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Characterization of avian influenza virus attachment patterns to human and pig tissues

Wild birds of Anseriformes and Charadriiformes are natural reservoirs of influenza A viruses (IAVs). Occasionally, IAVs transmit and adapt to mammalian hosts, and are maintained as epidemic strains in their new hosts. Viral adaptions to mammalian hosts include altered receptor preference of host epi...

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Autores principales: Eriksson, Per, Lindskog, Cecilia, Engholm, Ebbe, Blixt, Ola, Waldenström, Jonas, Munster, Vincent, Lundkvist, Åke, Olsen, Björn, Jourdain, Elsa, Ellström, Patrik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6093914/
https://www.ncbi.nlm.nih.gov/pubmed/30111851
http://dx.doi.org/10.1038/s41598-018-29578-1
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author Eriksson, Per
Lindskog, Cecilia
Engholm, Ebbe
Blixt, Ola
Waldenström, Jonas
Munster, Vincent
Lundkvist, Åke
Olsen, Björn
Jourdain, Elsa
Ellström, Patrik
author_facet Eriksson, Per
Lindskog, Cecilia
Engholm, Ebbe
Blixt, Ola
Waldenström, Jonas
Munster, Vincent
Lundkvist, Åke
Olsen, Björn
Jourdain, Elsa
Ellström, Patrik
author_sort Eriksson, Per
collection PubMed
description Wild birds of Anseriformes and Charadriiformes are natural reservoirs of influenza A viruses (IAVs). Occasionally, IAVs transmit and adapt to mammalian hosts, and are maintained as epidemic strains in their new hosts. Viral adaptions to mammalian hosts include altered receptor preference of host epithelial sialylated oligosaccharides from terminal α2,3-linked sialic acid (SA) towards α2,6-linked SA. However, α2,3-linked SA has been found in human respiratory tract epithelium, and human infections by avian IAVs (AIVs) have been reported. To further explore the attachment properties of AIVs, four AIVs of different subtypes were investigated on human and pig tissues using virus histochemistry. Additionally, glycan array analysis was performed for further characterization of IAVs’ receptor structure tropism. Generally, AIV attachment was more abundant to human tissues than to pig tissues. The attachment pattern was very strong to human conjunctiva and upper respiratory tract, but variable to the lower respiratory tract. AIVs mainly attached to α2,3-linked SA, but also to combinations of α2,3- and α2,6-linked SA. The low attachment of these AIV isolates to pig tissues, but high attachment to human tissues, addresses the question whether AIVs in general require passage through pigs to obtain adaptions towards mammalian receptor structures.
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spelling pubmed-60939142018-08-20 Characterization of avian influenza virus attachment patterns to human and pig tissues Eriksson, Per Lindskog, Cecilia Engholm, Ebbe Blixt, Ola Waldenström, Jonas Munster, Vincent Lundkvist, Åke Olsen, Björn Jourdain, Elsa Ellström, Patrik Sci Rep Article Wild birds of Anseriformes and Charadriiformes are natural reservoirs of influenza A viruses (IAVs). Occasionally, IAVs transmit and adapt to mammalian hosts, and are maintained as epidemic strains in their new hosts. Viral adaptions to mammalian hosts include altered receptor preference of host epithelial sialylated oligosaccharides from terminal α2,3-linked sialic acid (SA) towards α2,6-linked SA. However, α2,3-linked SA has been found in human respiratory tract epithelium, and human infections by avian IAVs (AIVs) have been reported. To further explore the attachment properties of AIVs, four AIVs of different subtypes were investigated on human and pig tissues using virus histochemistry. Additionally, glycan array analysis was performed for further characterization of IAVs’ receptor structure tropism. Generally, AIV attachment was more abundant to human tissues than to pig tissues. The attachment pattern was very strong to human conjunctiva and upper respiratory tract, but variable to the lower respiratory tract. AIVs mainly attached to α2,3-linked SA, but also to combinations of α2,3- and α2,6-linked SA. The low attachment of these AIV isolates to pig tissues, but high attachment to human tissues, addresses the question whether AIVs in general require passage through pigs to obtain adaptions towards mammalian receptor structures. Nature Publishing Group UK 2018-08-15 /pmc/articles/PMC6093914/ /pubmed/30111851 http://dx.doi.org/10.1038/s41598-018-29578-1 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Eriksson, Per
Lindskog, Cecilia
Engholm, Ebbe
Blixt, Ola
Waldenström, Jonas
Munster, Vincent
Lundkvist, Åke
Olsen, Björn
Jourdain, Elsa
Ellström, Patrik
Characterization of avian influenza virus attachment patterns to human and pig tissues
title Characterization of avian influenza virus attachment patterns to human and pig tissues
title_full Characterization of avian influenza virus attachment patterns to human and pig tissues
title_fullStr Characterization of avian influenza virus attachment patterns to human and pig tissues
title_full_unstemmed Characterization of avian influenza virus attachment patterns to human and pig tissues
title_short Characterization of avian influenza virus attachment patterns to human and pig tissues
title_sort characterization of avian influenza virus attachment patterns to human and pig tissues
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6093914/
https://www.ncbi.nlm.nih.gov/pubmed/30111851
http://dx.doi.org/10.1038/s41598-018-29578-1
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