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Enterotoxicity of a nonribosomal peptide causes antibiotic-associated colitis.


ABSTRACT: Antibiotic therapy disrupts the human intestinal microbiota. In some patients rapid overgrowth of the enteric bacterium Klebsiella oxytoca results in antibiotic-associated hemorrhagic colitis (AAHC). We isolated and identified a toxin produced by K. oxytoca as the pyrrolobenzodiazepine tilivalline and demonstrated its causative action in the pathogenesis of colitis in an animal model. Tilivalline induced apoptosis in cultured human cells in vitro and disrupted epithelial barrier function, consistent with the mucosal damage associated with colitis observed in human AAHC and the corresponding animal model. Our findings reveal the presence of pyrrolobenzodiazepines in the intestinal microbiota and provide a mechanism for colitis caused by a resident pathobiont. The data link pyrrolobenzodiazepines to human disease and identify tilivalline as a target for diagnosis and neutralizing strategies in prevention and treatment of colitis.

SUBMITTER: Schneditz G 

PROVIDER: S-EPMC4246982 | biostudies-literature | 2014 Sep

REPOSITORIES: biostudies-literature

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Enterotoxicity of a nonribosomal peptide causes antibiotic-associated colitis.

Schneditz Georg G   Rentner Jana J   Roier Sandro S   Pletz Jakob J   Herzog Kathrin A T KA   Bücker Roland R   Troeger Hanno H   Schild Stefan S   Weber Hansjörg H   Breinbauer Rolf R   Gorkiewicz Gregor G   Högenauer Christoph C   Zechner Ellen L EL  

Proceedings of the National Academy of Sciences of the United States of America 20140825 36


Antibiotic therapy disrupts the human intestinal microbiota. In some patients rapid overgrowth of the enteric bacterium Klebsiella oxytoca results in antibiotic-associated hemorrhagic colitis (AAHC). We isolated and identified a toxin produced by K. oxytoca as the pyrrolobenzodiazepine tilivalline and demonstrated its causative action in the pathogenesis of colitis in an animal model. Tilivalline induced apoptosis in cultured human cells in vitro and disrupted epithelial barrier function, consis  ...[more]

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