Ocorrência e caracterização de eventos de invasão de linhagens celulares cultivadas in vitro por amostras de Escherichia coli enteropatogênica (EPEC) atípica

Enteropathogenic Escherichia coli (EPEC) produce attaching/effacing (A/E) lesions on eukaryotic cells mediated by the outer membrane adhesin Intimin. EPEC are subgrouped into typical (tEPEC) and atypical (aEPEC). We have recently demonstrated that aEPEC strain 1551-2 (serotype O non-typable, non-mot...

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Bibliographic Details
Author: Yamamoto, Denise [UNIFESP]
Format: doctoral thesis
Status:Published version
Publication Date:2009
Country:Brasil
Institution:Universidade Federal de São Paulo (UNIFESP)
Repository:Repositório Institucional da UNIFESP
Language:Portuguese
OAI Identifier:oai:repositorio.unifesp.br:11600/9879
Online Access:http://repositorio.unifesp.br/handle/11600/9879
Access Level:Open access
Keyword:Escherichia coli
EPEC atípica
Intimina
Invasão
Diarréia
Escherichia coli Enteropatogênica
Enteropathogenic escherichia coli
Invasion
Diarrhea
Description
Summary:Enteropathogenic Escherichia coli (EPEC) produce attaching/effacing (A/E) lesions on eukaryotic cells mediated by the outer membrane adhesin Intimin. EPEC are subgrouped into typical (tEPEC) and atypical (aEPEC). We have recently demonstrated that aEPEC strain 1551-2 (serotype O non-typable, non-motile) invades HeLa cells by a process dependent on the expression of intimin subtype omicron. In this study, we evaluated whether aEPEC strains expressing other intimin subtypes are also invasive using the quantitative gentamicin protection assay. We also evaluated whether aEPEC invade intestinal differentiated T84 cells. Five of six strains invaded HeLa and T84 cells in a range of 13.3%-20.9% and 5.8%-17.8%, respectively, of the total cellassociated bacteria. The strains studied were significantly more invasive than prototype tEPEC strain E2348/69 (1.4% and 0.5% in HeLa and T84 cells, respectively). aEPEC strain 1551-2 was also tested in differentiated Caco-2 cells, resulting in an invasion index similar to that obtained in T84 cells (7.5%±1.7%). This strain was also significantly more invasive than prototype tEPEC strain E2348/69 (1.8%±0.6%). Invasiveness of T84 cells was confirmed by transmission electron microscopy. We also showed that invasion of HeLa cells by aEPEC 1551-2 depended on actin filaments, but not on microtubules. In addition, infection of non-differentiated monolayers and disruption of tight junctions enhanced its invasion efficiency in T84 cells, suggesting preferential invasion via a non-differentiated surface. In summary, aEPEC strains may invade intestinal cells in vitro with varying efficiencies and independently of the intimin subtype.