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Potential Pandemic of H7N9 Avian Influenza A Virus in Human
Since 2013, the H7N9 avian influenza A virus (AIV) has caused human infections and to the extent of now surpassing H5N1. This raises an alarm about the potential of H7N9 to become a pandemic problem. Our compilation of the amino acid changes required for AIVs to cross the species-barrier discovers 5...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6265602/ https://www.ncbi.nlm.nih.gov/pubmed/30533399 http://dx.doi.org/10.3389/fcimb.2018.00414 |
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author | Pu, Zhiqing Xiang, Dan Li, Xiaobing Luo, Tingting Shen, Xuejuan Murphy, Robert W. Liao, Ming Shen, Yongyi |
author_facet | Pu, Zhiqing Xiang, Dan Li, Xiaobing Luo, Tingting Shen, Xuejuan Murphy, Robert W. Liao, Ming Shen, Yongyi |
author_sort | Pu, Zhiqing |
collection | PubMed |
description | Since 2013, the H7N9 avian influenza A virus (AIV) has caused human infections and to the extent of now surpassing H5N1. This raises an alarm about the potential of H7N9 to become a pandemic problem. Our compilation of the amino acid changes required for AIVs to cross the species-barrier discovers 58 that have very high proportions in both the human- and avian-isolated H7N9 viruses. These changes correspond with sporadic human infections that continue to occur in regions of avian infections. Among the six internal viral genes, amino acid changes do not differ significantly between H9N2 and H7N9, except for V100A in PA, and K526R, D627K, and D701N in PB2. H9N2 AIVs provide internal genes to H7N9. Most of the amino acid changes in H7N9 appear to come directly from H9N2. Seventeen amino acid substitutions appear to have fixed quickly by the 5th wave. Among these, six amino acid sites in HA1 are receptor binding sites, and PB2-A588V was shown to promote the adaptation of AIVs to mammals. The accelerated fixation of mutations may promote the adaptation of H7N9 to human, but need further functional evidence. Although H7N9 AIVs still cannot efficiently transmit between humans, they have the genetic makeup associated with human infections. These viruses must be controlled in poultry to remove the threat of it becoming a human pandemic event. |
format | Online Article Text |
id | pubmed-6265602 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-62656022018-12-07 Potential Pandemic of H7N9 Avian Influenza A Virus in Human Pu, Zhiqing Xiang, Dan Li, Xiaobing Luo, Tingting Shen, Xuejuan Murphy, Robert W. Liao, Ming Shen, Yongyi Front Cell Infect Microbiol Cellular and Infection Microbiology Since 2013, the H7N9 avian influenza A virus (AIV) has caused human infections and to the extent of now surpassing H5N1. This raises an alarm about the potential of H7N9 to become a pandemic problem. Our compilation of the amino acid changes required for AIVs to cross the species-barrier discovers 58 that have very high proportions in both the human- and avian-isolated H7N9 viruses. These changes correspond with sporadic human infections that continue to occur in regions of avian infections. Among the six internal viral genes, amino acid changes do not differ significantly between H9N2 and H7N9, except for V100A in PA, and K526R, D627K, and D701N in PB2. H9N2 AIVs provide internal genes to H7N9. Most of the amino acid changes in H7N9 appear to come directly from H9N2. Seventeen amino acid substitutions appear to have fixed quickly by the 5th wave. Among these, six amino acid sites in HA1 are receptor binding sites, and PB2-A588V was shown to promote the adaptation of AIVs to mammals. The accelerated fixation of mutations may promote the adaptation of H7N9 to human, but need further functional evidence. Although H7N9 AIVs still cannot efficiently transmit between humans, they have the genetic makeup associated with human infections. These viruses must be controlled in poultry to remove the threat of it becoming a human pandemic event. Frontiers Media S.A. 2018-11-23 /pmc/articles/PMC6265602/ /pubmed/30533399 http://dx.doi.org/10.3389/fcimb.2018.00414 Text en Copyright © 2018 Pu, Xiang, Li, Luo, Shen, Murphy, Liao and Shen. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cellular and Infection Microbiology Pu, Zhiqing Xiang, Dan Li, Xiaobing Luo, Tingting Shen, Xuejuan Murphy, Robert W. Liao, Ming Shen, Yongyi Potential Pandemic of H7N9 Avian Influenza A Virus in Human |
title | Potential Pandemic of H7N9 Avian Influenza A Virus in Human |
title_full | Potential Pandemic of H7N9 Avian Influenza A Virus in Human |
title_fullStr | Potential Pandemic of H7N9 Avian Influenza A Virus in Human |
title_full_unstemmed | Potential Pandemic of H7N9 Avian Influenza A Virus in Human |
title_short | Potential Pandemic of H7N9 Avian Influenza A Virus in Human |
title_sort | potential pandemic of h7n9 avian influenza a virus in human |
topic | Cellular and Infection Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6265602/ https://www.ncbi.nlm.nih.gov/pubmed/30533399 http://dx.doi.org/10.3389/fcimb.2018.00414 |
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