Modulation of inducible nitric oxide synthase expression by the attaching and effacing bacterial pathogen Citrobacter rodentium in infected mice

被引:82
作者
Vallance, BA
Deng, WY
De Grado, M
Chan, C
Jacobson, K
Finlay, BB
机构
[1] Univ British Columbia, Biotechnol Lab, Vancouver, BC V6T 1Z3, Canada
[2] British Columbia Childrens Hosp, Div Gastroenterol, Dept Pediat, Vancouver, BC V6T 1Z3, Canada
关键词
D O I
10.1128/IAI.70.11.6424-6435.2002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Citrobacter rodentium belongs to the attaching and effacing family of enteric bacterial pathogens that includes both enteropathogenic and enterohemorrhagic Escherichia coli. These bacteria infect their hosts by colonizing the intestinal mucosal surface and intimately attaching to underlying epithelial cells. The abilities of these pathogens to exploit the cytoskeleton and signaling pathways of host cells are well documented, but their interactions with the host's antimicrobial defenses, such as inducible nitric oxide synthase (iNOS), are poorly understood. To address this issue, we infected mice with C. rodentium and found that iNOS mRNA expression in the colon significantly increased during infection. Immunostaining identified epithelial cells as the major source for immunoreactive iNOS. Finding that nitric oxide (NO) donors were bacteriostatic for C. rodentium in vitro, we examined whether iNOS expression contributed to host defense by infecting iNOS-deficient mice. Loss of iNOS expression caused a small but significant delay in bacterial clearance without affecting tissue pathology. Finally, immunofluorescence staining was used to determine if iNOS expression was localized to infected cells by staining for the C rodentium virulence factor, translocated intimin receptor (Tir), as well as iNOS. Interestingly, while more than 85% of uninfected epithelial cells expressed iNOS, fewer than 15% of infected (Tir-positive) cells expressed detectable iNOS. These results demonstrate that both iNOS and intestinal epithelial cells play an active role in host defense during C. rodentium infection. However, the selective expression of iNOS by uninfected but not infected cells suggests that this pathogen has developed mechanisms to locally limit its exposure to host-derived NO.
引用
收藏
页码:6424 / 6435
页数:12
相关论文
共 65 条
[41]  
Nataro JP, 1998, CLIN MICROBIOL REV, V11, P142
[42]   Reactive oxygen and nitrogen intermediates in the relationship between mammalian hosts and microbial pathogens [J].
Nathan, C ;
Shiloh, MU .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (16) :8841-8848
[43]   PROTRACTED DIARRHEA - THE IMPORTANCE OF THE ENTEROPATHOGENIC-E-COLI (EPEC) STRAINS AND SALMONELLA IN ITS GENESIS [J].
NETO, UF ;
FERREIRA, VD ;
PATRICIO, FRS ;
MOSTACO, VL ;
TRABULSI, LR .
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION, 1989, 8 (02) :207-211
[44]   Citrobacter rodentium espB is necessary for signal transduction and for infection of laboratory mice [J].
Newman, JV ;
Zabel, BA ;
Jha, SS ;
Schauer, DB .
INFECTION AND IMMUNITY, 1999, 67 (11) :6019-6025
[45]   Colonic production of nitric oxide gas in ulcerative colitis, collagenous colitis and uninflamed bowel [J].
Perner, A ;
Nordgaard, I ;
Matzen, P ;
Rask-Madsen, J .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 2002, 37 (02) :183-188
[46]  
Philpott DJ, 2001, CURR OPIN IMMUNOL, V13, P410
[47]   ADHERENCE CHARACTERISTICS OF ATTACHING AND EFFACING STRAINS OF ESCHERICHIA-COLI FROM RABBITS [J].
ROBINSBROWNE, RM ;
TOKHI, AM ;
ADAMS, LM ;
BENNETTWOOD, V ;
MOISIDIS, AV ;
KREJANY, EO ;
OGORMAN, LE .
INFECTION AND IMMUNITY, 1994, 62 (05) :1584-1592
[48]   Bacterial induction of inducible nitric oxide synthase in cultured human intestinal epithelial cells [J].
Salzman, AL ;
Eaves-Pyles, T ;
Linn, SC ;
Denenberg, AG ;
Szabo, C .
GASTROENTEROLOGY, 1998, 114 (01) :93-102
[49]   Attachment of a noninvasive enteric pathogen, enteropathogenic Escherichia coli, to cultured human intestinal epithelial monolayers induces transmigration of neutrophils [J].
Savkovic, SD ;
Koutsouris, A ;
Hecht, G .
INFECTION AND IMMUNITY, 1996, 64 (11) :4480-4487
[50]   EPEC-activated ERK1/2 participate in inflammatory response but not tight junction barrier disruption [J].
Savkovic, SD ;
Ramaswamy, A ;
Koutsouris, A ;
Hecht, G .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2001, 281 (04) :G890-G898