Renal damage and death in weaned mice after oral infection with Shiga toxin 2-producing Escherichia coli strains

Author:

Brando R J F1,Miliwebsky E2,Bentancor L1,Deza N2,Baschkier A2,Ramos M V1,Fernández G C13,Meiss R4,Rivas M2,Palermo M S13

Affiliation:

1. División Inmunología, Instituto de Investigationes Hematológicas, Academia Nacional de Medicina

2. Servicio Fisiopatogenia, Instituto Nacional de Enfermedades Infecciosas-ANLIS ‘Dr Carlos G. Malbrán’

3. Instituto de Leucemia Experimental (CONICET)

4. Departamento de Patología, Centro de Estudios Oncológicos, Academia Nacional de Medicina, Buenos Aires, Argentina

Abstract

Summary 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.

Publisher

Oxford University Press (OUP)

Subject

Immunology,Immunology and Allergy

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