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Highly Pathogenic Influenza A(H5Nx) Viruses with Altered H5 Receptor-Binding Specificity
Emergence and intercontinental spread of highly pathogenic avian influenza A(H5Nx) virus clade 2.3.4.4 is unprecedented. H5N8 and H5N2 viruses have caused major economic losses in the poultry industry in Europe and North America, and lethal human infections with H5N6 virus have occurred in Asia. Kno...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Centers for Disease Control and Prevention
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5324792/ https://www.ncbi.nlm.nih.gov/pubmed/27869615 http://dx.doi.org/10.3201/eid2302.161072 |
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author | Guo, Hongbo de Vries, Erik McBride, Ryan Dekkers, Jojanneke Peng, Wenjie Bouwman, Kim M. Nycholat, Corwin Verheije, M. Helene Paulson, James C. van Kuppeveld, Frank J.M. de Haan, Cornelis A.M. |
author_facet | Guo, Hongbo de Vries, Erik McBride, Ryan Dekkers, Jojanneke Peng, Wenjie Bouwman, Kim M. Nycholat, Corwin Verheije, M. Helene Paulson, James C. van Kuppeveld, Frank J.M. de Haan, Cornelis A.M. |
author_sort | Guo, Hongbo |
collection | PubMed |
description | Emergence and intercontinental spread of highly pathogenic avian influenza A(H5Nx) virus clade 2.3.4.4 is unprecedented. H5N8 and H5N2 viruses have caused major economic losses in the poultry industry in Europe and North America, and lethal human infections with H5N6 virus have occurred in Asia. Knowledge of the evolution of receptor-binding specificity of these viruses, which might affect host range, is urgently needed. We report that emergence of these viruses is accompanied by a change in receptor-binding specificity. In contrast to ancestral clade 2.3.4 H5 proteins, novel clade 2.3.4.4 H5 proteins bind to fucosylated sialosides because of substitutions K222Q and S227R, which are unique for highly pathogenic influenza virus H5 proteins. North American clade 2.3.4.4 virus isolates have retained only the K222Q substitution but still bind fucosylated sialosides. Altered receptor-binding specificity of virus clade 2.3.4.4 H5 proteins might have contributed to emergence and spread of H5Nx viruses. |
format | Online Article Text |
id | pubmed-5324792 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Centers for Disease Control and Prevention |
record_format | MEDLINE/PubMed |
spelling | pubmed-53247922017-02-24 Highly Pathogenic Influenza A(H5Nx) Viruses with Altered H5 Receptor-Binding Specificity Guo, Hongbo de Vries, Erik McBride, Ryan Dekkers, Jojanneke Peng, Wenjie Bouwman, Kim M. Nycholat, Corwin Verheije, M. Helene Paulson, James C. van Kuppeveld, Frank J.M. de Haan, Cornelis A.M. Emerg Infect Dis Research Emergence and intercontinental spread of highly pathogenic avian influenza A(H5Nx) virus clade 2.3.4.4 is unprecedented. H5N8 and H5N2 viruses have caused major economic losses in the poultry industry in Europe and North America, and lethal human infections with H5N6 virus have occurred in Asia. Knowledge of the evolution of receptor-binding specificity of these viruses, which might affect host range, is urgently needed. We report that emergence of these viruses is accompanied by a change in receptor-binding specificity. In contrast to ancestral clade 2.3.4 H5 proteins, novel clade 2.3.4.4 H5 proteins bind to fucosylated sialosides because of substitutions K222Q and S227R, which are unique for highly pathogenic influenza virus H5 proteins. North American clade 2.3.4.4 virus isolates have retained only the K222Q substitution but still bind fucosylated sialosides. Altered receptor-binding specificity of virus clade 2.3.4.4 H5 proteins might have contributed to emergence and spread of H5Nx viruses. Centers for Disease Control and Prevention 2017-02 /pmc/articles/PMC5324792/ /pubmed/27869615 http://dx.doi.org/10.3201/eid2302.161072 Text en https://creativecommons.org/licenses/by/4.0/This is a publication of the U.S. Government. This publication is in the public domain and is therefore without copyright. All text from this work may be reprinted freely. Use of these materials should be properly cited. |
spellingShingle | Research Guo, Hongbo de Vries, Erik McBride, Ryan Dekkers, Jojanneke Peng, Wenjie Bouwman, Kim M. Nycholat, Corwin Verheije, M. Helene Paulson, James C. van Kuppeveld, Frank J.M. de Haan, Cornelis A.M. Highly Pathogenic Influenza A(H5Nx) Viruses with Altered H5 Receptor-Binding Specificity |
title | Highly Pathogenic Influenza A(H5Nx) Viruses with Altered H5 Receptor-Binding Specificity |
title_full | Highly Pathogenic Influenza A(H5Nx) Viruses with Altered H5 Receptor-Binding Specificity |
title_fullStr | Highly Pathogenic Influenza A(H5Nx) Viruses with Altered H5 Receptor-Binding Specificity |
title_full_unstemmed | Highly Pathogenic Influenza A(H5Nx) Viruses with Altered H5 Receptor-Binding Specificity |
title_short | Highly Pathogenic Influenza A(H5Nx) Viruses with Altered H5 Receptor-Binding Specificity |
title_sort | highly pathogenic influenza a(h5nx) viruses with altered h5 receptor-binding specificity |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5324792/ https://www.ncbi.nlm.nih.gov/pubmed/27869615 http://dx.doi.org/10.3201/eid2302.161072 |
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