Rhabdoviruses, Antiviral Defense, and SUMO Pathway

Viruses. 2018 Dec 3;10(12):686. doi: 10.3390/v10120686.

Abstract

Small Ubiquitin-like MOdifier (SUMO) conjugation to proteins has essential roles in several processes including localization, stability, and function of several players implicated in intrinsic and innate immunity. In human, five paralogs of SUMO are known of which three are ubiquitously expressed (SUMO1, 2, and 3). Infection by rhabdoviruses triggers cellular responses through the activation of pattern recognition receptors, which leads to the production and secretion of interferon. This review will focus on the effects of the stable expression of the different SUMO paralogs or Ubc9 depletion on rhabdoviruses-induced interferon production and interferon signaling pathways as well as on the expression and functions of restriction factors conferring the resistance to rhabdoviruses.

Keywords: IFN; MxA; PKR; SUMO; interferon; rabies virus; vesicular stomatitis virus.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Humans
  • Immunity, Innate
  • Interferons / immunology
  • Mice
  • Myxovirus Resistance Proteins / genetics
  • Protein Binding
  • Rabies virus / immunology
  • Receptors, Pattern Recognition / immunology
  • Rhabdoviridae / immunology*
  • Rhabdoviridae Infections / immunology*
  • Signal Transduction*
  • Small Ubiquitin-Related Modifier Proteins / immunology
  • Small Ubiquitin-Related Modifier Proteins / metabolism*
  • Sumoylation
  • Ubiquitin / metabolism
  • Ubiquitin-Conjugating Enzymes / metabolism
  • Vesicular stomatitis Indiana virus / immunology
  • eIF-2 Kinase / genetics

Substances

  • MX1 protein, human
  • Myxovirus Resistance Proteins
  • Receptors, Pattern Recognition
  • Small Ubiquitin-Related Modifier Proteins
  • Ubiquitin
  • Interferons
  • Ubiquitin-Conjugating Enzymes
  • EIF2AK2 protein, human
  • eIF-2 Kinase
  • ubiquitin-conjugating enzyme UBC9