MHC class II proteins mediate sialic acid independent entry of human and avian H2N2 influenza A viruses

Nat Microbiol. 2024 Oct;9(10):2626-2641. doi: 10.1038/s41564-024-01771-1. Epub 2024 Jul 15.

Abstract

Influenza A viruses (IAV) pose substantial burden on human and animal health. Avian, swine and human IAV bind sialic acid on host glycans as receptor, whereas some bat IAV require MHC class II complexes for cell entry. It is unknown how this difference evolved and whether dual receptor specificity is possible. Here we show that human H2N2 IAV and related avian H2N2 possess dual receptor specificity in cell lines and primary human airway cultures. Using sialylation-deficient cells, we reveal that entry via MHC class II is independent of sialic acid. We find that MHC class II from humans, pigs, ducks, swans and chickens but not bats can mediate H2 IAV entry and that this is conserved in Eurasian avian H2. Our results demonstrate that IAV can possess dual receptor specificity for sialic acid and MHC class II, and suggest a role for MHC class II-dependent entry in zoonotic IAV infections.

MeSH terms

  • Animals
  • Birds / virology
  • Cell Line
  • Chickens / virology
  • Chiroptera / virology
  • Ducks / virology
  • Histocompatibility Antigens Class II* / metabolism
  • Humans
  • Influenza A Virus, H2N2 Subtype* / genetics
  • Influenza A Virus, H2N2 Subtype* / immunology
  • Influenza A Virus, H2N2 Subtype* / metabolism
  • Influenza in Birds* / immunology
  • Influenza in Birds* / metabolism
  • Influenza in Birds* / virology
  • Influenza, Human* / immunology
  • Influenza, Human* / metabolism
  • Influenza, Human* / virology
  • N-Acetylneuraminic Acid* / metabolism
  • Receptors, Virus* / genetics
  • Receptors, Virus* / metabolism
  • Swine
  • Virus Internalization*

Substances

  • N-Acetylneuraminic Acid
  • Histocompatibility Antigens Class II
  • Receptors, Virus