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Beta toxin is essential for the intestinal virulence of Clostridium perfringens type C disease isolate CN3685 in a rabbit ileal loop model.

Beta toxin is essential for the intestinal virulence of Clostridium perfringens type C disease isolate CN3685 in a rabbit ileal loop model. Research Abstract Details 

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  • Beta toxin is essential for the intestinal virulence of Clostridium perfringens type C disease isolate CN3685 in a rabbit ileal loop model. Abstract Text:

    sameera sayeedSameera Sayeed,francisco a uzalFrancisco A Uzal,derek j fisherDerek J Fisher,juliann saputoJuliann Saputo,jorge e vidalJorge E Vidal,yue chenYue Chen,phalguni guptaPhalguni Gupta,julian i roodJulian I Rood,bruce a mcclaneBruce A McClane,

    Clostridium perfringens type C isolates, which cause enteritis necroticans in humans and enteritis and enterotoxaemias of domestic animals, typically produce (at minimum) beta toxin (CPB), alpha toxin (CPA) and perfringolysin O (PFO) during log-phase growth. To assist development of improved vaccines and therapeutics, we evaluated the contribution of these three toxins to the intestinal virulence of type C disease isolate CN3685. Similar to natural type C infection, log-phase vegetative cultures of wild-type CN3685 caused haemorrhagic necrotizing enteritis in rabbit ileal loops. When isogenic toxin null mutants were prepared using TargeTron((R)) technology, even a double cpa/pfoA null mutant of CN3685 remained virulent in ileal loops. However, two independent cpb null mutants were completely attenuated for virulence in this animal model. Complementation of a cpb mutant restored its CPB production and intestinal virulence. Additionally, pre-incubation of wild-type CN3685 with a CPB-neutralizing monoclonal antibody rendered the strain avirulent for causing intestinal pathology. Finally, highly purified CPB reproduced the intestinal damage of wild-type CN3685 and that damage was prevented by pre-incubating purified CPB with a CPB monoclonal antibody. These results indicate that CPB is both required and sufficient for CN3685-induced enteric pathology, supporting a key role for this toxin in type C intestinal pathogenesis.

    Beta toxin is essential for the intestinal virulence of Clostridium perfringens type C disease isolate CN3685 in a rabbit ileal loop model. Publishing Authors By Initials

    s sayeedS Sayeed,fa uzalFA Uzal,dj fisherDJ Fisher,j saputoJ Saputo,je vidalJE Vidal,y chenY Chen,p guptaP Gupta,ji roodJI Rood,ba mcclaneBA McClane,

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    Beta toxin is essential for the intestinal virulence of Clostridium perfringens type C disease isolate CN3685 in a rabbit ileal loop model. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Molecular microbiology

    VOLUME: 67

    Page Numbers: 15-30

    Journal Abbreviation: Mol. Microbiol.

    ISSN: 0950-382X

    DAY: 14

    MONTH: Jan

    YEAR: 2008

    Beta toxin is essential for the intestinal virulence of Clostridium perfringens type C disease isolate CN3685 in a rabbit ileal loop model. Information

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    LANGUAGE: eng

    NlmUniqueID: 8712028

    Beta toxin is essential for the intestinal virulence of Clostridium perfringens type C disease isolate CN3685 in a rabbit ileal loop model. Keywords Mesh Terms:

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    Grant and Affiliation Information for Beta toxin is essential for the intestinal virulence of Clostridium perfringens type C disease isolate CN3685 in a rabbit ileal loop model.

    AFFILIATION: Department of Molecular Genetics and Biochemistry, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.

    Country: England

    England Research PublicationEngland Research Publication

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    MEDLINETA: Mol Microbiol

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