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Limited Antigenic Diversity in Contemporary H7 Avian-Origin Influenza A Viruses from North America
Subtype H7 avian–origin influenza A viruses (AIVs) have caused at least 500 confirmed human infections since 2003 and culling of >75 million birds in recent years. Here we antigenically and genetically characterized 93 AIV isolates from North America (85 from migratory waterfowl [1976–2010], 7 fr...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4746648/ https://www.ncbi.nlm.nih.gov/pubmed/26858078 http://dx.doi.org/10.1038/srep20688 |
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author | Xu, Yifei Bailey, Elizabeth Spackman, Erica Li, Tao Wang, Hui Long, Li-Ping Baroch, John A. Cunningham, Fred L. Lin, Xiaoxu Jarman, Richard G. DeLiberto, Thomas J. Wan, Xiu-Feng |
author_facet | Xu, Yifei Bailey, Elizabeth Spackman, Erica Li, Tao Wang, Hui Long, Li-Ping Baroch, John A. Cunningham, Fred L. Lin, Xiaoxu Jarman, Richard G. DeLiberto, Thomas J. Wan, Xiu-Feng |
author_sort | Xu, Yifei |
collection | PubMed |
description | Subtype H7 avian–origin influenza A viruses (AIVs) have caused at least 500 confirmed human infections since 2003 and culling of >75 million birds in recent years. Here we antigenically and genetically characterized 93 AIV isolates from North America (85 from migratory waterfowl [1976–2010], 7 from domestic poultry [1971–2012], and 1 from a seal [1980]). The hemagglutinin gene of these H7 viruses are separated from those from Eurasia. Gradual accumulation of nucleotide and amino acid substitutions was observed in the hemagglutinin of H7 AIVs from waterfowl and domestic poultry. Genotype characterization suggested that H7 AIVs in wild birds form diverse and transient internal gene constellations. Serologic analyses showed that the 93 isolates cross-reacted with each other to different extents. Antigenic cartography showed that the average antigenic distance among them was 1.14 units (standard deviation [SD], 0.57 unit) and that antigenic diversity among the H7 isolates we tested was limited. Our results suggest that the continuous genetic evolution has not led to significant antigenic diversity for H7 AIVs from North America. These findings add to our understanding of the natural history of IAVs and will inform public health decision-making regarding the threat these viruses pose to humans and poultry. |
format | Online Article Text |
id | pubmed-4746648 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47466482016-02-17 Limited Antigenic Diversity in Contemporary H7 Avian-Origin Influenza A Viruses from North America Xu, Yifei Bailey, Elizabeth Spackman, Erica Li, Tao Wang, Hui Long, Li-Ping Baroch, John A. Cunningham, Fred L. Lin, Xiaoxu Jarman, Richard G. DeLiberto, Thomas J. Wan, Xiu-Feng Sci Rep Article Subtype H7 avian–origin influenza A viruses (AIVs) have caused at least 500 confirmed human infections since 2003 and culling of >75 million birds in recent years. Here we antigenically and genetically characterized 93 AIV isolates from North America (85 from migratory waterfowl [1976–2010], 7 from domestic poultry [1971–2012], and 1 from a seal [1980]). The hemagglutinin gene of these H7 viruses are separated from those from Eurasia. Gradual accumulation of nucleotide and amino acid substitutions was observed in the hemagglutinin of H7 AIVs from waterfowl and domestic poultry. Genotype characterization suggested that H7 AIVs in wild birds form diverse and transient internal gene constellations. Serologic analyses showed that the 93 isolates cross-reacted with each other to different extents. Antigenic cartography showed that the average antigenic distance among them was 1.14 units (standard deviation [SD], 0.57 unit) and that antigenic diversity among the H7 isolates we tested was limited. Our results suggest that the continuous genetic evolution has not led to significant antigenic diversity for H7 AIVs from North America. These findings add to our understanding of the natural history of IAVs and will inform public health decision-making regarding the threat these viruses pose to humans and poultry. Nature Publishing Group 2016-02-09 /pmc/articles/PMC4746648/ /pubmed/26858078 http://dx.doi.org/10.1038/srep20688 Text en Copyright © 2016, Macmillan Publishers Limited 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 Xu, Yifei Bailey, Elizabeth Spackman, Erica Li, Tao Wang, Hui Long, Li-Ping Baroch, John A. Cunningham, Fred L. Lin, Xiaoxu Jarman, Richard G. DeLiberto, Thomas J. Wan, Xiu-Feng Limited Antigenic Diversity in Contemporary H7 Avian-Origin Influenza A Viruses from North America |
title | Limited Antigenic Diversity in Contemporary H7 Avian-Origin Influenza A Viruses from North America |
title_full | Limited Antigenic Diversity in Contemporary H7 Avian-Origin Influenza A Viruses from North America |
title_fullStr | Limited Antigenic Diversity in Contemporary H7 Avian-Origin Influenza A Viruses from North America |
title_full_unstemmed | Limited Antigenic Diversity in Contemporary H7 Avian-Origin Influenza A Viruses from North America |
title_short | Limited Antigenic Diversity in Contemporary H7 Avian-Origin Influenza A Viruses from North America |
title_sort | limited antigenic diversity in contemporary h7 avian-origin influenza a viruses from north america |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4746648/ https://www.ncbi.nlm.nih.gov/pubmed/26858078 http://dx.doi.org/10.1038/srep20688 |
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