Entry of influenza A virus: host factors and antiviral targets

被引:159
|
作者
Edinger, Thomas O. [1 ]
Pohl, Marie O. [1 ]
Stertz, Silke [1 ]
机构
[1] Univ Zurich, Inst Med Virol, CH-8057 Zurich, Switzerland
来源
关键词
NUCLEAR-LOCALIZATION SIGNAL; RECEPTOR-BINDING; CONFORMATIONAL-CHANGE; MATRIX PROTEIN; MEMBRANE-FUSION; LOW-PH; M2; PROTEIN; ANTIINFLUENZA ACTION; INFECTIOUS ENTRY; MANNOSE RECEPTOR;
D O I
10.1099/vir.0.059477-0
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Influenza virus is a major human pathogen that causes annual epidemics and occasional "pandemics. Moreover, the virus causes outbreaks in poultry and other animals, such as pigs, requiring costly and laborious countermeasures. Therefore, influenza virus has a substantial impact on health and the global economy. Here, we review entry of this important pathogen into target cells, an essential process by which viral genomes are delivered from extracellular virions to sites of transcription/replication in the cell nucleus. We summarize current knowledge on the interaction of influenza viruses with their receptor, sialic acid, and highlight the ongoing search for additional receptors. We describe receptor-mediated endocytosis and the recently discovered macropinocytosis as alternative virus uptake pathways, and illustrate the subsequent endosomal trafficking of the virus with advanced live microscopy techniques. Release of virus from the endosome and import of the viral ribonucleoproteins into the host cell nucleus are also outlined. Although a focus has been on viral protein function during entry, recent studies have revealed exciting information on cellular factors required for influenza virus entry. We highlight these, and discuss established entry inhibitors targeting viral and host factors, as well as the latest prospects for designing novel 'anti-entry' compounds. New entry inhibitors are of particular importance for current efforts to develop the next generation of anti-influenza drugs entry is the first essential step of virus replication and is an ideal target to block infection efficiently.
引用
收藏
页码:263 / 277
页数:15
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