BFRF1 protein is involved in EBV-mediated autophagy manipulation

Microbes Infect. 2020 Nov-Dec;22(10):585-591. doi: 10.1016/j.micinf.2020.08.002. Epub 2020 Sep 1.

Abstract

Viral egress and autophagy are two mechanisms that seem to be strictly connected in Herpesviruses's biology. Several data suggest that the autophagic machinery facilitates the egress of viral capsids and thus the production of new infectious particles. In the Herpesvirus family, viral nuclear egress is controlled and organized by a well conserved group of proteins named Nuclear Egress Complex (NEC). In the case of EBV, NEC is composed by BFRF1 and BFLF2 proteins, although the alterations of the nuclear host cell architecture are mainly driven by BFRF1, a multifunctional viral protein anchored to the inner nuclear membrane of the host cell. BFRF1 shares a peculiar distribution with several nuclear components and with them it strictly interacts. In this study, we investigated the possible role of BFRF1 in manipulating autophagy, pathway that possibly originates from nucleus, regulating the interplay between autophagy and viral egress.

Keywords: Autophagy; BFRF1; EBV lytic cycle; LC3; Lamin B1; Nuclear egress.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Autophagy*
  • HEK293 Cells
  • Herpesvirus 4, Human / physiology*
  • Humans
  • Lamin Type B / metabolism
  • Membrane Proteins / metabolism*
  • Microtubule-Associated Proteins / metabolism
  • Nuclear Envelope / metabolism
  • Protein Binding
  • Viral Proteins / metabolism*
  • Virus Release
  • rab GTP-Binding Proteins / metabolism
  • rab7 GTP-Binding Proteins

Substances

  • BFRF1 protein, Human herpesvirus 4
  • Lamin Type B
  • MAP1LC3A protein, human
  • Membrane Proteins
  • Microtubule-Associated Proteins
  • Viral Proteins
  • rab7 GTP-Binding Proteins
  • rab GTP-Binding Proteins