Novel insights into proteolytic cleavage of influenza virus hemagglutinin

被引:121
作者
Bertram, Stephanie [1 ]
Glowacka, Ilona [1 ]
Steffen, Imke [1 ]
Kuehl, Annika [1 ]
Poehlmann, Stefan [1 ]
机构
[1] Hannover Med Sch, Inst Virol, D-30625 Hannover, Germany
关键词
TRYPSIN-LIKE PROTEASE; TRANSMEMBRANE SERINE PROTEASES; RESPIRATORY SYNCYTIAL VIRUS; TOXIN PROTECTIVE ANTIGEN; HOST-CELL PROTEASES; A VIRUS; AVIAN INFLUENZA; MEMBRANE-FUSION; HUMAN AIRWAY; NEURAMINIDASE DETERMINES;
D O I
10.1002/rmv.657
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The influenza virus hemagglutinin (HA) mediates the first essential step in the viral life cycle, virus entry into target cells. Influenza virus HA is synthesised as a precursor protein in infected cells and requires cleavage by host cell proteases to transit into an active form. Cleavage is essential for influenza virus infectivity and the HA-processing proteases are attractive targets for therapeutic intervention. It is well established that cleavage by ubiquitously expressed subtilisin-like proteases is a hallmark of highly pathogenic avian influenza viruses (HPAIV). In contrast, the nature of the proteases responsible for cleavage of HA of human influenza viruses and low pathogenic avian influenza viruses (LPAIV) is not well understood. Recent studies suggest that cleavage of HA of human influenza viruses might be a cell-associated event and might be facilitated by the type II transmembrane serine proteases (TTSPs) TMPRSS2, TMPRSS4 and human airway trypsin-like protease (HAT). Here, we will introduce the different concepts established for proteolytic activation of influenza virus HA, with a particular focus on the role of TTSPs, and we will discuss their implications for viral tropism, pathogenicity and antiviral intervention. Copyright (C) 2010 John Wiley & Sons, Ltd.
引用
收藏
页码:298 / 310
页数:13
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