Frontiers in Immunology (Nov 2022)

Porcine sapelovirus 2A protein induces mitochondrial-dependent apoptosis

  • Chunxiao Mou,
  • Chunxiao Mou,
  • Chunxiao Mou,
  • Yuxi Wang,
  • Shuonan Pan,
  • Kaichuang Shi,
  • Zhenhai Chen,
  • Zhenhai Chen,
  • Zhenhai Chen

DOI
https://doi.org/10.3389/fimmu.2022.1050354
Journal volume & issue
Vol. 13

Abstract

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Porcine sapelovirus (PSV) is an emerging pathogen associated with symptoms of enteritis, pneumonia, polioencephalomyelitis and reproductive disorders in swine, resulting in significant economic losses. Although PSV is reported to trigger cell apoptosis, its specific molecular mechanism is unclear. In this research, the cell apoptosis induced by PSV infection and its underlying mechanisms were investigated. The morphologic features of apoptosis include nuclear condensation and fragmentation, were observed after PSV infection. The cell apoptosis was confirmed by analyzing the apoptotic rates, caspase activation, and PARP1 cleavage. Caspase inhibitors inhibited the PSV-induced intrinsic apoptosis pathway and reduced viral replication. Among the proteins encoded by PSV, 2A is an important factor in inducing the mitochondrial apoptotic pathway. The conserved residues H48, D91, and C164 related to protease activity in PSV 2A were crucial for 2A-induced apoptosis. In conclusion, our results provide insights into how PSV induces host cell apoptosis.

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