BRD4 inhibition exerts anti-viral activity through DNA damage-dependent innate immune responses

PLoS Pathog. 2020 Mar 24;16(3):e1008429. doi: 10.1371/journal.ppat.1008429. eCollection 2020 Mar.

Abstract

Chromatin dynamics regulated by epigenetic modification is crucial in genome stability and gene expression. Various epigenetic mechanisms have been identified in the pathogenesis of human diseases. Here, we examined the effects of ten epigenetic agents on pseudorabies virus (PRV) infection by using GFP-reporter assays. Inhibitors of bromodomain protein 4 (BRD4), which receives much more attention in cancer than viral infection, was found to exhibit substantial anti-viral activity against PRV as well as a range of DNA and RNA viruses. We further demonstrated that BRD4 inhibition boosted a robust innate immune response. BRD4 inhibition also de-compacted chromatin structure and induced the DNA damage response, thereby triggering the activation of cGAS-mediated innate immunity and increasing host resistance to viral infection both in vitro and in vivo. Mechanistically, the inhibitory effect of BRD4 inhibition on viral infection was mainly attributed to the attenuation of viral attachment. Our findings reveal a unique mechanism through which BRD4 inhibition restrains viral infection and points to its potent therapeutic value for viral infectious diseases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • A549 Cells
  • Animals
  • Cell Cycle Proteins / immunology*
  • Chlorocebus aethiops
  • DNA Damage / immunology*
  • DNA Virus Infections / immunology
  • DNA Viruses / immunology*
  • Dogs
  • Female
  • HEK293 Cells
  • HeLa Cells
  • Humans
  • Immunity, Innate*
  • Madin Darby Canine Kidney Cells
  • Mice
  • Mice, Inbred BALB C
  • NIH 3T3 Cells
  • Nuclear Proteins / immunology*
  • RAW 264.7 Cells
  • RNA Virus Infections / immunology
  • RNA Viruses / immunology*
  • Swine
  • Transcription Factors / immunology*
  • Vero Cells

Substances

  • BRD4 protein, human
  • Brd4 protein, mouse
  • Cell Cycle Proteins
  • Nuclear Proteins
  • Transcription Factors

Grants and funding

This work was supported by (2016ZX08006001-006) the Ministry of Agriculture and Rural Affairs of China (http://www.moa.gov.cn/) for GYY and by the (31502031) National Natural Science Foundation of China (http://www.nsfc.gov.cn/) for BBC. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.