Institute of Virology, Philipps-University Marburg, Marburg, Germany.
Pathog Dis. 2013 Nov;69(2):87-100. doi: 10.1111/2049-632X.12053. Epub 2013 Jul 2.
Influenza is an acute infection of the respiratory tract, which affects each year millions of people. Influenza virus infection is initiated by the surface glycoprotein hemagglutinin (HA) through receptor binding and fusion of viral and endosomal membranes. HA is synthesized as a precursor protein and requires cleavage by host cell proteases to gain its fusion capacity. Although cleavage of HA is crucial for virus infectivity, little was known about relevant proteases in the human airways for a long time. Recent progress in the identification and characterization of HA-activating host cell proteases has been considerable however and supports the idea of targeting HA cleavage as a novel approach for influenza treatment. Interestingly, certain bacteria have been demonstrated to support HA activation either by secreting proteases that cleave HA or due to activation of cellular proteases and thereby may contribute to virus spread and enhanced pathogenicity. In this review, we give an overview on activation of influenza viruses by proteases from host cells and bacteria with the main focus on recent progress on HA cleavage by proteases HAT and TMPRSS2 in the human airway epithelium. In addition, we outline investigations of HA-activating proteases as potential drug targets for influenza treatment.
流感是一种急性呼吸道感染,每年影响数百万人。流感病毒感染是由表面糖蛋白血凝素 (HA) 通过受体结合和病毒与内体膜融合启动的。HA 作为前体蛋白合成,需要宿主细胞蛋白酶的切割才能获得融合能力。尽管 HA 的切割对于病毒感染性至关重要,但很长一段时间以来,人们对人类气道中相关蛋白酶知之甚少。然而,近年来在鉴定和表征 HA 激活宿主细胞蛋白酶方面取得了相当大的进展,这支持了将 HA 切割作为流感治疗新方法的想法。有趣的是,某些细菌已被证明通过分泌切割 HA 的蛋白酶或通过激活细胞蛋白酶来支持 HA 激活,从而可能有助于病毒传播和致病性增强。在这篇综述中,我们概述了宿主细胞和细菌中的蛋白酶对流感病毒的激活作用,重点介绍了人类气道上皮细胞中 HAT 和 TMPRSS2 蛋白酶对 HA 切割的最新进展。此外,我们还概述了将 HA 激活蛋白酶作为流感治疗潜在药物靶点的研究。