A novel influenza A virus mitochondrial protein that induces cell death

被引:776
作者
Chen, WS
Calvo, PA
Malide, D
Gibbs, J
Schubert, U
Bacik, I
Basta, S
O'Neill, R
Schickli, J
Palese, P
Henklein, P
Bennink, JR
Yewdell, JW [1 ]
机构
[1] NIAID, Viral Dis Lab, Bethesda, MD 20892 USA
[2] Mt Sinai Sch Med, Dept Microbiol, New York, NY 10029 USA
[3] Univ Hamburg, Heinrich Pette Inst Expt Virol & Immunol, D-2000 Hamburg, Germany
[4] Humboldt Univ, Inst Biochem, Berlin, Germany
关键词
D O I
10.1038/nm1201-1306
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
While searching for alternative reading-frame peptides encoded by influenza A virus that are recognized by CD8(+)T cells, we found an abundant immunogenic peptide encoded by the +1 reading frame of PB1. This peptide derives from a novel conserved 87-residue protein, PB1-F2, which has several unusual features compared with other influenza gene products in addition to its mode of translation. These include its absence from some animal (particularly swine) influenza virus Isolates, variable expression in individual infected cells, rapid proteasome-dependent degradation and mitochondrial localization. Exposure of cells to a synthetic version of PB1-F2 induces apoptosis, and influenza viruses with targeted mutations that interfere with PB1-F2 expression Induce less extensive apoptosis in human monocytic cells than those with intact PB1-F2. We propose that PB1-F2 functions to kill host immune cells responding to influenza virus infection.
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页码:1306 / 1312
页数:7
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