether, our approaches allowed us to draft a general E. albertii infection route from the colonization till the bacterial spreading in vivo. Public Library of Science 2017-02-08 /pmc/articles/PMC5298312/ /pubmed/28178312 http://dx.doi.org/10.1371/journal.pone.0171385 Text en © 2017 Yamamoto et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Yamamoto, Denise Hernandes, Rodrigo T. Liberatore, Ana Maria A. Abe, Cecilia M. de Souza, Rodrigo B. Romão, Fabiano T. Sperandio, Vanessa Koh, Ivan H. Gomes, Tânia A. T. Escherichia albertii, a novel human enteropathogen, colonizes rat enterocytes and translocates to extra-intestinal sites |
title | Escherichia albertii, a novel human enteropathogen, colonizes rat enterocytes and translocates to extra-intestinal sites |
title_full | Escherichia albertii, a novel human enteropathogen, colonizes rat enterocytes and translocates to extra-intestinal sites |
title_fullStr | Escherichia albertii, a novel human enteropathogen, colonizes rat enterocytes and translocates to extra-intestinal sites |
title_full_unstemmed | Escherichia albertii, a novel human enteropathogen, colonizes rat enterocytes and translocates to extra-intestinal sites |
title_short | Escherichia albertii, a novel human enteropathogen, colonizes rat enterocytes and translocates to extra-intestinal sites |
title_sort | escherichia albertii, a novel human enteropathogen, colonizes rat enterocytes and translocates to extra-intestinal sites |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5298312/ https://www.ncbi.nlm.nih.gov/pubmed/28178312 http://dx.doi.org/10.1371/journal.pone.0171385 |
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