Please use this identifier to cite or link to this item: http://repositorio.unifesp.br/handle/11600/31678
Title: Invasiveness as a putative additional virulence mechanism of some atypical Enteropathogenic Escherichia coli strains with different uncommon intimin types
Authors: Yamamoto, Denise [UNIFESP]
Hernandes, Rodrigo T. [UNIFESP]
Blanco, Miguel
Greune, Lilo
Schmidt, M. Alexander
Carneiro, Sylvia M.
Dahbi, Ghizlane
Blanco, Jesus E.
Mora, Azucena
Blanco, Jorge
Gomes, Tania Aparecida Tardelli [UNIFESP]
Universidade Federal de São Paulo (UNIFESP)
Univ Munster
Univ Santiago de Compostela
Inst Butantan
Issue Date: 21-Jul-2009
Publisher: Biomed Central Ltd
Citation: Bmc Microbiology. London: Biomed Central Ltd, v. 9, 10 p., 2009.
Abstract: Background: Enteropathogenic Escherichia coli (EPEC) produce attaching/effacing (A/E) lesions on eukaryotic cells mediated by the outer membrane adhesin intimin. EPEC are sub-grouped 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 sub-type omicron. in this study, we evaluated whether aEPEC strains expressing other intimin sub-types are also invasive using the quantitative gentamicin protection assay. We also evaluated whether aEPEC invade differentiated intestinal T84 cells.Results: 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 cell-associated 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). Invasiveness 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, disruption of tight junctions enhanced its invasion efficiency in T84 cells, suggesting preferential invasion via a non-differentiated surface.Conclusion: Some aEPEC strains may invade intestinal cells in vitro with varying efficiencies and independently of the intimin sub-type.
URI: http://repositorio.unifesp.br/handle/11600/31678
ISSN: 1471-2180
Other Identifiers: http://dx.doi.org/10.1186/1471-2180-9-146
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