Vallance Bruce A, Deng Wanyin, De Grado Myriam, Chan Crystal, Jacobson Kevan, Finlay B Brett
Biotechnology Laboratory, University of British Columbia, Vancouver, British Columbia, Canada V6T 1Z3.
Infect Immun. 2002 Nov;70(11):6424-35. doi: 10.1128/IAI.70.11.6424-6435.2002.
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.
鼠柠檬酸杆菌属于肠道细菌病原体的紧密黏附性家族,该家族包括肠致病性大肠杆菌和肠出血性大肠杆菌。这些细菌通过定殖于肠道黏膜表面并紧密附着于下方的上皮细胞来感染宿主。这些病原体利用宿主细胞细胞骨架和信号通路的能力已有充分记载,但它们与宿主抗菌防御机制(如诱导型一氧化氮合酶(iNOS))的相互作用却知之甚少。为了解决这个问题,我们用鼠柠檬酸杆菌感染小鼠,发现感染期间结肠中iNOS mRNA表达显著增加。免疫染色确定上皮细胞是免疫反应性iNOS的主要来源。鉴于一氧化氮(NO)供体在体外对鼠柠檬酸杆菌具有抑菌作用,我们通过感染iNOS缺陷小鼠来研究iNOS表达是否有助于宿主防御。iNOS表达缺失导致细菌清除出现轻微但显著的延迟,且不影响组织病理学。最后,通过对鼠柠檬酸杆菌毒力因子转位紧密素受体(Tir)以及iNOS进行染色,利用免疫荧光染色来确定iNOS表达是否定位于感染细胞。有趣的是,虽然超过85%未感染的上皮细胞表达iNOS,但感染(Tir阳性)细胞中表达可检测到的iNOS的细胞少于15%。这些结果表明,iNOS和肠道上皮细胞在鼠柠檬酸杆菌感染期间的宿主防御中均发挥积极作用。然而,未感染而非感染细胞对iNOS的选择性表达表明,这种病原体已形成局部限制其暴露于宿主来源NO的机制。