Mechanisms of Coronavirus Cell Entry Mediated by the Viral Spike Protein

被引:961
作者
Belouzard, Sandrine [2 ]
Millet, Jean K. [1 ]
Licitra, Beth N. [1 ]
Whittaker, Gary R. [1 ]
机构
[1] Cornell Univ, Dept Microbiol & Immunol, Ithaca, NY 14853 USA
[2] Univ Lille Nord France, Inst Pasteur Lille, INSERM U1019, Ctr Infect & Immun Lille,CNRS UMR8204, F-59000 Lille, France
来源
VIRUSES-BASEL | 2012年 / 4卷 / 06期
基金
美国国家卫生研究院;
关键词
coronavirus; spike; viral entry; fusion; proteolytic activation; RESPIRATORY SYNDROME CORONAVIRUS; MOUSE HEPATITIS-VIRUS; INFECTIOUS-BRONCHITIS VIRUS; TRANSMISSIBLE GASTROENTERITIS CORONAVIRUS; RECEPTOR-INDEPENDENT INFECTION; PUTATIVE FUSION PEPTIDE; ACID BINDING-ACTIVITY; CD209L L-SIGN; MURINE CORONAVIRUS; SARS-CORONAVIRUS;
D O I
10.3390/v4061011
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Coronaviruses are enveloped positive-stranded RNA viruses that replicate in the cytoplasm. To deliver their nucleocapsid into the host cell, they rely on the fusion of their envelope with the host cell membrane. The spike glycoprotein (S) mediates virus entry and is a primary determinant of cell tropism and pathogenesis. It is classified as a class I fusion protein, and is responsible for binding to the receptor on the host cell as well as mediating the fusion of host and viral membranes-A process driven by major conformational changes of the S protein. This review discusses coronavirus entry mechanisms focusing on the different triggers used by coronaviruses to initiate the conformational change of the S protein: receptor binding, low pH exposure and proteolytic activation. We also highlight commonalities between coronavirus S proteins and other class I viral fusion proteins, as well as distinctive features that confer distinct tropism, pathogenicity and host interspecies transmission characteristics to coronaviruses.
引用
收藏
页码:1011 / 1033
页数:23
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