Artículo
Disassembly of F-Actin Cytoskeleton after Interaction of Bacillus cereus with Fully Differentiated Human Intestinal Caco-2 Cells
Minnaard, Jessica
; Lievin Le Moal, Vanessa; Coconnier, Marie Helene; Servin, Alain L.; Perez, Pablo Fernando
Fecha de publicación:
06/2004
Editorial:
American Society for Microbiology
Revista:
Infection and Immunity
ISSN:
0019-9567
e-ISSN:
1098-5522
Idioma:
Inglés
Tipo de recurso:
Artículo publicado
Clasificación temática:
Resumen
In the present study the role of direct procaryote-eucaryote interactions in the virulence of Bacillus cereus has been investigated. As a model of human enterocytes, differentiated Caco-2 cells were used. Infection of fully differentiated Caco-2 cells with B. cereus in exponential phase of growth, in order to minimize the concentration of spores or sporulating microorganisms, shows that a strain-dependent cytopathic effect develops. Interestingly, three hours-old cultures of some strains completely detached the cultured cells after 3 h post-infection, whereas no such effect was found with 16 h-old cultures. Infection of enterocyte-like cells with B. cereus leads to disruption of the F-actin network and necrosis. Even though, the effect of secreted factors cannot be ruled out, the direct eucaryote-procaryote interaction seems to be necessary. In addition, we observed that some B. cereus strains were able to internalize into Caco-2 cells. Our findings add a new insight on the mechanisms of virulence of B. cereus in the context of intestinal infection.
Palabras clave:
Bacillus cereus
,
Human Intestinal
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Articulos(CIDCA)
Articulos de CENTRO DE INV EN CRIOTECNOLOGIA DE ALIMENTOS (I)
Articulos de CENTRO DE INV EN CRIOTECNOLOGIA DE ALIMENTOS (I)
Citación
Minnaard, Jessica; Lievin Le Moal, Vanessa; Coconnier, Marie Helene; Servin, Alain L.; Perez, Pablo Fernando; Disassembly of F-Actin Cytoskeleton after Interaction of Bacillus cereus with Fully Differentiated Human Intestinal Caco-2 Cells; American Society for Microbiology; Infection and Immunity; 72; 6; 6-2004; 3106-3112
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