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Modulation of inducible nitric oxide synthase expression by the attaching and effacing bacterial pathogen citrobacter rodentium in infected mice.感染小鼠中黏附和损伤性细菌病原体鼠柠檬酸杆菌对诱导型一氧化氮合酶表达的调节
Infect Immun. 2002 Nov;70(11):6424-35. doi: 10.1128/IAI.70.11.6424-6435.2002.
2
Impaired resistance and enhanced pathology during infection with a noninvasive, attaching-effacing enteric bacterial pathogen, Citrobacter rodentium, in mice lacking IL-12 or IFN-gamma.在缺乏白细胞介素-12或干扰素-γ的小鼠中,感染非侵袭性、黏附-侵蚀性肠道细菌病原体啮齿柠檬酸杆菌期间,抵抗力受损且病理状况加重。
J Immunol. 2002 Feb 15;168(4):1804-12. doi: 10.4049/jimmunol.168.4.1804.
3
Citrobacter rodentium infection causes iNOS-independent intestinal epithelial dysfunction in mice.鼠柠檬酸杆菌感染导致小鼠出现不依赖诱导型一氧化氮合酶的肠道上皮功能障碍。
Can J Physiol Pharmacol. 2006 Dec;84(12):1301-12. doi: 10.1139/y06-086.
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Modulation of intestinal goblet cell function during infection by an attaching and effacing bacterial pathogen.在感染期间,由一种黏附和损伤性细菌病原体对肠道杯状细胞功能的调节。
Infect Immun. 2008 Feb;76(2):796-811. doi: 10.1128/IAI.00093-07. Epub 2007 Nov 5.
5
Toll-like receptor 4 contributes to colitis development but not to host defense during Citrobacter rodentium infection in mice.Toll样受体4在小鼠感染鼠柠檬酸杆菌期间对结肠炎的发展有促进作用,但对宿主防御无作用。
Infect Immun. 2006 May;74(5):2522-36. doi: 10.1128/IAI.74.5.2522-2536.2006.
6
Central role for B lymphocytes and CD4+ T cells in immunity to infection by the attaching and effacing pathogen Citrobacter rodentium.B淋巴细胞和CD4 + T细胞在抗黏附和损伤性病原菌鼠柠檬酸杆菌感染免疫中起核心作用。
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7
Mice lacking T and B lymphocytes develop transient colitis and crypt hyperplasia yet suffer impaired bacterial clearance during Citrobacter rodentium infection.缺乏T淋巴细胞和B淋巴细胞的小鼠会出现短暂性结肠炎和隐窝增生,但在感染鼠柠檬酸杆菌期间细菌清除能力受损。
Infect Immun. 2002 Apr;70(4):2070-81. doi: 10.1128/IAI.70.4.2070-2081.2002.
8
Intimin-specific immune responses prevent bacterial colonization by the attaching-effacing pathogen Citrobacter rodentium.紧密黏附素特异性免疫反应可阻止具紧密黏附作用的病原菌啮齿柠檬酸杆菌的细菌定植。
Infect Immun. 2001 Sep;69(9):5597-605. doi: 10.1128/IAI.69.9.5597-5605.2001.
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Citrobacter rodentium translocated intimin receptor (Tir) is an essential virulence factor needed for actin condensation, intestinal colonization and colonic hyperplasia in mice.鼠柠檬酸杆菌转位紧密黏附素受体(Tir)是小鼠肌动蛋白凝聚、肠道定植和结肠增生所必需的一种关键毒力因子。
Mol Microbiol. 2003 Apr;48(1):95-115. doi: 10.1046/j.1365-2958.2003.03429.x.
10
Host susceptibility to the attaching and effacing bacterial pathogen Citrobacter rodentium.宿主对黏附和损伤性细菌病原体鼠柠檬酸杆菌的易感性。
Infect Immun. 2003 Jun;71(6):3443-53. doi: 10.1128/IAI.71.6.3443-3453.2003.

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Dietary Salt Administration Decreases Enterotoxigenic (ETBF)-Promoted Tumorigenesis via Inhibition of Colonic Inflammation.膳食盐摄入可通过抑制结肠炎症减少肠产毒性(ETBF)促进的肿瘤发生。
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本文引用的文献

1
Salmonella pathogenicity island 2 mediates protection of intracellular Salmonella from reactive nitrogen intermediates.沙门氏菌致病岛2介导细胞内沙门氏菌免受活性氮中间体的侵害。
J Exp Med. 2002 May 6;195(9):1155-66. doi: 10.1084/jem.20011547.
2
Lipopolysaccharide-induced enterocyte-derived nitric oxide induces intestinal monolayer permeability in an autocrine fashion.脂多糖诱导肠上皮细胞衍生的一氧化氮以自分泌方式诱导肠道单层通透性。
Shock. 2002 Mar;17(3):180-4. doi: 10.1097/00024382-200203000-00004.
3
Mice lacking T and B lymphocytes develop transient colitis and crypt hyperplasia yet suffer impaired bacterial clearance during Citrobacter rodentium infection.缺乏T淋巴细胞和B淋巴细胞的小鼠会出现短暂性结肠炎和隐窝增生,但在感染鼠柠檬酸杆菌期间细菌清除能力受损。
Infect Immun. 2002 Apr;70(4):2070-81. doi: 10.1128/IAI.70.4.2070-2081.2002.
4
Colonic production of nitric oxide gas in ulcerative colitis, collagenous colitis and uninflamed bowel.溃疡性结肠炎、胶原性结肠炎及未发炎肠段中结肠一氧化氮气体的产生
Scand J Gastroenterol. 2002 Feb;37(2):183-8. doi: 10.1080/003655202753416858.
5
Impaired resistance and enhanced pathology during infection with a noninvasive, attaching-effacing enteric bacterial pathogen, Citrobacter rodentium, in mice lacking IL-12 or IFN-gamma.在缺乏白细胞介素-12或干扰素-γ的小鼠中,感染非侵袭性、黏附-侵蚀性肠道细菌病原体啮齿柠檬酸杆菌期间,抵抗力受损且病理状况加重。
J Immunol. 2002 Feb 15;168(4):1804-12. doi: 10.4049/jimmunol.168.4.1804.
6
The global regulator ArcA controls resistance to reactive nitrogen and oxygen intermediates in Salmonella enterica serovar Enteritidis.全局调控因子ArcA控制肠炎沙门氏菌肠炎血清型对活性氮和氧中间体的抗性。
Infect Immun. 2002 Feb;70(2):451-61. doi: 10.1128/IAI.70.2.451-461.2002.
7
Salmonella evasion of the NADPH phagocyte oxidase.沙门氏菌对NADPH吞噬细胞氧化酶的逃避
Microbes Infect. 2001 Nov-Dec;3(14-15):1313-20. doi: 10.1016/s1286-4579(01)01492-7.
8
Implications of Salmonella-induced nitric oxide (NO) for host defense and vaccines: NO, an antimicrobial, antitumor, immunosuppressive and immunoregulatory molecule.沙门氏菌诱导产生的一氧化氮(NO)对宿主防御及疫苗的影响:NO,一种具有抗菌、抗肿瘤、免疫抑制及免疫调节作用的分子。
Microbes Infect. 2001 Nov-Dec;3(14-15):1223-31. doi: 10.1016/s1286-4579(01)01482-4.
9
Molecular regulation of urothelial renewal and host defenses during infection with uropathogenic Escherichia coli.致病性大肠杆菌感染期间尿路上皮更新和宿主防御的分子调控
J Biol Chem. 2002 Mar 1;277(9):7412-9. doi: 10.1074/jbc.M110560200. Epub 2001 Dec 13.
10
Helicobacter pylori arginase inhibits nitric oxide production by eukaryotic cells: a strategy for bacterial survival.幽门螺杆菌精氨酸酶抑制真核细胞一氧化氮的产生:一种细菌生存策略。
Proc Natl Acad Sci U S A. 2001 Nov 20;98(24):13844-9. doi: 10.1073/pnas.241443798.

感染小鼠中黏附和损伤性细菌病原体鼠柠檬酸杆菌对诱导型一氧化氮合酶表达的调节

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

作者信息

Vallance Bruce A, Deng Wanyin, De Grado Myriam, Chan Crystal, Jacobson Kevan, Finlay B Brett

机构信息

Biotechnology Laboratory, University of British Columbia, Vancouver, British Columbia, Canada V6T 1Z3.

出版信息

Infect Immun. 2002 Nov;70(11):6424-35. doi: 10.1128/IAI.70.11.6424-6435.2002.

DOI:10.1128/IAI.70.11.6424-6435.2002
PMID:12379723
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC130393/
Abstract

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.

摘要

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。