Citrobacter rodentium infection causes iNOS-independent intestinal epithelial dysfunction in mice

被引:10
作者
Skinn, Andrew C.
Vergnolle, Nathalie
Zamuner, Stella R.
Wallace, John L.
Cellars, Laurie
MacNaughton, Wallace K.
Sherman, Philip M.
机构
[1] Univ Calgary, Mucosal Inflammat Res Grp, Calgary, AB T2N 4N1, Canada
[2] Univ Calgary, Dept Physiol & Biophys, Calgary, AB T2N 4N1, Canada
[3] Univ Toronto, Hosp Sick Children, Toronto, ON M5G 1X8, Canada
关键词
epithelium; infection; ion transport; nitric oxide; inflammation; colon;
D O I
10.1139/Y06-086
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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 C57B1/6 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.
引用
收藏
页码:1301 / 1312
页数:12
相关论文
共 33 条
[1]   Prolonged colonic epithelial hyporesponsiveness after colitis: role of inducible nitric oxide synthase [J].
Asfaha, S ;
Bell, CJ ;
Wallace, JL ;
MacNaughton, WK .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1999, 276 (03) :G703-G710
[2]   Persistent epithelial dysfunction and bacterial translocation after resolution of intestinal inflammation [J].
Asfaha, S ;
MacNaughton, WK ;
Appleyard, CB ;
Chadee, K ;
Wallace, JL .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2001, 281 (03) :G635-G644
[3]   TRANSMISSIBLE MURINE COLONIC HYPERPLASIA [J].
BARTHOLD, SW ;
COLEMAN, GL ;
JACOBY, RO ;
LIVSTONE, EM ;
JONAS, AM .
VETERINARY PATHOLOGY, 1978, 15 (02) :223-236
[4]   Intestinal epithelial responses to enteric pathogens: effects on the tight junction barrier, ion transport, and inflammation [J].
Berkes, J ;
Viswanathan, VK ;
Savkovic, SD ;
Hecht, G .
GUT, 2003, 52 (03) :439-451
[5]   CD4+-T-cell effector functions and costimulatory requirements essential for surviving mucosal infection with Citrobacter rodentium [J].
Bry, L ;
Brigl, M ;
Brenner, MB .
INFECTION AND IMMUNITY, 2006, 74 (01) :673-681
[6]   MUCOSAL RESPONSES EVOKED BY STIMULATION OF GANGLION-CELL SOMAS IN THE SUBMUCOSAL PLEXUS OF THE GUINEA-PIG ILEUM [J].
CAREY, HV ;
COOKE, HJ ;
ZAFIROVA, M .
JOURNAL OF PHYSIOLOGY-LONDON, 1985, 364 (JUL) :69-+
[7]   Induction of intestinal inflammation in mouse by activation of proteinase-activated receptor-2 [J].
Cenac, N ;
Coelho, AM ;
Nguyen, C ;
Compton, S ;
Andrade-Gordon, P ;
MacNaughton, WK ;
Wallace, JL ;
Hollenberg, MD ;
Bunnett, NW ;
Garcia-Villar, R ;
Bueno, L ;
Vergnolle, N .
AMERICAN JOURNAL OF PATHOLOGY, 2002, 161 (05) :1903-1915
[8]   NOX, a novel nitric oxide scavenger, reduces bacterial translocation in rats after endotoxin challenge [J].
Dickinson, E ;
Tuncer, R ;
Nadler, E ;
Boyle, P ;
Alber, S ;
Watkins, S ;
Ford, H .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1999, 277 (06) :G1281-G1287
[9]   Gene disruption and immunity in experimental colitis [J].
Elson, CO ;
Konrad, A ;
Cong, YZ ;
Weaver, CT .
INFLAMMATORY BOWEL DISEASES, 2004, 10 :S25-S28
[10]   New developments in experimental models of inflammatory bowel disease [J].
Elson, CO ;
Cong, YZ ;
Lorenz, R ;
Weaver, CT .
CURRENT OPINION IN GASTROENTEROLOGY, 2004, 20 (04) :360-367