Effect of Strain Variations on Lassa Virus Z Protein-Mediated Human RIG-I Inhibition

Viruses. 2020 Aug 19;12(9):907. doi: 10.3390/v12090907.

Abstract

Mammarenaviruses include several known human pathogens, such as the prototypic lymphocytic choriomeningitis virus (LCMV) that can cause neurological diseases and Lassa virus (LASV) that causes endemic hemorrhagic fever infection. LASV-infected patients show diverse clinical manifestations ranging from asymptomatic infection to hemorrhage, multi-organ failures and death, the mechanisms of which have not been well characterized. We have previously shown that the matrix protein Z of pathogenic arenaviruses, including LASV and LCMV, can strongly inhibit the ability of the innate immune protein RIG-I to suppress type I interferon (IFN-I) expression, which serves as a mechanism of viral immune evasion and virulence. Here, we show that Z proteins of diverse LASV isolates derived from rodents and humans have a high degree of sequence variations at their N- and C-terminal regions and produce variable degrees of inhibition of human RIG-I (hRIG-I) function in an established IFN-β promoter-driven luciferase (LUC) reporter assay. Additionally, we show that Z proteins of four known LCMV strains can also inhibit hRIG-I at variable degrees of efficiency. Collectively, our results confirm that Z proteins of pathogenic LASV and LCMV can inhibit hRIG-I and suggest that strain variations of the Z proteins can influence their efficiency to suppress host innate immunity that might contribute to viral virulence and disease heterogeneity.

Keywords: LCMV; Lassa virus; RIG-I; Z protein; arenavirus; immune evasion; innate immunity; sequence variations.

Publication types

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

MeSH terms

  • Amino Acid Motifs
  • Cell Line
  • DEAD Box Protein 58 / genetics
  • DEAD Box Protein 58 / immunology*
  • Host-Pathogen Interactions
  • Humans
  • Immunity, Innate
  • Interferon-beta / genetics
  • Interferon-beta / immunology
  • Lassa Fever / genetics
  • Lassa Fever / immunology*
  • Lassa Fever / virology*
  • Lassa virus / chemistry
  • Lassa virus / classification
  • Lassa virus / genetics
  • Lassa virus / immunology*
  • Lymphocytic choriomeningitis virus / chemistry
  • Lymphocytic choriomeningitis virus / classification
  • Lymphocytic choriomeningitis virus / genetics
  • Lymphocytic choriomeningitis virus / immunology
  • Receptors, Immunologic / genetics
  • Receptors, Immunologic / immunology*
  • Viral Proteins / chemistry
  • Viral Proteins / genetics
  • Viral Proteins / immunology*

Substances

  • Receptors, Immunologic
  • Viral Proteins
  • Interferon-beta
  • RIGI protein, human
  • DEAD Box Protein 58