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Multiple amino acid substitutions involved in the adaption of three avian-origin H7N9 influenza viruses in mice

BACKGROUND: Avian influenza A H7N9 virus has caused five outbreak waves of human infections in China since 2013 and posed a dual challenge to public health and poultry industry. The number of reported H7N9 virus human cases confirmed by laboratory has surpassed that of H5N1 virus. However, the mecha...

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Autores principales: Qin, Jianru, Peng, Ouyang, Shen, Xiaoting, Gong, Lang, Xue, Chunyi, Cao, Yongchang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6323857/
https://www.ncbi.nlm.nih.gov/pubmed/30621708
http://dx.doi.org/10.1186/s12985-018-1109-1
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author Qin, Jianru
Peng, Ouyang
Shen, Xiaoting
Gong, Lang
Xue, Chunyi
Cao, Yongchang
author_facet Qin, Jianru
Peng, Ouyang
Shen, Xiaoting
Gong, Lang
Xue, Chunyi
Cao, Yongchang
author_sort Qin, Jianru
collection PubMed
description BACKGROUND: Avian influenza A H7N9 virus has caused five outbreak waves of human infections in China since 2013 and posed a dual challenge to public health and poultry industry. The number of reported H7N9 virus human cases confirmed by laboratory has surpassed that of H5N1 virus. However, the mechanism for how H7N9 influenza virus overcomes host range barrier has not been clearly understood. METHODS: To generate mouse-adapted H7N9 influenza viruses, we passaged three avian-origin H7N9 viruses in mice by lung-to-lung passages independently. Then, the characteristics between the parental and mouse-adapted H7N9 viruses was compared in the following aspects, including virulence in mice, tropism of different tissues, replication in MDCK cells and molecular mutations. RESULTS: After ten passages in mice, MLD(50) of the H7N9 viruses reduced >750-3,160,000 folds, and virus titers in MDCK cells increased 10-200 folds at 48 hours post-inoculation. Moreover, the mouse-adapted H7N9 viruses showed more expanded tissue tropism and more serious lung pathological lesions in mice. Further analysis of the amino acids changes revealed 10 amino acid substitutions located in PB2 (E627K), PB1 (W215R and D638G), PA (T97I), HA (H3 numbering: R220G, L226S, G279R and G493R) and NA (P3Q and R134I) proteins. Moreover, PB2 E627K substitution was shared by the three mouse-adapted viruses (two viruses belong to YRD lineage and one virus belongs to PRD lineage), and PA T97A substitution was shared by two mouse-adapted viruses (belong to YRD lineage). CONCLUSIONS: Our result indicated that the virulence in mice and virus titer in MDCK cells of H7N9 viruses significantly increased after adapted in mouse model. PB2 E627K and PA T97A substitutions are vital in mouse adaption and should be monitored during epidemiological study of H7N9 virus. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12985-018-1109-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-63238572019-01-11 Multiple amino acid substitutions involved in the adaption of three avian-origin H7N9 influenza viruses in mice Qin, Jianru Peng, Ouyang Shen, Xiaoting Gong, Lang Xue, Chunyi Cao, Yongchang Virol J Research BACKGROUND: Avian influenza A H7N9 virus has caused five outbreak waves of human infections in China since 2013 and posed a dual challenge to public health and poultry industry. The number of reported H7N9 virus human cases confirmed by laboratory has surpassed that of H5N1 virus. However, the mechanism for how H7N9 influenza virus overcomes host range barrier has not been clearly understood. METHODS: To generate mouse-adapted H7N9 influenza viruses, we passaged three avian-origin H7N9 viruses in mice by lung-to-lung passages independently. Then, the characteristics between the parental and mouse-adapted H7N9 viruses was compared in the following aspects, including virulence in mice, tropism of different tissues, replication in MDCK cells and molecular mutations. RESULTS: After ten passages in mice, MLD(50) of the H7N9 viruses reduced >750-3,160,000 folds, and virus titers in MDCK cells increased 10-200 folds at 48 hours post-inoculation. Moreover, the mouse-adapted H7N9 viruses showed more expanded tissue tropism and more serious lung pathological lesions in mice. Further analysis of the amino acids changes revealed 10 amino acid substitutions located in PB2 (E627K), PB1 (W215R and D638G), PA (T97I), HA (H3 numbering: R220G, L226S, G279R and G493R) and NA (P3Q and R134I) proteins. Moreover, PB2 E627K substitution was shared by the three mouse-adapted viruses (two viruses belong to YRD lineage and one virus belongs to PRD lineage), and PA T97A substitution was shared by two mouse-adapted viruses (belong to YRD lineage). CONCLUSIONS: Our result indicated that the virulence in mice and virus titer in MDCK cells of H7N9 viruses significantly increased after adapted in mouse model. PB2 E627K and PA T97A substitutions are vital in mouse adaption and should be monitored during epidemiological study of H7N9 virus. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12985-018-1109-1) contains supplementary material, which is available to authorized users. BioMed Central 2019-01-08 /pmc/articles/PMC6323857/ /pubmed/30621708 http://dx.doi.org/10.1186/s12985-018-1109-1 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Qin, Jianru
Peng, Ouyang
Shen, Xiaoting
Gong, Lang
Xue, Chunyi
Cao, Yongchang
Multiple amino acid substitutions involved in the adaption of three avian-origin H7N9 influenza viruses in mice
title Multiple amino acid substitutions involved in the adaption of three avian-origin H7N9 influenza viruses in mice
title_full Multiple amino acid substitutions involved in the adaption of three avian-origin H7N9 influenza viruses in mice
title_fullStr Multiple amino acid substitutions involved in the adaption of three avian-origin H7N9 influenza viruses in mice
title_full_unstemmed Multiple amino acid substitutions involved in the adaption of three avian-origin H7N9 influenza viruses in mice
title_short Multiple amino acid substitutions involved in the adaption of three avian-origin H7N9 influenza viruses in mice
title_sort multiple amino acid substitutions involved in the adaption of three avian-origin h7n9 influenza viruses in mice
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6323857/
https://www.ncbi.nlm.nih.gov/pubmed/30621708
http://dx.doi.org/10.1186/s12985-018-1109-1
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