• Media type: E-Article
  • Title: Citrobacter rodentiuminfection causes iNOS-independent intestinal epithelial dysfunction in mice
  • Contributor: Skinn, Andrew C.; Vergnolle, Nathalie; Zamuner, Stella R.; Wallace, John L.; Cellars, Laurie; MacNaughton, Wallace K.; Sherman, Philip M.
  • Published: Canadian Science Publishing, 2006
  • Published in: Canadian Journal of Physiology and Pharmacology, 84 (2006) 12, Seite 1301-1312
  • Language: English
  • DOI: 10.1139/y06-086
  • ISSN: 0008-4212; 1205-7541
  • Keywords: Physiology (medical) ; Pharmacology ; General Medicine ; Physiology
  • Origination:
  • Footnote:
  • Description: Attaching-effacing bacteria are major causes of infectious diarrhea in humans worldwide. Citrobacter rodentium is an attaching-effacing enteric pathogen that causes transmissible murine colonic mucosal hyperplasia. We characterized colonic inflammation and ion transport at 3, 7, 10, 30, and 60 d after infection of C57Bl/6 mice with C. rodentium. Macroscopic damage score was significantly increased 7 and 10 d after infection. Colonic wall thickness was increased at 7, 10, 30, and 60 d. Myeloperoxidase (MPO) activity was significantly increased at 3, 7, and 10 d and returned to control levels by days 30 and 60. The expressions of inducible nitric oxide synthase and cyclooxygenase-2 were increased by C. rodentium infection. Significant reductions in the epithelial secretory response to carbachol, but not to electrical field stimulation or forskolin, were observed at 3 and 10 d of infection. Translocation of enteric bacteria into the mesenteric lymph nodes was observed 10 d following infection. There was no difference in response to infection between animals deficient in inducible nitric oxide synthase and wild-type controls. The COX-2 inhibitor rofecoxib caused decreased wall thickness and MPO activity at day 10. However, COX-2 inhibition did not alter infection-induced changes in ion transport. Citrobacter rodentium infection causes colonic inflammation, mucosal hyperplasia, and nitric-oxide-independent epithelial dysfunction in association with increased permeability to luminal bacteria.