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Mucosal Inflammatory Response to Salmonella typhimurium Infection.鼠伤寒沙门氏菌感染的黏膜炎症反应
Front Immunol. 2014 Jul 4;5:311. doi: 10.3389/fimmu.2014.00311. eCollection 2014.
2
Neutrophils are a source of gamma interferon during acute Salmonella enterica serovar Typhimurium colitis.中性粒细胞是沙门氏菌肠炎时γ干扰素的来源。
Infect Immun. 2014 Apr;82(4):1692-7. doi: 10.1128/IAI.01508-13. Epub 2014 Jan 13.
3
Altered expression and localization of ion transporters contribute to diarrhea in mice with Salmonella-induced enteritis.离子转运体的表达和定位改变导致沙门氏菌诱导的肠炎小鼠腹泻。
Gastroenterology. 2013 Dec;145(6):1358-1368.e1-4. doi: 10.1053/j.gastro.2013.08.054. Epub 2013 Aug 31.
4
Control of neutrophil inflammation at mucosal surfaces by secreted epithelial products.黏膜表面分泌的上皮产物对中性粒细胞炎症的控制。
Front Immunol. 2013 Jul 31;4:220. doi: 10.3389/fimmu.2013.00220. eCollection 2013.
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Outbreak-associated Salmonella enterica serotypes and food Commodities, United States, 1998-2008.1998-2008 年美国与疫情相关的沙门氏菌血清型和食品类别。
Emerg Infect Dis. 2013 Aug;19(8):1239-44. doi: 10.3201/eid1908.121511.
6
Salmonella uses energy taxis to benefit from intestinal inflammation.沙门氏菌利用能量趋药性来获益于肠道炎症。
PLoS Pathog. 2013;9(4):e1003267. doi: 10.1371/journal.ppat.1003267. Epub 2013 Apr 18.
7
Diarrhea and colitis in mice require the Salmonella pathogenicity island 2-encoded secretion function but not SifA or Spv effectors.腹泻和结肠炎在小鼠中需要沙门氏菌致病岛 2 编码的分泌功能,但不需要 SifA 或 Spv 效应子。
Infect Immun. 2012 Oct;80(10):3360-70. doi: 10.1128/IAI.00404-12. Epub 2012 Jul 9.
8
Salmonella transiently reside in luminal neutrophils in the inflamed gut.沙门氏菌在发炎肠道的腔道中性粒细胞中短暂定植。
PLoS One. 2012;7(4):e34812. doi: 10.1371/journal.pone.0034812. Epub 2012 Apr 6.
9
International spread of an epidemic population of Salmonella enterica serotype Kentucky ST198 resistant to ciprofloxacin.耐环丙沙星的肠炎沙门氏菌血清型肯塔基 ST198 的流行株在国际上的传播。
J Infect Dis. 2011 Sep 1;204(5):675-84. doi: 10.1093/infdis/jir409. Epub 2011 Aug 2.
10
Deaths associated with bacterial pathogens transmitted commonly through food: foodborne diseases active surveillance network (FoodNet), 1996-2005.与通过食物常见传播的细菌病原体相关的死亡:食源性疾病主动监测网络(FoodNet),1996-2005 年。
J Infect Dis. 2011 Jul 15;204(2):263-7. doi: 10.1093/infdis/jir263.

沙门氏菌引起的腹泻在缺乏白细胞介素8受体(CXCR2)依赖性中性粒细胞炎症的情况下发生。

Salmonella-induced Diarrhea Occurs in the Absence of IL-8 Receptor (CXCR2)-Dependent Neutrophilic Inflammation.

作者信息

Marchelletta Ronald R, Gareau Melanie G, Okamoto Sharon, Guiney Donald G, Barrett Kim E, Fierer Joshua

机构信息

Division of Gastroenterology.

Division of Infectious Diseases, University of California, San Diego, School of Medicine, La Jolla.

出版信息

J Infect Dis. 2015 Jul 1;212(1):128-36. doi: 10.1093/infdis/jiu829. Epub 2014 Dec 23.

DOI:10.1093/infdis/jiu829
PMID:25538271
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4542593/
Abstract

BACKGROUND

Gastroenteritis is the most common manifestation of nontyphoidal Salmonella enterica infections, but little is known about the pathogenesis of diarrhea in this infection

METHODS

To determine whether polymorphonuclear neutrophils (PMNs) are required for diarrhea for Salmonella colitis, we infected kanamycin-pretreated interleukin 8R (IL-8R) mutant mice and controls, both with nonmutant Slc11a1 (Nramp1, ItyR). We compared the 2 mouse strains for increases in fecal water content (diarrhea) 3 days after infection, changes in expression of ion transporters in colonic epithelial cells, proliferation of epithelial cells, and severity of infection as measured by colony-forming units (CFUs).

RESULTS

The IL-8R knockout mice had fewer PMNs in the colon but the other variables we measured were unaffected except for an increase in CFUs in the colon. The pathologic changes in the cecum were similar in both groups except for the lack of PMNs in the IL-8R knockout mice. There was minimal damage to the colon more distally.

CONCLUSIONS

In the early stage of Salmonella colitis, PMNs are not required for diarrhea or for the decrease in expression of colonic epithelial cell apical ion transporters. They contribute to defense against infection in the cecum but not extracolonically at this stage of Salmonella colitis.

摘要

背景

肠胃炎是非伤寒型肠炎沙门氏菌感染最常见的表现形式,但对于这种感染中腹泻的发病机制知之甚少。

方法

为了确定沙门氏菌结肠炎腹泻是否需要多形核中性粒细胞(PMN),我们用非突变型Slc11a1(Nramp1,ItyR)感染了经卡那霉素预处理的白细胞介素8受体(IL-8R)突变小鼠和对照小鼠。我们比较了这两种小鼠品系在感染后3天粪便含水量(腹泻)的增加情况、结肠上皮细胞中离子转运体表达的变化、上皮细胞的增殖以及通过菌落形成单位(CFU)测量的感染严重程度。

结果

IL-8R基因敲除小鼠结肠中的PMN较少,但除了结肠中CFU增加外,我们测量的其他变量均未受影响。两组盲肠的病理变化相似,只是IL-8R基因敲除小鼠中没有PMN。更远端的结肠损伤最小。

结论

在沙门氏菌结肠炎的早期阶段,腹泻或结肠上皮细胞顶端离子转运体表达的降低并不需要PMN。它们有助于在盲肠中抵御感染,但在沙门氏菌结肠炎的这个阶段,在结肠外没有作用。