Interferon-Induced Cell Membrane Proteins, IFITM3 and Tetherin, Inhibit Vesicular Stomatitis Virus Infection via Distinct Mechanisms

被引:258
作者
Weidner, Jessica M. [1 ]
Jiang, Dong [1 ]
Pan, Xiao-Ben [1 ]
Chang, Jinhong [1 ]
Block, Timothy M. [1 ,2 ]
Guo, Ju-Tao [1 ]
机构
[1] Drexel Univ, Coll Med, Drexel Inst Biotechnol & Virol Res, Dept Microbiol & Immunol, Doylestown, PA 18902 USA
[2] Hepatitis B Fdn, Inst Hepatitis Virus Res, Doylestown, PA 18902 USA
基金
美国国家卫生研究院;
关键词
WEST-NILE-VIRUS; STRANDED RNA; KINASE PKR; REPLICATION; IDENTIFICATION; RECOGNITION; RELEASE; FAMILY; RESISTANCE; RECEPTOR;
D O I
10.1128/JVI.01328-10
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Tetherin and IFITM3 are recently identified interferon-induced cellular proteins that restrict infections by retroviruses and filoviruses and of influenza virus and flaviviruses, respectively. In our efforts to further explore their antiviral activities against other viruses and determine their antiviral mechanisms, we found that the two antiviral proteins potently inhibit the infection of vesicular stomatitis virus (VSV), a prototype member of the Rhabdoviridae family. Taking advantage of this well-studied virus infection system, we show that although both tetherin and IFITM3 are plasma membrane proteins, tetherin inhibits virion particle release from infected cells, while IFITM3 disrupts an early event after endocytosis of virion particles but before primary transcription of incoming viral genomes. Furthermore, we demonstrate that both the N-terminal 21 amino acid residues and C-terminal transmembrane region of IFITM3 are required for its antiviral activity. Collectively, our work sheds light on the mechanisms by which tetherin and IFITM3 restrict infection with rhabdoviruses and possibly other pathogenic viruses.
引用
收藏
页码:12646 / 12657
页数:12
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