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A novel influenza A virus mitochondrial protein that induces cell death

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.

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Figure 1: Characterization of PB1-F262–70 immunogenicity and antigenicity.
Figure 2: DNA and amino acid sequence of novel ORF in the PB1 gene.
Figure 3: Biochemical characterization of PB1-F2.
Figure 4: Intracellular localization of IAV-expressed PB1-F2.
Figure 5: Intracellular localization of transfected and microinjected PB1-F2.
Figure 6: PB1-F2 mediated induction of apoptosis.

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Acknowledgements

We thank B. Buschling for technical assistance; A. Weisberg for cryo-electron microscopy; K. Bruns for secondary structure predictions using NNPREDICT; D. Green for generously and expeditiously providing cytochrome c–transfected cells and unpublished data; and D. Tscharke for critical comments on the manuscript and assistance with the graphics.

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Correspondence to Jonathan W. Yewdell.

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Chen, W., Calvo, P., Malide, D. et al. A novel influenza A virus mitochondrial protein that induces cell death. Nat Med 7, 1306–1312 (2001). https://doi.org/10.1038/nm1201-1306

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