A hnRNPA2B1 agonist effectively inhibits HBV and SARS-CoV-2 omicron in vivo

Protein Cell. 2022 Jul 15;14(1):37-50. doi: 10.1093/procel/pwac027. eCollection 2023 Jan.

Abstract

The twenty-first century has already recorded more than ten major epidemics or pandemics of viral disease, including the devastating COVID-19. Novel effective antivirals with broad-spectrum coverage are urgently needed. Herein, we reported a novel broad-spectrum antiviral compound PAC5. Oral administration of PAC5 eliminated HBV cccDNA and reduced the large antigen load in distinct mouse models of HBV infection. Strikingly, oral administration of PAC5 in a hamster model of SARS-CoV-2 omicron (BA.1) infection significantly decreases viral loads and attenuates lung inflammation. Mechanistically, PAC5 binds to a pocket near Asp49 in the RNA recognition motif of hnRNPA2B1. PAC5-bound hnRNPA2B1 is extensively activated and translocated to the cytoplasm where it initiates the TBK1-IRF3 pathway, leading to the production of type I IFNs with antiviral activity. Our results indicate that PAC5 is a novel small-molecule agonist of hnRNPA2B1, which may have a role in dealing with emerging infectious diseases now and in the future.

Keywords: HBV; PAC5; SARS-CoV-2 omicron; TBK1-IRF3 pathway; hnRNPA2B1; type I IFNs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antiviral Agents* / pharmacology
  • COVID-19
  • Hepatitis B virus*
  • Heterogeneous-Nuclear Ribonucleoprotein Group A-B* / antagonists & inhibitors
  • Interferon Type I / metabolism
  • Mice
  • SARS-CoV-2* / drug effects

Substances

  • Antiviral Agents
  • Interferon Type I
  • hnRNP A2
  • Heterogeneous-Nuclear Ribonucleoprotein Group A-B