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Ferrets exclusively synthesize Neu5Ac and express naturally humanized influenza A virus receptors
Mammals express the sialic acids N-acetylneuraminic acid (Neu5Ac) and N-glycolylneuraminic acid (Neu5Gc) on cell surfaces, where they act as receptors for pathogens, including influenza A virus (IAV). Neu5Gc is synthesized from Neu5Ac by the enzyme cytidine monophosphate-N-acetylneuraminic acid hydr...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Pub. Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4351649/ https://www.ncbi.nlm.nih.gov/pubmed/25517696 http://dx.doi.org/10.1038/ncomms6750 |
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author | Ng, Preston S.K. Böhm, Raphael Hartley-Tassell, Lauren E. Steen, Jason A. Wang, Hui Lukowski, Samuel W. Hawthorne, Paula L. Trezise, Ann E.O. Coloe, Peter J. Grimmond, Sean M. Haselhorst, Thomas von Itzstein, Mark Paton, Adrienne W. Paton, James C. Jennings, Michael P. |
author_facet | Ng, Preston S.K. Böhm, Raphael Hartley-Tassell, Lauren E. Steen, Jason A. Wang, Hui Lukowski, Samuel W. Hawthorne, Paula L. Trezise, Ann E.O. Coloe, Peter J. Grimmond, Sean M. Haselhorst, Thomas von Itzstein, Mark Paton, Adrienne W. Paton, James C. Jennings, Michael P. |
author_sort | Ng, Preston S.K. |
collection | PubMed |
description | Mammals express the sialic acids N-acetylneuraminic acid (Neu5Ac) and N-glycolylneuraminic acid (Neu5Gc) on cell surfaces, where they act as receptors for pathogens, including influenza A virus (IAV). Neu5Gc is synthesized from Neu5Ac by the enzyme cytidine monophosphate-N-acetylneuraminic acid hydroxylase (CMAH). In humans, this enzyme is inactive and only Neu5Ac is produced. Ferrets are susceptible to human-adapted IAV strains and have been the dominant animal model for IAV studies. Here we show that ferrets, like humans, do not synthesize Neu5Gc. Genomic analysis reveals an ancient, nine-exon deletion in the ferret CMAH gene that is shared by the Pinnipedia and Musteloidia members of the Carnivora. Interactions between two human strains of IAV with the sialyllactose receptor (sialic acid—α2,6Gal) confirm that the type of terminal sialic acid contributes significantly to IAV receptor specificity. Our results indicate that exclusive expression of Neu5Ac contributes to the susceptibility of ferrets to human-adapted IAV strains. |
format | Online Article Text |
id | pubmed-4351649 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Pub. Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-43516492015-03-19 Ferrets exclusively synthesize Neu5Ac and express naturally humanized influenza A virus receptors Ng, Preston S.K. Böhm, Raphael Hartley-Tassell, Lauren E. Steen, Jason A. Wang, Hui Lukowski, Samuel W. Hawthorne, Paula L. Trezise, Ann E.O. Coloe, Peter J. Grimmond, Sean M. Haselhorst, Thomas von Itzstein, Mark Paton, Adrienne W. Paton, James C. Jennings, Michael P. Nat Commun Article Mammals express the sialic acids N-acetylneuraminic acid (Neu5Ac) and N-glycolylneuraminic acid (Neu5Gc) on cell surfaces, where they act as receptors for pathogens, including influenza A virus (IAV). Neu5Gc is synthesized from Neu5Ac by the enzyme cytidine monophosphate-N-acetylneuraminic acid hydroxylase (CMAH). In humans, this enzyme is inactive and only Neu5Ac is produced. Ferrets are susceptible to human-adapted IAV strains and have been the dominant animal model for IAV studies. Here we show that ferrets, like humans, do not synthesize Neu5Gc. Genomic analysis reveals an ancient, nine-exon deletion in the ferret CMAH gene that is shared by the Pinnipedia and Musteloidia members of the Carnivora. Interactions between two human strains of IAV with the sialyllactose receptor (sialic acid—α2,6Gal) confirm that the type of terminal sialic acid contributes significantly to IAV receptor specificity. Our results indicate that exclusive expression of Neu5Ac contributes to the susceptibility of ferrets to human-adapted IAV strains. Nature Pub. Group 2014-12-17 /pmc/articles/PMC4351649/ /pubmed/25517696 http://dx.doi.org/10.1038/ncomms6750 Text en Copyright © 2014, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Ng, Preston S.K. Böhm, Raphael Hartley-Tassell, Lauren E. Steen, Jason A. Wang, Hui Lukowski, Samuel W. Hawthorne, Paula L. Trezise, Ann E.O. Coloe, Peter J. Grimmond, Sean M. Haselhorst, Thomas von Itzstein, Mark Paton, Adrienne W. Paton, James C. Jennings, Michael P. Ferrets exclusively synthesize Neu5Ac and express naturally humanized influenza A virus receptors |
title | Ferrets exclusively synthesize Neu5Ac and express naturally humanized influenza A virus receptors |
title_full | Ferrets exclusively synthesize Neu5Ac and express naturally humanized influenza A virus receptors |
title_fullStr | Ferrets exclusively synthesize Neu5Ac and express naturally humanized influenza A virus receptors |
title_full_unstemmed | Ferrets exclusively synthesize Neu5Ac and express naturally humanized influenza A virus receptors |
title_short | Ferrets exclusively synthesize Neu5Ac and express naturally humanized influenza A virus receptors |
title_sort | ferrets exclusively synthesize neu5ac and express naturally humanized influenza a virus receptors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4351649/ https://www.ncbi.nlm.nih.gov/pubmed/25517696 http://dx.doi.org/10.1038/ncomms6750 |
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