1994
DOI: 10.1016/0016-5085(94)90587-8
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Role of shiga-like toxin I in bacterial enteritis: Comparison between isogenic Escherichia coli strains induced in rabbits

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Cited by 73 publications
(56 citation statements)
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“…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%
“…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%
“…Our results are compatible with previous studies cited above showing that Stx2 is necessary for disease in orally infected mice, but studies performed with other models suggest a role for Stx1 in disease. For example, Sjogren et al (47) observed enhanced severity of enteric disease in rabbits infected with RDEC that was engineered to express Stx1. Also, direct injection studies with mice have shown that parenteral Stx1 alone, as well as Stx2, causes renal disease (20,51).…”
Section: %)mentioning
confidence: 99%
“…Evidence provided by Rashid et al (2006) indicated that Shiga toxins are equally expressed in EHEC O157:H7-challenged cattle and humans suggesting that these toxins could have an impact on intestinal mucosa from cattle. Shiga toxins and other cytotoxins are toxic to epithelial cell lines, primary cultures of animal cells in vitro and intestinal organ cultures (Konowalchuk et al 1977;Sjogren et al 1994;Bauer and Welch 1996;Valdivieso-Garcia et al 1996;Schuller et al 2004;Aldick et al 2007). These toxins can also affect gene expression in lymphocytes (Ferens and Hovde 2000;Menge et al 2004), fibroblasts (Ferens and Hovde 2007) and epithelial cell lines (Robinson et al 2006).…”
Section: Ivoc Adherence Assaymentioning
confidence: 99%