1993
DOI: 10.1016/0016-5085(93)90415-9
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The effect of enterohemorrhagic Escherichia coli 0157:H7 on intestinal structure and solute transport in rabbits

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Cited by 55 publications
(44 citation statements)
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“…A number of experimental animal models have been proposed to study the pathogenicity of STEC (63), including gnotobiotic mice (17,18,64), streptomycin-treated mice (15,27,32,61,62), gnotobiotic piglets (14,59), newborn chickens (5), and infant rabbits (26,36,44,50). While mouse models have been used most frequently to date, most are not appropriate because high doses of inoculum, more than 10 7 CFU/body, are usually required for establishment of STEC infection, and often mice do not develop diarrhea even when they are inoculated with such high doses of STEC (21,23).…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…A number of experimental animal models have been proposed to study the pathogenicity of STEC (63), including gnotobiotic mice (17,18,64), streptomycin-treated mice (15,27,32,61,62), gnotobiotic piglets (14,59), newborn chickens (5), and infant rabbits (26,36,44,50). While mouse models have been used most frequently to date, most are not appropriate because high doses of inoculum, more than 10 7 CFU/body, are usually required for establishment of STEC infection, and often mice do not develop diarrhea even when they are inoculated with such high doses of STEC (21,23).…”
Section: Discussionmentioning
confidence: 99%
“…While mouse models have been used most frequently to date, most are not appropriate because high doses of inoculum, more than 10 7 CFU/body, are usually required for establishment of STEC infection, and often mice do not develop diarrhea even when they are inoculated with such high doses of STEC (21,23). On the contrary, the rabbit model has the major advantages of the reproducibility of diarrhea and susceptibility to STEC infection and Stx toxicity (7,26,36,44,50,55). In this study, we used the infant rabbit model with administration of a lower number of bacteria (ϳ10 3 CFU/body) than reported previously (36,44,50).…”
Section: Discussionmentioning
confidence: 99%
“…to result in less severe lesions in colonic epithelial cells than the E. coli containing the both Stx genes and a LEE region (15), thus suggesting that the LEE-induced A/E phenomenon and the following internalization play a crucial role in the pathogenesis of STEC infection.…”
mentioning
confidence: 99%
“…Subsequent studies identified the colon as the principal site of EHEC-mediated disease, where histological abnormalities, including edema, hemorrhage, the presence of an inflammatory infiltrate, and mucosal epithelial apoptosis, were observed (66,67). In these young animals, the development of diarrhea appears to be driven by inflammation-mediated changes in colonic ion transport resulting in decreased Na absorption and increased Cl secretion (68,69). Unlike humans, suckling rabbits do not develop signs of renal disease; however, the reproduction of diarrhea and colonic inflammation, two key features of EHEC infection in humans, indicates that they may be a useful model for studying the intestinal manifestations of the disease.…”
Section: Rabbitsmentioning
confidence: 99%