Mature viral cathepsin is required for release of viral occlusion bodies from Autographa californica multiple nucleopolyhedrovirus-infected cells

Virology. 2021 Apr:556:23-32. doi: 10.1016/j.virol.2021.01.001. Epub 2021 Jan 11.

Abstract

Baculovirus-infected larvae release progeny viral occlusion bodies (OBs) to enable cyclical virus transmission to new hosts. The alphabaculovirus chitinase and cathepsin enzymes cause terminal liquefaction of host insect cadavers, aiding OB dispersal. The mechanism of cell lysis required to release the OBs is unclear but here we show Autographa californica multiple nucleopolyhedrovirus cathepsin protease activity is required for efficient release of the host tissue-degrading chitinase and cathepsin enzymes and critical for release of progeny OBs from virus-infected cells. Comparisons between viruses containing or lacking cathepsin indicate that cathepsin was necessary for OB release into cultured cell media or hemolymph of insects. In addition, pharmacological inhibition of cysteine protease activity in cells during infection blocked maturation of active cathepsin and OB release from infected cells. Together, these results suggest an important link between baculovirus-induced cell lysis, the concomitant maturation of cathepsin, and cellular release of chitinase, cathepsin and progeny OBs from cells.

Keywords: Baculovirus; Cell lysis; Chitinase; Cysteine protease; Enzyme protein-protein interaction; Nuclear lysis; Virus release.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cathepsins / metabolism*
  • Cell Death
  • Cysteine Proteases / metabolism*
  • Nucleopolyhedroviruses / pathogenicity*
  • Occlusion Bodies, Viral / metabolism*
  • Sf9 Cells
  • Spodoptera
  • Viral Proteins / metabolism*

Substances

  • Viral Proteins
  • Cathepsins
  • Cysteine Proteases

Supplementary concepts

  • Autographa californica multiple nuclear polyhedrosis virus