Evidence that an interaction between the respiratory syncytial virus F and G proteins at the distal ends of virus filaments mediates efficient multiple cycle infection

Virology. 2024 Mar:591:109985. doi: 10.1016/j.virol.2024.109985. Epub 2024 Jan 5.

Abstract

Evidence for a stable interaction between the respiratory syncytial virus (RSV) F and G proteins on the surface of virus filaments was provided using antibody immunoprecipitation studies on purified RSV particles, and by the in situ analysis on the surface of RSV-infected cells using the proximity ligation assay. Imaging of the F and G protein distribution on virus filaments suggested that this protein complex was localised at the distal ends of the virus filaments, and suggested that this protein complex played a direct role in mediating efficient localised cell-to-cell virus transmission. G protein expression was required for efficient localised cell-to-cell transmission of RSV in cell monolayers which provided evidence that this protein complex mediates efficient multiple cycle infection. Collectively, these data provide evidence that F and G proteins form a complex on the surface of RSV particles, and that a role for this protein complex in promoting virus transmission is suggested.

Keywords: F protein; G protein; RSV transmission; Respiratory syncytial virus; Virus assembly; Virus envelope.

MeSH terms

  • Antibodies, Viral
  • Cytoskeleton
  • GTP-Binding Proteins / metabolism
  • Humans
  • Protein Processing, Post-Translational
  • Respiratory Syncytial Virus Infections*
  • Respiratory Syncytial Virus Vaccines*
  • Respiratory Syncytial Virus, Human*
  • Viral Fusion Proteins / genetics

Substances

  • Viral Fusion Proteins
  • GTP-Binding Proteins
  • Respiratory Syncytial Virus Vaccines
  • Antibodies, Viral