Positive effect of the hepatitis C virus nonstructural 5A protein on viral multiplication

Arch Virol. 2004 Jul;149(7):1353-71. doi: 10.1007/s00705-003-0291-6. Epub 2004 Mar 17.

Abstract

Hepatitis C virus infection (HCV), is a major cause of liver disease worldwide, and are frequently resistant to the interferon alpha treatment. The nonstructural (NS) 5A protein of HCV has been proposed to be involved in this resistance. Additional studies have pointed out a role for NS5A in several other cellular interactions as well as an important role of its adaptative mutations in HCV genome replication. However, no infectious system is available to assess the role of NS5A in the HCV life cycle. Thus, we have constructed a recombinant system directly demonstrating for the first time that the expression of NS5A confers a multiplicative advantage to Sindbis virus, a virus close to HCV. This advantage seemed to be related to an anti-apoptotic effect of the NS5A protein. At a later stage, a possible nuclear localization of NS5A was observed, likely due to apoptotic cleavages of this protein. The NS5A protein was also shown to induce the interleukin-8 (IL-8) mRNA and to activate the NF-kappaB pathway independently of the Sindbis virus. Together, our data suggest that the activation of NF-kappaB could lead to the anti-apoptotic activity of NS5A and explain the viral multiplicative advantage conferred by the expression of the NS5A protein.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis
  • Cell Nucleus / metabolism
  • Gene Expression Regulation, Viral
  • Genes, Reporter
  • Green Fluorescent Proteins
  • HeLa Cells
  • Hepacivirus / genetics
  • Hepacivirus / physiology*
  • Humans
  • Interleukin-8 / genetics
  • Interleukin-8 / metabolism
  • Luciferases / genetics
  • Luciferases / metabolism
  • Luminescent Proteins / metabolism
  • NF-kappa B / genetics
  • NF-kappa B / metabolism
  • RNA, Messenger / analysis
  • Recombinant Proteins / metabolism
  • Sindbis Virus / genetics
  • Sindbis Virus / physiology*
  • Viral Nonstructural Proteins / genetics
  • Viral Nonstructural Proteins / metabolism*
  • Viral Proteins / genetics
  • Viral Proteins / metabolism
  • Virus Replication*

Substances

  • Interleukin-8
  • Luminescent Proteins
  • NF-kappa B
  • NS-5 protein, hepatitis C virus
  • RNA, Messenger
  • Recombinant Proteins
  • Viral Nonstructural Proteins
  • Viral Proteins
  • pK3 protein, Vaccinia virus
  • Green Fluorescent Proteins
  • Luciferases