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干扰素-γ在沙门氏菌致病机制中的作用:老问题有新花样

Interferon-γ in Salmonella pathogenesis: New tricks for an old dog.

作者信息

Ingram Justin P, Brodsky Igor E, Balachandran Siddharth

机构信息

Blood Cell Development and Function Program, Fox Chase Cancer Center, Philadelphia, PA 19111, United States.

Department of Pathobiology, University of Pennsylvania School of Veterinary Medicine, Philadelphia, PA 19104, United States.

出版信息

Cytokine. 2017 Oct;98:27-32. doi: 10.1016/j.cyto.2016.10.009. Epub 2016 Oct 20.

Abstract

Salmonella enterica is a facultative intracellular bacterium that is the leading cause of food borne illnesses in humans. The cytokine IFN-γ has well-established antibacterial properties against Salmonella and other intracellular microbes, for example its capacity to activate macrophages, promote phagocytosis, and destroy phagocytosed microbes by free radical-driven toxification of phagosomes. But IFN-γ induces the expression of hundreds of uncharacterized genes, suggesting that this cytokine deploys additional antimicrobial strategies that await discovery. Recently, one such mechanism, mediated by a family of IFN-inducible small GTPases called Guanylate Binding Proteins (GBPs) has been uncovered. GBPs were shown to facilitate the pyroptotic clearance of Salmonella from infected macrophages by rupturing the protective intracellular vacuole this microbe forms around itself. Once this protective vacuole is lost, exposed Salmonella activates pyroptosis, which destroys the infected cell. In this review, we summarize such emerging roles for IFN-γ in restricting Salmonella pathogenesis.

摘要

肠炎沙门氏菌是一种兼性胞内细菌,是人类食源性疾病的主要病因。细胞因子干扰素-γ对沙门氏菌和其他胞内微生物具有公认的抗菌特性,例如它能够激活巨噬细胞、促进吞噬作用,并通过吞噬体的自由基驱动的毒性作用破坏被吞噬的微生物。但是干扰素-γ会诱导数百个未表征基因的表达,这表明这种细胞因子还部署了有待发现的其他抗菌策略。最近,一种由一类名为鸟苷酸结合蛋白(GBPs)的干扰素诱导型小GTP酶介导的机制被发现。研究表明,GBPs通过破坏这种微生物在自身周围形成的保护性胞内液泡,促进感染的巨噬细胞对沙门氏菌进行焦亡清除。一旦这种保护性液泡丧失,暴露的沙门氏菌就会激活焦亡,从而破坏被感染的细胞。在这篇综述中,我们总结了干扰素-γ在限制沙门氏菌发病机制方面的这些新出现的作用。

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