A single mutation in Taiwanese H6N1 influenza hemagglutinin switches binding to human‐type receptors. Issue 9 (10th July 2017)

• Record Type: Journal Article
• Authors: de Vries, Robert P; Tzarum, Netanel; Peng, Wenjie; Thompson, Andrew J; Ambepitiya Wickramasinghe, Iresha N; de la Pena, Alba T Torrents; van Breemen, Marielle J; Bouwman, Kim M; Zhu, Xueyong; McBride, Ryan; Yu, Wenli; Sanders, Rogier W; Verheije, Monique H; Wilson, Ian A; Paulson, James C
• Is Part Of: EMBO molecular medicine. Volume 9:Issue 9(2017)
• Page Start: 1314
• Page End: 1325
• Publication Date: 2017-07-10
• Subjects: glycan array -- hemagglutinin -- influenza A virus -- sialic acid -- X‐ray crystallography; Molecular biology -- Periodicals; Medical genetics -- Periodicals; Pathology, Molecular -- Periodicals; 616.04205
• DOI: 10.15252/emmm.201707726
• Languages: English
• ISSNs: 1757-4676

Abstract

Abstract: In June 2013, the first case of human infection with an avian H6N1 virus was reported in a Taiwanese woman. Although this was a single non‐fatal case, the virus continues to circulate in Taiwanese poultry. As with any emerging avian virus that infects humans, there is concern that acquisition of human‐type receptor specificity could enable transmission in the human population. Despite mutations in the receptor‐binding pocket of the human H6N1 isolate, it has retained avian‐type (NeuAcα2‐3Gal) receptor specificity. However, we show here that a single nucleotide substitution, resulting in a change from Gly to Asp at position 225 (G225D), completely switches specificity to human‐type (NeuAcα2‐6Gal) receptors. Significantly, G225D H6 loses binding to chicken trachea epithelium and is now able to bind to human tracheal tissue. Structural analysis reveals that Asp225 directly interacts with the penultimate Gal of the human‐type receptor, stabilizing human receptor binding. Synopsis: To transmit between humans, zoonotic viruses need to acquire human‐type receptor specificity. Analyzing the effects of different amino acid mutations in the receptor binding site revealed that H6 HA only requires a single amino acid mutation to specifically adapt to human‐type receptor binding. G225D in H6 HA confers human‐type receptor binding. H6‐G225D lost binding to chicken and gained binding to human airway tissues. Structural analyses show classic human‐type receptor binding. H6 G225D still maintains low thermostability and is thus not yet fully adapted to transmit between humans. Abstract : To transmit between humans, zoonotic viruses need to acquire human‐type receptor specificity. Analyzing the effects of different amino acid mutations in the receptor binding site revealed that H6 HA only requires a single amino acid mutation to specifically adapt to human‐type receptor binding.