Escherichia albertii, a novel human enteropathogen, colonizes rat enterocytes and translocates to extra-intestinal sites
Autor: | Rodrigo T. Hernandes, Ivan Hong Jun Koh, Ana Maria Alvim Liberatore, Vanessa Sperandio, Cecilia M. Abe, Denise Yamamoto, Fabiano T. Romão, Rodrigo Barbosa de Souza, Tânia A. T. Gomes |
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Přispěvatelé: | Universidade Federal de São Paulo (UNIFESP), Universidade Estadual Paulista (Unesp), Instituto Butantan, University of Texas Southwestern Medical Center |
Jazyk: | angličtina |
Rok vydání: | 2017 |
Předmět: |
Bacterial Diseases
0301 basic medicine Cell Lines lcsh:Medicine medicine.disease_cause Epithelium Escherichia albertii Electricity Intestinal mucosa Medicine and Health Sciences Type III Secretion Systems Electron Microscopy Intestinal Mucosa lcsh:Science Cells Cultured Microscopy Multidisciplinary Bacterial Gastroenteritis Virulence Physics Enterobacteriaceae Infections Cell Differentiation Intestinal epithelium Gastroenteritis Mutant Strains Infectious Diseases Shigellosis Physical Sciences Female Biological Cultures Scanning Electron Microscopy Anatomy Research Article Neglected Tropical Diseases Escherichia Gastroenterology and Hepatology Biology Research and Analysis Methods Cell Line Bacterial genetics Microbiology 03 medical and health sciences Genetics medicine Animals Humans Enteropathogenic Escherichia coli Adhesins Bacterial Escherichia coli lcsh:R Biology and Life Sciences Tropical Diseases biology.organism_classification Rats Gastrointestinal Tract Bacterial adhesin Biological Tissue Enterocytes 030104 developmental biology Mutation Electrical Resistance lcsh:Q Caco-2 Cells Digestive System Developmental Biology |
Zdroj: | Repositório Institucional da UNIFESP Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP Scopus Repositório Institucional da UNESP Universidade Estadual Paulista (UNESP) instacron:UNESP PLoS ONE, Vol 12, Iss 2, p e0171385 (2017) PLoS ONE |
Popis: | Made available in DSpace on 2018-12-11T17:09:50Z (GMT). No. of bitstreams: 0 Previous issue date: 2017-02-01 Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) 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. Departamento de Microbiologia Imunologia E Parasitologia Universidade Federal de São Paulo Escola Paulista de Medicina (UNIFESP-EPM) Departamento de Microbiologia E Imunologia Instituto de Biociência Universidade Estadual Paulista Júlio de Mesquita Filho (UNESP) Departamento de Cirurgia Universidade Federal de São Paulo Escola Paulista de Medicina (UNIFESP-EPM) Laboratório de Biologia Celular Instituto Butantan Department of Microbiology and Biochemistry University of Texas Southwestern Medical Center Departamento de Microbiologia E Imunologia Instituto de Biociência Universidade Estadual Paulista Júlio de Mesquita Filho (UNESP) CAPES: AUX-PE-PNPD 2350/2011 |
Databáze: | OpenAIRE |
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