[PDF][PDF] Phosphoprotein of human parainfluenza virus type 3 blocks autophagosome-lysosome fusion to increase virus production

B Ding, G Zhang, X Yang, S Zhang, L Chen, Q Yan… - Cell host & …, 2014 - cell.com
B Ding, G Zhang, X Yang, S Zhang, L Chen, Q Yan, M Xu, AK Banerjee, M Chen
Cell host & microbe, 2014cell.com
Autophagy is a multistep process in which cytoplasmic components, including invading
pathogens, are captured by autophagosomes that subsequently fuse with degradative
lysosomes. Negative-strand RNA viruses, including paramyxoviruses, have been shown to
alter autophagy, but the molecular mechanisms remain largely unknown. We demonstrate
that human parainfluenza virus type 3 (HPIV3) induces incomplete autophagy by blocking
autophagosome-lysosome fusion, resulting in increased virus production. The viral …
Summary
Autophagy is a multistep process in which cytoplasmic components, including invading pathogens, are captured by autophagosomes that subsequently fuse with degradative lysosomes. Negative-strand RNA viruses, including paramyxoviruses, have been shown to alter autophagy, but the molecular mechanisms remain largely unknown. We demonstrate that human parainfluenza virus type 3 (HPIV3) induces incomplete autophagy by blocking autophagosome-lysosome fusion, resulting in increased virus production. The viral phosphoprotein (P) is necessary and sufficient to inhibition autophagosome degradation. P binds to SNAP29 and inhibits its interaction with syntaxin17, thereby preventing these two host SNARE proteins from mediating autophagosome-lysome fusion. Incomplete autophagy and resultant autophagosome accumulation increase extracellular viral production but do not affect viral protein synthesis. These findings highlight how viruses can block autophagosome degradation by disrupting the function of SNARE proteins.
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