African swine fever virus structural protein p54 is essential for the recruitment of envelope precursors to assembly sites

J Virol. 2004 Apr;78(8):4299-1313. doi: 10.1128/jvi.78.8.4299-4313.2004.

Abstract

The assembly of African swine fever virus (ASFV) at the cytoplasmic virus factories commences with the formation of precursor membranous structures, which are thought to be collapsed cisternal domains recruited from the surrounding endoplasmic reticulum (ER). This report analyzes the role in virus morphogenesis of the structural protein p54, a 25-kDa polypeptide encoded by the E183L gene that contains a putative transmembrane domain and localizes at the ER-derived envelope precursors. We show that protein p54 behaves in vitro and in infected cells as a type I membrane-anchored protein that forms disulfide-linked homodimers through its unique luminal cysteine. Moreover, p54 is targeted to the ER membranes when it is transiently expressed in transfected cells. Using a lethal conditional recombinant, vE183Li, we also demonstrate that the repression of p54 synthesis arrests virus morphogenesis at a very early stage, even prior to the formation of the precursor membranes. Under restrictive conditions, the virus factories appeared as discrete electron-lucent areas essentially free of viral structures. In contrast, outside the assembly sites, large amounts of aberrant zipper-like structures formed by the unprocessed core polyproteins pp220 and pp62 were produced in close association to ER cisternae. Altogether, these results indicate that the transmembrane structural protein p54 is critical for the recruitment and transformation of the ER membranes into the precursors of the viral envelope.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • African Swine Fever Virus / genetics
  • African Swine Fever Virus / physiology*
  • Animals
  • Base Sequence
  • COS Cells
  • Chlorocebus aethiops
  • DNA, Viral / genetics
  • Dimerization
  • Endoplasmic Reticulum / metabolism
  • Endoplasmic Reticulum / virology
  • Gene Expression
  • Gene Products, env / genetics
  • Gene Products, env / physiology*
  • Genes, Viral
  • Microscopy, Electron
  • Microsomes / metabolism
  • Microsomes / virology
  • Protein Precursors / genetics
  • Protein Precursors / physiology
  • Protein Processing, Post-Translational
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism
  • Transfection
  • Vero Cells
  • Viral Structural Proteins / chemistry
  • Viral Structural Proteins / genetics
  • Viral Structural Proteins / physiology*
  • Virus Assembly

Substances

  • DNA, Viral
  • Gene Products, env
  • Protein Precursors
  • Recombinant Proteins
  • Viral Structural Proteins
  • p54 protein, African swine fever virus