M protein is sufficient for assembly and release of Peste des petits ruminants virus-like particles

Microb Pathog. 2017 Jun:107:81-87. doi: 10.1016/j.micpath.2017.03.021. Epub 2017 Mar 19.

Abstract

Peste des petits ruminants virus (PPRV), belonging to paramyxoviruses, has six structure proteins (such as matrix protein (M), nucleocapsid proteins (N), fusion protein (F) and hemagglutinin protein (H)) and could cause high morbidity and mortality in sheep and goats. Although a vaccine strain of PPRV has been rescued and co-expression of M and N could yield PPRV-like particles, the roles of structure proteins in virion assembly and release have not been investigated in detail. In this study, plasmids carrying PPRV cDNA sequences encoding the N, M, H, and F proteins were expressed in Vero cells. The co-expression of all four proteins resulted in the release of virus-like particles (VLPs) with similar release efficiency to that of authentic virions. Moreover, the co-expression of M together with F also resulted in efficient VLPs release. In the absence of M protein, the expression of no combination of the other proteins resulted in particle release. In summary, a VLPs production system for PPRV has been established and M protein is necessary for promoting the assembly and release of VLPs, of which the predominant protein is M protein. Further study will be focused on the immunogenicity of the VLPs.

Keywords: Assembly; M protein; Peste des petits ruminants virus; Release; Virus-like particles.

MeSH terms

  • Animals
  • Antibodies, Viral
  • Chlorocebus aethiops / metabolism
  • Chlorocebus aethiops / physiology
  • DNA, Complementary
  • DNA, Viral
  • Hemagglutinins, Viral / metabolism
  • Hemagglutinins, Viral / physiology
  • Mice
  • Nucleocapsid Proteins / metabolism
  • Nucleocapsid Proteins / physiology
  • Peste-des-petits-ruminants virus / genetics
  • Peste-des-petits-ruminants virus / immunology
  • Peste-des-petits-ruminants virus / metabolism*
  • Peste-des-petits-ruminants virus / physiology*
  • Vero Cells / metabolism*
  • Viral Fusion Proteins / metabolism
  • Viral Fusion Proteins / physiology
  • Viral Matrix Proteins / metabolism*

Substances

  • Antibodies, Viral
  • DNA, Complementary
  • DNA, Viral
  • Hemagglutinins, Viral
  • Nucleocapsid Proteins
  • Viral Fusion Proteins
  • Viral Matrix Proteins