Cytomegalovirus protein m154 perturbs the adaptor protein-1 compartment mediating broad-spectrum immune evasion

Elife. 2020 Jan 13:9:e50803. doi: 10.7554/eLife.50803.

Abstract

Cytomegaloviruses (CMVs) are ubiquitous pathogens known to employ numerous immunoevasive strategies that significantly impair the ability of the immune system to eliminate the infected cells. Here, we report that the single mouse CMV (MCMV) protein, m154, downregulates multiple surface molecules involved in the activation and costimulation of the immune cells. We demonstrate that m154 uses its cytoplasmic tail motif, DD, to interfere with the adaptor protein-1 (AP-1) complex, implicated in intracellular protein sorting and packaging. As a consequence of the perturbed AP-1 sorting, m154 promotes lysosomal degradation of several proteins involved in T cell costimulation, thus impairing virus-specific CD8+ T cell response and virus control in vivo. Additionally, we show that HCMV infection similarly interferes with the AP-1 complex. Altogether, we identify the robust mechanism employed by single viral immunomodulatory protein targeting a broad spectrum of cell surface molecules involved in the antiviral immune response.

Keywords: CD8+ T cells; PVR, CD155; adaptor protein-1, AP-1; cytomegalovirus, CMV; immune evasion; immunology; infectious disease; inflammation; m154 protein; microbiology; virus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Protein Complex 1 / immunology*
  • Animals
  • Cell Line
  • Down-Regulation
  • Humans
  • Immune Evasion / immunology*
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Muromegalovirus / genetics
  • Muromegalovirus / physiology*
  • Viral Proteins / genetics
  • Viral Proteins / metabolism*

Substances

  • Adaptor Protein Complex 1
  • Membrane Proteins
  • Viral Proteins