4.4 Article

Differential Outcome between BALB/c and C57BL/6 Mice after Escherichia coli O157:H7 Infection Is Associated with a Dissimilar Tolerance Mechanism

期刊

INFECTION AND IMMUNITY
卷 89, 期 5, 页码 -

出版社

AMER SOC MICROBIOLOGY
DOI: 10.1128/IAI.00031-21

关键词

EHEC; intestinal infection; mouse model; defense mechanisms; antibodies; Shiga toxins

资金

  1. Agencia Nacional de Promocion Cientifica y Tecnologica of Argentina [PICT 2016-0278]

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Despite similar susceptibility to Shiga toxin and comparable intestinal bacterial burden between C57BL/6 and BALB/c mice, C57BL/6 mice exhibited more severe intestinal damage and impaired renal function leading to increased mortality, while the higher survival rate in BALB/c mice was associated with an early specific antibody response as part of a tolerance mechanism.
Enterohemorrhagic Escherichia coli (EHEC) infections can result in a wide range of clinical presentations despite that EHEC strains belong to the O157:H7 serotype, one of the most pathogenic forms. Although pathogen virulence influences disease outcome, we emphasize the concept of host-pathogen interactions, which involve resistance or tolerance mechanisms in the host that determine total host fitness and bacterial virulence. Taking advantage of the genetic differences between mouse strains, we analyzed the clinical progression in C57B1/6 and BALB/c weaned mice infected with an E. coli O157:H7 strain. We carefully analyzed colonization with several bacterial doses, clinical parameters, intestinal histology, and the integrity of the intestinal barrier, as well as local and systemic levels of antibodies to pathogenic factors. We demonstrated that although both strains had comparable susceptibility to Shiga toxin (Stx) and the intestinal bacterial burden was similar, C57BL/6 showed increased intestinal damage, alteration of the integrity of the intestinal barrier, and impaired renal function that resulted in increased mortality. The increased survival rate in the BALB/c strain was associated with an early specific antibody response as part of a tolerance mechanism.

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