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鼠伤寒沙门氏菌的一种富含亮氨酸重复序列的转位效应蛋白可抑制NF-κB依赖性基因表达。

A Salmonella enterica serovar typhimurium translocated leucine-rich repeat effector protein inhibits NF-kappa B-dependent gene expression.

作者信息

Haraga Andrea, Miller Samuel I

机构信息

Department of Microbiology, University of Washington, Seattle, Washington 98195-7710, USA.

出版信息

Infect Immun. 2003 Jul;71(7):4052-8. doi: 10.1128/IAI.71.7.4052-4058.2003.

Abstract

Nontyphoidal salmonellae are enteric pathogens that cause acute gastroenteritis and colonize the intestinal tract for prolonged periods. In the intestinal epithelia, these bacteria induce secretion of proinflammatory cytokines, such as interleukin-8 (IL-8), which leads to a profound inflammatory response through recruitment of polymorphonuclear leukocytes. Production of IL-8 induced by Salmonella spp. is due to the activation of the transcription factors nuclear factor kappa B (NF-kappa B) and activator protein-1 (AP-1). This work demonstrates that Salmonella enterica serovar Typhimurium can downmodulate IL-8 production after invasion of intestinal epithelial cells. The Salmonella translocated effector proteins SspH1 and SptP participate in this process. SspH1 is a member of the bacterial LPX repeat protein family that localizes to the mammalian nucleus and inhibits NF-kappa B-dependent gene expression. A Shigella flexneri translocated effector, IpaH9.8, which has a similar structure and subcellular localization in mammalian cells, also inhibits NF-kappaB-dependent gene expression. We propose that suppression of inflammatory responses by intracellular S. enterica serovar Typhimurium, and perhaps Shigella flexneri, contributes to bacterial colonization of host tissues and pathogenesis.

摘要

非伤寒沙门氏菌是引起急性肠胃炎并能在肠道中长期定植的肠道病原体。在肠道上皮细胞中,这些细菌诱导促炎细胞因子如白细胞介素-8(IL-8)的分泌,通过募集多形核白细胞导致强烈的炎症反应。沙门氏菌属诱导的IL-8产生是由于转录因子核因子κB(NF-κB)和活化蛋白-1(AP-1)的激活。这项研究表明,鼠伤寒沙门氏菌肠炎血清型在侵入肠道上皮细胞后可下调IL-8的产生。沙门氏菌转运效应蛋白SspH1和SptP参与了这一过程。SspH1是细菌LPX重复蛋白家族的成员,定位于哺乳动物细胞核并抑制NF-κB依赖的基因表达。弗氏志贺氏菌转运效应蛋白IpaH9.8在哺乳动物细胞中具有相似的结构和亚细胞定位,也抑制NF-κB依赖的基因表达。我们提出,细胞内鼠伤寒沙门氏菌肠炎血清型以及可能还有弗氏志贺氏菌对炎症反应的抑制有助于细菌在宿主组织中的定植和发病机制。

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