Your browser doesn't support javascript.
loading
MHC class II proteins mediate sialic acid independent entry of human and avian H2N2 influenza A viruses.
Karakus, Umut; Sempere Borau, Milagros; Martínez-Barragán, Patricia; von Kempis, Josephine; Yildiz, Soner; Arroyo-Fernández, Laura M; Pohl, Marie O; Steiger, Julia A; Glas, Irina; Hunziker, Annika; García-Sastre, Adolfo; Stertz, Silke.
Afiliação
  • Karakus U; Institute of Medical Virology, University of Zurich, Zurich, Switzerland.
  • Sempere Borau M; Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Martínez-Barragán P; Global Health and Emerging Pathogens Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • von Kempis J; Institute of Medical Virology, University of Zurich, Zurich, Switzerland.
  • Yildiz S; Institute of Medical Virology, University of Zurich, Zurich, Switzerland.
  • Arroyo-Fernández LM; Institute of Medical Virology, University of Zurich, Zurich, Switzerland.
  • Pohl MO; Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Steiger JA; Global Health and Emerging Pathogens Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Glas I; Institute of Medical Virology, University of Zurich, Zurich, Switzerland.
  • Hunziker A; Institute of Medical Virology, University of Zurich, Zurich, Switzerland.
  • García-Sastre A; Institute of Medical Virology, University of Zurich, Zurich, Switzerland.
  • Stertz S; Institute of Medical Virology, University of Zurich, Zurich, Switzerland.
Nat Microbiol ; 9(10): 2626-2641, 2024 Oct.
Article em En | MEDLINE | ID: mdl-39009691
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Receptores Virais / Antígenos de Histocompatibilidade Classe II / Ácido N-Acetilneuramínico / Influenza Humana / Vírus da Influenza A Subtipo H2N2 / Internalização do Vírus / Influenza Aviária Limite: Animals / Humans Idioma: En Revista: Nat Microbiol / Nat. microbiol / Nature microbiology Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Suíça

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Receptores Virais / Antígenos de Histocompatibilidade Classe II / Ácido N-Acetilneuramínico / Influenza Humana / Vírus da Influenza A Subtipo H2N2 / Internalização do Vírus / Influenza Aviária Limite: Animals / Humans Idioma: En Revista: Nat Microbiol / Nat. microbiol / Nature microbiology Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Suíça