Use este identificador para citar ou linkar para este item: http://sgc.anlis.gob.ar/handle/123456789/1857
Título: Renal damage and death in weaned mice after oral infection with Shiga toxin 2-producing Escherichia coli strains
Autor(es): Brando, R J F 
Miliwebsky, Elizabeth 
Bentancor, L 
Deza, N. 
Baschkier, Ariela 
Ramos, Marina A. 
Fernandez, G. C. 
Meiss, R 
Rivas, Marta 
Palermo, M. 
Palavras-chave: Escherichia coli;Toxina Shiga
Data do documento: Ago-2008
Editora: Wiley
Jornal: Clinical and experimental immunology 
Resumo: 
Enterohaemorrhagic Escherichia coli (EHEC) O157:H7 infections are considered a public health problem in both developed and developing countries because of their increasing incidence and the severity of clinical presentation. Approximately 10% of infected patients develop complications such as haemolytic uraemic syndrome (HUS) characterized by acute renal failure, thrombocytopenia and haemolytic anaemia. The precise sequence of events leading to HUS is still understood incompletely. Because of the lack of a reproducible small animal model for EHEC infections, in vivo studies examining EHEC-host early interactions are limited and insufficient. The aim of this study was to characterize the weaned BALB/c mouse as a model of E. coli O157:H7 infection. In this paper we report that human Shiga toxin 2 (Stx2)-producing EHEC strains can adhere to the intestinal epithelium of weaned BALB/c mice, and produce local damage which leads to systemic disease and death in a percentage of infected mice. The lethality of the EHEC strain is closely age-dependent, and is related to the bacterial ability to colonize intestine and to produce Stx2. It can be concluded that the weaned BALB/c mouse can be used as a small animal model to study host early responses, and the role of bacterial pathogenic factors in the induction of systemic disease, thus providing a useful tool for the evaluation of therapeutic or vaccine approaches.
Descrição: 
Fil: Brando, R J F. División Inmunología, Instituto de Investigationes Hematológicas, Academia Nacional de Medicina; Argentina.

Fil: Miliwebsky, Elizabeth. ANLIS Dr.C.G.Malbrán. Instituto Nacional de Enfermedades Infecciosas. Departamento de Bacteriología. Servicio Fisiopatogenia; Argentina.

Fil: Bentancor, L. División Inmunología, Instituto de Investigationes Hematológicas, Academia Nacional de Medicina; Argentina.

Fil: Deza, N. ANLIS Dr.C.G.Malbrán. Instituto Nacional de Enfermedades Infecciosas. Departamento de Bacteriología. Servicio Fisiopatogenia; Argentina.

Fil: Baschkier, Ariela. ANLIS Dr.C.G.Malbrán. Instituto Nacional de Enfermedades Infecciosas. Departamento de Bacteriología. Servicio Fisiopatogenia; Argentina.

Fil: Ramos, Marina A. División Inmunología, Instituto de Investigationes Hematológicas, Academia Nacional de Medicina; Argentina.

Fil: Fernández, G. C. ANLIS Dr.C.G.Malbrán. Instituto Nacional de Enfermedades Infecciosas. Departamento de Bacteriología. Servicio Fisiopatogenia; Argentina.

Fil: Meiss, R. Departamento de Patología, Centro de Estudios Oncológicos, Academia Nacional de Medicina; Argentina.

Fil: Rivas, Marta. ANLIS Dr.C.G.Malbrán. Instituto Nacional de Enfermedades Infecciosas. Departamento de Bacteriología. Servicio Fisiopatogenia; Argentina.

Fil: Palermo, M. División Inmunología, Instituto de Investigationes Hematológicas, Academia Nacional de Medicina; Argentina.
URI: http://sgc.anlis.gob.ar/handle/123456789/1857
ISSN: 1365-2249
DOI: 10.1111/j.1365-2249.2008.03698.x
Direitos: Open Access
Creative Commons Attribution 4.0 International License
Aparece nas Coleções:Publicaciones INEI

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