Mouse Norovirus infection promotes autophagy induction to facilitate replication but prevents final autophagosome maturation

Virology. 2016 May:492:130-9. doi: 10.1016/j.virol.2016.02.018. Epub 2016 Mar 21.

Abstract

Autophagy is a cellular process used to eliminate intracellular pathogens. Many viruses however are able to manipulate this cellular process for their own advantage. Here we demonstrate that Mouse Norovirus (MNV) infection induces autophagy but does not appear to utilise the autophagosomal membrane for establishment and formation of the viral replication complex. We have observed that MNV infection results in lipidation and recruitment of LC3 to the autophagosome membrane but prevents subsequent fusion of the autophagosomes with lysosomes, as SQSTM1 (an autophagy receptor) accumulates and Lysosome-Associated Membrane Protein1 is sequestered to the MNV replication complex (RC) rather than to autophagosomes. We have additionally observed that chemical modulation of autophagy differentially affects MNV replication. From this study we can conclude that MNV infection induces autophagy, however suppresses the final maturation step of this response, indicating that autophagy induction contributes to MNV replication independently of RC biogenesis.

Keywords: Autophagy; Mouse Norovirus; Virus replication.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing / genetics
  • Adaptor Proteins, Signal Transducing / metabolism
  • Animals
  • Autophagy / genetics*
  • Cell Line
  • Chlorocebus aethiops
  • Gene Expression Regulation
  • HEK293 Cells
  • Heat-Shock Proteins / genetics
  • Heat-Shock Proteins / metabolism
  • Host-Pathogen Interactions*
  • Humans
  • Intracellular Membranes / metabolism
  • Intracellular Membranes / ultrastructure
  • Intracellular Membranes / virology
  • Lysosomal Membrane Proteins / genetics
  • Lysosomal Membrane Proteins / metabolism
  • Macrophages / cytology
  • Macrophages / virology*
  • Mice
  • Microtubule-Associated Proteins / genetics*
  • Microtubule-Associated Proteins / metabolism
  • Norovirus / genetics*
  • Norovirus / metabolism
  • Phagosomes / metabolism
  • Phagosomes / ultrastructure
  • Phagosomes / virology*
  • Sequestosome-1 Protein
  • Signal Transduction
  • Vero Cells
  • Virus Replication / genetics

Substances

  • Adaptor Proteins, Signal Transducing
  • Heat-Shock Proteins
  • Lamp1 protein, mouse
  • Lysosomal Membrane Proteins
  • Map1lc3b protein, mouse
  • Microtubule-Associated Proteins
  • Sequestosome-1 Protein
  • Sqstm1 protein, mouse