The PI3K/Akt pathway contributes to arenavirus budding

J Virol. 2012 Apr;86(8):4578-85. doi: 10.1128/JVI.06604-11. Epub 2012 Feb 15.

Abstract

Several arenaviruses, chiefly Lassa virus (LASV), cause hemorrhagic fever (HF) disease in humans and pose a significant public health concern in regions where they are endemic. On the other hand, evidence indicates that the globally distributed prototypic arenavirus lymphocytic choriomeningitis virus (LCMV) is a neglected human pathogen. The phosphatidylinositol 3-kinase (PI3K)/Akt pathway participates in many cellular processes, including cell survival and differentiation, and also has been shown to play important roles in different steps of the life cycles of a variety of viruses. Here we report that the inhibition of the PI3K/Akt pathway inhibited budding and to a lesser extent RNA synthesis, but not cell entry, of LCMV. Accordingly, BEZ-235, a PI3K inhibitor currently in cancer clinical trials, inhibited LCMV multiplication in cultured cells. These findings, together with those previously reported for Junin virus (JUNV), indicate that targeting the PI3K/Akt pathway could represent a novel antiviral strategy to combat human-pathogenic arenaviruses.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Arenavirus / drug effects
  • Arenavirus / genetics
  • Arenavirus / metabolism*
  • Cell Line
  • Chlorocebus aethiops
  • Chromones / pharmacology
  • Gene Expression Regulation, Viral / drug effects
  • Humans
  • Imidazoles / pharmacology
  • Lassa virus / drug effects
  • Lassa virus / genetics
  • Lassa virus / metabolism
  • Lymphocytic choriomeningitis virus / drug effects
  • Lymphocytic choriomeningitis virus / genetics
  • Lymphocytic choriomeningitis virus / metabolism
  • Morpholines / pharmacology
  • Phosphatidylinositol 3-Kinases / metabolism*
  • Phosphoinositide-3 Kinase Inhibitors
  • Proto-Oncogene Proteins c-akt / antagonists & inhibitors
  • Proto-Oncogene Proteins c-akt / metabolism*
  • Quinolines / pharmacology
  • RNA, Viral / metabolism
  • Signal Transduction* / drug effects
  • Sirolimus / pharmacology
  • Virus Internalization / drug effects
  • Virus Release* / drug effects
  • Virus Replication / drug effects

Substances

  • Chromones
  • Imidazoles
  • Morpholines
  • Phosphoinositide-3 Kinase Inhibitors
  • Quinolines
  • RNA, Viral
  • 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one
  • Proto-Oncogene Proteins c-akt
  • dactolisib
  • Sirolimus