Colonic microbiota alters host susceptibility to infectious colitis by modulating inflammation, redox status, and ion transporter gene expression

被引:116
作者
Ghosh, S.
Dai, C.
Brown, K.
Rajendiran, E.
Makarenko, S.
Baker, J.
Ma, C. [2 ]
Halder, S.
Montero, M. [2 ]
Ionescu, V. A.
Klegeris, A.
Vallance, B. A. [2 ]
Gibson, D. L. [1 ]
机构
[1] Univ British Columbia Okanagan, Irving K Barber Sch Arts & Sci, Dept Biol, Kelowna, BC V1V 1V7, Canada
[2] Univ British Columbia, Div Gastroenterol, BC Childrens Hosp, Vancouver, BC V5Z 1M9, Canada
来源
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY | 2011年 / 301卷 / 01期
基金
加拿大自然科学与工程研究理事会;
关键词
intestinal microbiota; Citrobacter rodentium-induced colitis; colonic inflammation; colonic oxidative stress; inflammatory bowel disease; ENTEROPATHOGENIC ESCHERICHIA-COLI; EFFACING BACTERIAL PATHOGEN; RODENTIUM-INDUCED COLITIS; CITROBACTER-RODENTIUM; ULCERATIVE-COLITIS; GUT MICROBIOTA; CROHNS-DISEASE; INTESTINAL MICROBIOTA; BACTEROIDES-FRAGILIS; BOWEL DISEASES;
D O I
10.1152/ajpgi.00509.2010
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Ghosh S, Dai C, Brown K, Rajendiran E, Makarenko S, Baker J, Ma C, Halder S, Montero M, Ionescu VA, Klegeris A, Vallance BA, Gibson DL. Colonic microbiota alters host susceptibility to infectious colitis by modulating inflammation, redox status, and ion transporter gene expression. Am J Physiol Gastrointest Liver Physiol 301: G39-G49, 2011. First published March 31, 2011; doi:10.1152/ajpgi.00509.2010.-Individuals vary in their resistance to enteric infections. The role of the intestinal microbiota in altering susceptibility to enteric infection is relatively unknown. Previous studies have identified that C3H/HeOuJ mice suffer 100% mortality during Citrobacter rodentium-induced colitis, whereas C57BL/6 mice recover from infection. The basis for their differences in susceptibility is unclear and has been mainly attributed to differences in host genetics. This study investigated the role of the intestinal microbiota in altering susceptibility to C. rodentium-induced colitis. When the feces of C57BL/6 mice were gavaged into antibiotic treated C3H/HeOuJ mice, the C57BL/6 microflora led to a complete reversal in mortality patterns where 100% of the C3H/HeOuJ mice survived infection. This protection corresponded with reduced colonic pathology and less systemic pathogen load and was associated with increased inflammatory and redox responses with reduced epithelial cell death. C3H/HeOuJ mice are normally susceptible to infection-induced dehydration due to defective expression of colonic ion transporters such as Dra, CA IV, and CA I; expression of these genes was normalized when C3H/HeOuJ mice were colonized with the C57BL/6 microflora. Together, these data reveal that the colonic microbiota play a critical role in protecting against intestinal infection by inducing proinflammatory and prooxidant responses that control pathogen load as well as ion transporter gene expression previously shown to prevent fatal dehydration. Protection of mice from lethal colitis was associated with higher levels of bacteria from Bacteroidetes. This study reveals that the microbiota is sufficient to overcome inherent genetic susceptibility patterns in C3H/HeOuJ mice that cause mortality during C. rodentium infection.
引用
收藏
页码:G39 / G49
页数:11
相关论文
共 52 条
[1]   Terminal restriction fragment length polymorphism analysis of the diversity of fecal microbiota in patients with ulcerative colitis [J].
Andoh, Akira ;
Sakata, Shinji ;
Koizumi, Yuhsuke ;
Mitsuyama, Keiichi ;
Fujiyoma, Yoshihide ;
Benno, Yoshimi .
INFLAMMATORY BOWEL DISEASES, 2007, 13 (08) :955-962
[2]  
[Anonymous], 2010, WORLD HLTH STAT 2010
[3]   IL-22 mediates mucosal host defense against Gram-negative bacterial pneumonia [J].
Aujla, Shean J. ;
Chan, Yvonne R. ;
Zheng, Mingquan ;
Fei, Mingjian ;
Askew, David J. ;
Pociask, Derek A. ;
Reinhart, Todd A. ;
McAllister, Florencia ;
Edeal, Jennifer ;
Gaus, Kristi ;
Husain, Shahid ;
Kreindler, James L. ;
Dubin, Patricia J. ;
Pilewski, Joseph M. ;
Myerburg, Mike M. ;
Mason, Carol A. ;
Iwakura, Yoichiro ;
Kolls, Jay K. .
NATURE MEDICINE, 2008, 14 (03) :275-281
[4]   Pretreatment of mice with streptomycin provides a Salmonella enterica serovar typhimurium colitis model that allows analysis of both pathogen and host [J].
Barthel, M ;
Hapfelmeier, S ;
Quintanilla-Martínez, L ;
Kremer, M ;
Rohde, M ;
Hogardt, M ;
Pfeffer, K ;
Rüssmann, H ;
Hardt, WD .
INFECTION AND IMMUNITY, 2003, 71 (05) :2839-2858
[5]   Modulation of intestinal goblet cell function during infection by an attaching and effacing bacterial pathogen [J].
Bergstrom, Kirk S. B. ;
Guttman, Julian A. ;
Rumi, Mohammad ;
Ma, Caixia ;
Bouzari, Saied ;
Khan, Mohammed A. ;
Gibson, Deanna L. ;
Vogl, A. Wayne ;
Vallance, Bruce A. .
INFECTION AND IMMUNITY, 2008, 76 (02) :796-811
[6]   Decreased Expression of Colonic Slc26a3 and Carbonic Anhydrase IV as a Cause of Fatal Infectious Diarrhea in Mice [J].
Borenshtein, Diana ;
Schlieper, Katherine A. ;
Rickman, Barry H. ;
Chapman, Jeannie M. ;
Schweinfest, Clifford W. ;
Fox, James G. ;
Schauer, David B. .
INFECTION AND IMMUNITY, 2009, 77 (09) :3639-3650
[7]   Effects of gut microbiota on obesity and atherosclerosis via modulation of inflammation and lipid metabolism [J].
Caesar, R. ;
Fak, F. ;
Backhed, F. .
JOURNAL OF INTERNAL MEDICINE, 2010, 268 (04) :320-328
[8]   Role of Intestinal Bacteria in Gliadin-Induced Changes in Intestinal Mucosa: Study in Germ-Free Rats [J].
Cinova, Jana ;
De Palma, Giada ;
Stepankova, Renata ;
Kofronova, Olga ;
Kverka, Miloslav ;
Sanz, Yolanda ;
Tuckova, Ludmila .
PLOS ONE, 2011, 6 (01)
[9]   Host/pathogen interactions at mucosal surfaces: Immune consequences [J].
Clare, S ;
Huett, A ;
Dougan, G .
RESEARCH IN MICROBIOLOGY, 2002, 153 (07) :455-459
[10]   Diversity of the human intestinal microbial flora [J].
Eckburg, PB ;
Bik, EM ;
Bernstein, CN ;
Purdom, E ;
Dethlefsen, L ;
Sargent, M ;
Gill, SR ;
Nelson, KE ;
Relman, DA .
SCIENCE, 2005, 308 (5728) :1635-1638