MG-132 reduces virus release in Bovine herpesvirus-1 infection

Sci Rep. 2017 Oct 17;7(1):13306. doi: 10.1038/s41598-017-13717-1.

Abstract

Bovine herpesvirus 1 (BoHV-1) can provoke conjunctivitis, abortions and shipping fever. BoHV-1 infection can also cause immunosuppression and increased susceptibility to secondary bacterial infections, leading to pneumonia and occasionally to death. Herein, we investigated the influence of MG-132, a proteasome inhibitor, on BoHV-1 infection in bovine kidney (MDBK) cells. Infection of MDBK cells with BoHV-1 induces apoptotic cell death that enhances virus release. Whereas, MG-132 inhibited virus-induced apoptosis and stimulated autophagy. Protein expression of viral infected cell protein 0 (bICP0), which is constitutively expressed during infection and is able to stimulate Nuclear factor kappa B (NF-κB), was completely inhibited by MG-132. These results were accompanied by a significant delay in the NF-κB activation. Interestingly, the efficient virus release provoked by BoHV-1-induced apoptosis was significantly reduced by MG-132. Overall, this study suggests that MG-132, through the activation of autophagy, may limit BoHV-1 replication during productive infection, by providing an antiviral defense mechanism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis
  • Autophagy
  • Cattle
  • Cell Line
  • Herpesvirus 1, Bovine / physiology*
  • Leupeptins / pharmacology*
  • NF-kappa B / metabolism
  • Proteasome Inhibitors / pharmacology*
  • Virus Release / drug effects*

Substances

  • Leupeptins
  • NF-kappa B
  • Proteasome Inhibitors
  • benzyloxycarbonylleucyl-leucyl-leucine aldehyde