Evolution of a concept: From accessory protein to key virulence factor, the case of HIV-1 Vpr

Biochem Pharmacol. 2020 Oct:180:114128. doi: 10.1016/j.bcp.2020.114128. Epub 2020 Jun 30.

Abstract

Back in 1989 some studies have shown that the viral protein Vpr was dispensable for HIV-1 replication in vitro. From then the concept of accessory or auxiliary protein for Vpr has emerged and it is still used to date. However, Vpr soon appeared to be very important for in vivo virus spread and pathogenesis. Vpr has been involved in many biological functions including regulation of reverse transcriptase activity, the nuclear import of the pre-integration complex (PIC), HIV-1 transcription, gene splicing, apoptosis and in cell cycle arrest. Thus, we might rather consider Vpr as a true virulence factor instead of just an accessory factor. At present, Vpr can be regarded as a potential and promising target in different strategies aiming to fight infected cells including latently infected cells.

Keywords: HIV-1; Virulence factor; Vpr.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Amino Acid Sequence
  • Apoptosis / genetics
  • Cell Cycle / genetics
  • Disease Progression
  • HIV Infections / immunology
  • HIV Infections / virology
  • Humans
  • Mutagenesis, Site-Directed
  • Polymorphism, Genetic*
  • T-Lymphocytes / immunology
  • T-Lymphocytes / pathology
  • T-Lymphocytes / virology
  • Transcription, Genetic*
  • Virulence Factors / genetics*
  • Virulence Factors / physiology
  • vpr Gene Products, Human Immunodeficiency Virus / genetics*
  • vpr Gene Products, Human Immunodeficiency Virus / physiology

Substances

  • Virulence Factors
  • vpr Gene Products, Human Immunodeficiency Virus
  • vpr protein, Human immunodeficiency virus 1