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十二指肠贾第鞭毛虫感染中半胱氨酸蛋白酶依赖性黏液破坏及黏蛋白基因表达差异

Cysteine Protease-Dependent Mucous Disruptions and Differential Mucin Gene Expression in Giardia duodenalis Infection.

作者信息

Amat Christina B, Motta Jean-Paul, Fekete Elena, Moreau France, Chadee Kris, Buret Andre G

机构信息

Department of Biological Sciences, University of Calgary, Calgary, Alberta, Canada.

Department of Microbiology, Immunology and Infectious Diseases, Cumming School of Medicine, Calgary, Alberta, Canada.

出版信息

Am J Pathol. 2017 Nov;187(11):2486-2498. doi: 10.1016/j.ajpath.2017.07.009. Epub 2017 Aug 18.

Abstract

The intestinal mucous layer provides a critical host defense against pathogen exposure and epithelial injury, yet little is known about how enteropathogens may circumvent this physiologic barrier. Giardia duodenalis is a small intestinal parasite responsible for diarrheal disease and chronic postinfectious illness. This study reveals a complex interaction at the surface of epithelial cells, between G. duodenalis and the intestinal mucous layer. Here, we reveal mechanisms whereby G. duodenalis evades and disrupts the first line of host defense by degrading human mucin-2 (MUC2), depleting mucin stores and inducing differential gene expression in the mouse small and large intestines. Human colonic biopsy specimens exposed to G. duodenalis were depleted of mucus, and in vivo mice infected with G. duodenalis had a thinner mucous layer and demonstrated differential Muc2 and Muc5ac mucin gene expression. Infection in Muc2 mice elevated trophozoite colonization in the small intestine and impaired weight gain. In vitro, human LS174T goblet-like cells were depleted of mucus and had elevated levels of MUC2 mRNA expression after G. duodenalis exposure. Importantly, the cysteine protease inhibitor E64 prevented mucous degradation, mucin depletion, and the increase in MUC2 expression. This article describes a novel role for Giardia's cysteine proteases in pathogenesis and how Giardia's disruptions of the mucous barrier facilitate bacterial translocation that may contribute to the onset and propagation of disease.

摘要

肠道黏液层为抵御病原体暴露和上皮损伤提供了关键的宿主防御机制,但对于肠道病原体如何规避这一生理屏障却知之甚少。十二指肠贾第鞭毛虫是一种导致腹泻病和慢性感染后疾病的小肠寄生虫。本研究揭示了十二指肠贾第鞭毛虫与肠道黏液层在上皮细胞表面的复杂相互作用。在此,我们揭示了十二指肠贾第鞭毛虫通过降解人黏蛋白 -2(MUC2)、消耗黏蛋白储备以及诱导小鼠小肠和大肠中的基因差异表达来逃避和破坏宿主第一道防线的机制。暴露于十二指肠贾第鞭毛虫的人结肠活检标本黏液减少,感染十二指肠贾第鞭毛虫的体内小鼠黏液层变薄,并表现出Muc2和Muc5ac黏蛋白基因的差异表达。Muc2基因敲除小鼠感染后,滋养体在小肠中的定植增加,体重增加受损。在体外,人LS174T杯状样细胞在暴露于十二指肠贾第鞭毛虫后黏液减少,MUC2 mRNA表达水平升高。重要的是,半胱氨酸蛋白酶抑制剂E64可防止黏液降解、黏蛋白消耗以及MUC2表达增加。本文描述了贾第鞭毛虫半胱氨酸蛋白酶在发病机制中的新作用,以及贾第鞭毛虫对黏液屏障的破坏如何促进细菌易位,这可能有助于疾病的发生和传播。

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