ARNT Inhibits H5N1 Influenza A Virus Replication by Interacting with the PA Protein

Viruses. 2022 Jun 21;14(7):1347. doi: 10.3390/v14071347.

Abstract

Increasing evidence suggests that the polymerase acidic (PA) protein of influenza A viruses plays an important role in viral replication and pathogenicity. However, information regarding the interaction(s) of host factors with PA is scarce. By using a yeast two-hybrid screen, we identified a novel host factor, aryl hydrocarbon receptor nuclear translocator (ARNT), that interacts with the PA protein of the H5N1 virus. The interaction between PA and human ARNT was confirmed by co-immunoprecipitation and immunofluorescence microscopy. Moreover, overexpression of ARNT downregulated the polymerase activity and inhibited virus propagation, whereas knockdown of ARNT significantly increased the polymerase activity and virus replication. Mechanistically, overexpression of ARNT resulted in the accumulation of PA protein in the nucleus and inhibited both the replication and transcription of the viral genome. Interaction domain mapping revealed that the bHLH/PAS domain of ARNT mainly interacted with the C-terminal domain of PA. Together, our results demonstrate that ARNT inhibits the replication of the H5N1 virus and could be a target for the development of therapeutic strategies against H5N1 influenza viruses.

Keywords: ARNT; H5N1 influenza A virus; PA; interacting; replication.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aryl Hydrocarbon Receptor Nuclear Translocator / metabolism
  • Humans
  • Influenza A Virus, H5N1 Subtype*
  • Influenza A virus*
  • Influenza, Human*
  • RNA-Dependent RNA Polymerase / metabolism
  • Virus Replication / genetics

Substances

  • ARNT protein, human
  • Aryl Hydrocarbon Receptor Nuclear Translocator
  • RNA-Dependent RNA Polymerase

Grants and funding

This work was supported by the Zhejiang Provincial Natural Science Foundation of China (LY22C180002 for H.F. and LQ22C180003 for L.W.), the “Pioneer” and “Leading Goose” R&D Program of Zhejiang (2022C02031), the Science Foundation of Zhejiang Sci-Tech University (20042220-Y), the Fundamental Research Funds of Zhejiang Sci-Tech University (2021Q035), and the Open Fund of Shaoxing Academy of Biomedicine of Zhejiang Sci-Tech University under Grant No. SXAB202019.