Expression of flavivirus capsids enhance the cellular environment for viral replication by activating Akt-signalling pathways

Virology. 2018 Mar:516:147-157. doi: 10.1016/j.virol.2018.01.009. Epub 2018 Jan 19.

Abstract

Flaviviruses depend on multiple host pathways during their life cycles and have evolved strategies to avoid the innate immune response. Previously, we showed that the West Nile virus capsid protein plays a role in this process by blocking apoptosis. In this study, we examined how expression of capsid proteins from several flaviviruses affects apoptosis and other host processes that impact virus replication. All of the tested capsid proteins protected cells from Fas-dependent apoptosis through a mechanism that requires activated Akt. Capsid expression upregulated other Akt-dependent cellular processes including expression of glucose transporter 1 and mitochondrial metabolism. Protein phosphatase 1, which is known to inactivate Akt, was identified as a DENV capsid interacting protein. This suggests that DENV capsid expression activates Akt by sequestering phosphatases that downregulate phospho-Akt. Capsid-dependent upregulation of Akt would enhance downstream signalling pathways that affect cell survival and metabolism, thus providing a favourable environment for virus replication.

Keywords: Akt-signalling; Apoptosis; Capsid; Dengue virus; Flavivirus; Protein phosphatase-1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis
  • Capsid / metabolism
  • Capsid Proteins / genetics
  • Capsid Proteins / metabolism*
  • Dengue Virus / genetics
  • Dengue Virus / physiology
  • Flavivirus / classification
  • Flavivirus / genetics
  • Flavivirus / metabolism
  • Flavivirus / physiology*
  • Flavivirus Infections / enzymology*
  • Flavivirus Infections / genetics
  • Flavivirus Infections / physiopathology
  • Flavivirus Infections / virology*
  • Humans
  • Phosphorylation
  • Protein Phosphatase 1 / genetics
  • Protein Phosphatase 1 / metabolism
  • Proto-Oncogene Proteins c-akt / genetics
  • Proto-Oncogene Proteins c-akt / metabolism*
  • Signal Transduction
  • Virus Replication*

Substances

  • Capsid Proteins
  • Proto-Oncogene Proteins c-akt
  • Protein Phosphatase 1