Abstract:
: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.
journal_name
Nat Medjournal_title
Nature medicineauthors
Chen W,Calvo PA,Malide D,Gibbs J,Schubert U,Bacik I,Basta S,O'Neill R,Schickli J,Palese P,Henklein P,Bennink JR,Yewdell JWdoi
10.1038/nm1201-1306keywords:
subject
Has Abstractpub_date
2001-12-01 00:00:00pages
1306-12issue
12eissn
1078-8956issn
1546-170Xpii
nm1201-1306journal_volume
7pub_type
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