Expression of influenza A virus glycan receptor candidates in mallard, chicken, and tufted duck

Author:

Nilsson Jonas123,Eriksson Per45,Naguib Mahmoud M67,Jax Elinor8,Sihlbom Carina3,Olsson Britt-Marie3,Lundkvist Åke67,Olsen Björn45,Järhult Josef D45,Larson Göran12ORCID,Ellström Patrik45ORCID

Affiliation:

1. Department of Laboratory Medicine, University of Gothenburg , Sahlgrenska University Hospital, Vita Stråket 12, Gothenburg SE-413 45 , Sweden

2. Laboratory of Clinical Chemistry, Sahlgrenska University Hospital , Bruna Stråket 16, Gothenburg SE-413 45 , Sweden

3. Proteomics Core Facility, University of Gothenburg, Sahlgrenska Academy , Medicinaregatan 9E, Gothenburg SE-405 30 , Sweden

4. Zoonosis Science Center , Department of Medical Sciences, Husargatan 3, , Uppsala, SE-75185 , Sweden

5. Uppsala University , Department of Medical Sciences, Husargatan 3, , Uppsala, SE-75185 , Sweden

6. Zoonosis Science Center , Department of Medical Biochemistry and Microbiology, Husargatan 3, , Uppsala, SE-75237 , Sweden

7. Uppsala University , Department of Medical Biochemistry and Microbiology, Husargatan 3, , Uppsala, SE-75237 , Sweden

8. Department of Migration, Max Planck Institute of Animal Behavior , Am Obstberg 1, Radolfzell, Baden-Württemberg DE-78315 , Germany

Abstract

Abstract Influenza A virus (IAV) pandemics result from interspecies transmission events within the avian reservoir and further into mammals including humans. Receptor incompatibility due to differently expressed glycan structures between species has been suggested to limit zoonotic IAV transmission from the wild bird reservoir as well as between different bird species. Using glycoproteomics, we have studied the repertoires of expressed glycan structures with focus on putative sialic acid-containing glycan receptors for IAV in mallard, chicken and tufted duck; three bird species with different roles in the zoonotic ecology of IAV. The methodology used pinpoints specific glycan structures to specific glycosylation sites of identified glycoproteins and was also used to successfully discriminate α2-3- from α2-6-linked terminal sialic acids by careful analysis of oxonium ions released from glycopeptides in tandem MS/MS (MS2), and MS/MS/MS (MS3). Our analysis clearly demonstrated that all three bird species can produce complex N-glycans including α2-3-linked sialyl Lewis structures, as well as both N- and O- glycans terminated with both α2-3- and α2-6-linked Neu5Ac. We also found the recently identified putative IAV receptor structures, Man-6P N-glycopeptides, in all tissues of the three bird species. Furthermore, we found many similarities in the repertoires of expressed receptors both between the bird species investigated and to previously published data from pigs and humans. Our findings of sialylated glycan structures, previously anticipated to be mammalian specific, in all three bird species may have major implications for our understanding of the role of receptor incompatibility in interspecies transmission of IAV.

Funder

Swedish Research Council

Proteomics Core Facility

National core facility for Pandemic Preparedness

Publisher

Oxford University Press (OUP)

Subject

Biochemistry

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