Coxsackievirus protein 2BC blocks host cell apoptosis by inhibiting caspase-3

J Biol Chem. 2006 Jun 16;281(24):16296-304. doi: 10.1074/jbc.M510662200. Epub 2006 Apr 11.

Abstract

Virus infection may induce host cell death by apoptosis, but some DNA viruses are capable of preventing this process. RNA viruses were thought not to display anti-apoptotic activities, as their spread appears to benefit from a rapid induction of cell death. Here, we report an antiapoptotic activity in the Picornavirus Coxsackievirus B4 (CVB4). CVB4 infection of HeLa cells induced negligible apoptosis over a period of 10 h. However, infected cells developed resistance to drug-induced apoptosis using staurosporine and actinomycin D and to death receptor-induced apoptosis using tumor necrosis factor-related apoptosis-inducing ligand. Despite this resistance, the apoptotic machinery was nonetheless fully activated in these drug-treated infected cells because the levels of pro-caspase-3 processing to its active form were similar to control cells. However, the DEVDase (Asp-Glu-Val-Asp protease) activity of the processed caspase was significantly inhibited in the virus-infected staurosporine-treated cells compared with drug treatment alone. Likewise, extracts of CVB4-infected cells suppressed recombinant caspase-3 activity in vitro. Immunoprecipitation of activated caspase-3 from radiolabeled virus-infected cells revealed the co-precipitation of a 48-kDa protein that was tentatively identified as viral protein 2BC. Recombinant caspase-3 was found to co-precipitate with virus protein 2BC. Finally, when protein 2BC was expressed in HeLa cells, both staurosporine-induced apoptosis and in vitro caspase-3 DEVDase activity were significantly reduced. Taken together these data imply that CVB4 infection suppresses apoptosis through virus protein 2BC associating with caspase-3 and inhibiting its function. Thus, 2BC is the first reported RNA virus inhibitor of apoptosis protein.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Apoptosis Regulatory Proteins / metabolism
  • Apoptosis*
  • Caspase 3
  • Caspase Inhibitors*
  • Caspases / metabolism
  • Dactinomycin / pharmacology
  • Enterovirus*
  • Enzyme Inhibitors / pharmacology*
  • Flow Cytometry
  • HeLa Cells
  • Humans
  • Membrane Glycoproteins / metabolism
  • Molecular Sequence Data
  • Recombinant Proteins / chemistry
  • Sequence Homology, Amino Acid
  • TNF-Related Apoptosis-Inducing Ligand
  • Tumor Necrosis Factor-alpha / metabolism
  • Viral Nonstructural Proteins / metabolism*

Substances

  • Apoptosis Regulatory Proteins
  • Caspase Inhibitors
  • Enzyme Inhibitors
  • Membrane Glycoproteins
  • Recombinant Proteins
  • TNF-Related Apoptosis-Inducing Ligand
  • TNFSF10 protein, human
  • Tumor Necrosis Factor-alpha
  • Viral Nonstructural Proteins
  • Dactinomycin
  • CASP3 protein, human
  • Caspase 3
  • Caspases