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Epidemiology, evolution and transmission of human metapneumovirus in Guangzhou China, 2013–2017
Human metapneumovirus (hMPV), first identified in 2001, is a major viral respiratory pathogen that worldwide reported. Fundamental questions concerning the dynamics of viral evolution and transmission at both regional and global scales remain unanswered. In this study, we obtained 32 G gene and 51 F...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6773679/ https://www.ncbi.nlm.nih.gov/pubmed/31575919 http://dx.doi.org/10.1038/s41598-019-50340-8 |
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author | Yi, Lina Zou, Lirong Peng, Jingju Yu, Jianxiang Song, Yingchao Liang, Lijun Guo, Qianfang Kang, Min Ke, Changwen Song, Tie Lu, Jing Wu, Jie |
author_facet | Yi, Lina Zou, Lirong Peng, Jingju Yu, Jianxiang Song, Yingchao Liang, Lijun Guo, Qianfang Kang, Min Ke, Changwen Song, Tie Lu, Jing Wu, Jie |
author_sort | Yi, Lina |
collection | PubMed |
description | Human metapneumovirus (hMPV), first identified in 2001, is a major viral respiratory pathogen that worldwide reported. Fundamental questions concerning the dynamics of viral evolution and transmission at both regional and global scales remain unanswered. In this study, we obtained 32 G gene and 51 F gene sequences of hMPV in Guangzhou, China in 2013–2017. Temporal and spatial phylogenetic analyses were undertaken by incorporating publicly available hMPV G gene (978) and F gene (767) sequences. The phylogenetic results show different global distribution patterns of hMPV before 1990, 1990–2005, and 2006–2017. A sharply increasing hMPV positive rate (11%) was detected in Guangzhou 2017, mainly caused by the B1 lineage of hMPV. A close phylogenetic relation was observed between hMPV strains from China and Japan, suggesting frequent hMPV transmissions between these regions. These results provide new insights into hMPV evolution, transmission, and spatial distribution and highlight Asia as a new epicenter for viral transmission and novel variant seeding after the year 2005. Conducting molecular surveillance of hMPV in Asian countries is critical for understanding the global circulation of hMPV and future vaccine design. |
format | Online Article Text |
id | pubmed-6773679 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67736792019-10-04 Epidemiology, evolution and transmission of human metapneumovirus in Guangzhou China, 2013–2017 Yi, Lina Zou, Lirong Peng, Jingju Yu, Jianxiang Song, Yingchao Liang, Lijun Guo, Qianfang Kang, Min Ke, Changwen Song, Tie Lu, Jing Wu, Jie Sci Rep Article Human metapneumovirus (hMPV), first identified in 2001, is a major viral respiratory pathogen that worldwide reported. Fundamental questions concerning the dynamics of viral evolution and transmission at both regional and global scales remain unanswered. In this study, we obtained 32 G gene and 51 F gene sequences of hMPV in Guangzhou, China in 2013–2017. Temporal and spatial phylogenetic analyses were undertaken by incorporating publicly available hMPV G gene (978) and F gene (767) sequences. The phylogenetic results show different global distribution patterns of hMPV before 1990, 1990–2005, and 2006–2017. A sharply increasing hMPV positive rate (11%) was detected in Guangzhou 2017, mainly caused by the B1 lineage of hMPV. A close phylogenetic relation was observed between hMPV strains from China and Japan, suggesting frequent hMPV transmissions between these regions. These results provide new insights into hMPV evolution, transmission, and spatial distribution and highlight Asia as a new epicenter for viral transmission and novel variant seeding after the year 2005. Conducting molecular surveillance of hMPV in Asian countries is critical for understanding the global circulation of hMPV and future vaccine design. Nature Publishing Group UK 2019-10-01 /pmc/articles/PMC6773679/ /pubmed/31575919 http://dx.doi.org/10.1038/s41598-019-50340-8 Text en © The Author(s) 2019 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 Yi, Lina Zou, Lirong Peng, Jingju Yu, Jianxiang Song, Yingchao Liang, Lijun Guo, Qianfang Kang, Min Ke, Changwen Song, Tie Lu, Jing Wu, Jie Epidemiology, evolution and transmission of human metapneumovirus in Guangzhou China, 2013–2017 |
title | Epidemiology, evolution and transmission of human metapneumovirus in Guangzhou China, 2013–2017 |
title_full | Epidemiology, evolution and transmission of human metapneumovirus in Guangzhou China, 2013–2017 |
title_fullStr | Epidemiology, evolution and transmission of human metapneumovirus in Guangzhou China, 2013–2017 |
title_full_unstemmed | Epidemiology, evolution and transmission of human metapneumovirus in Guangzhou China, 2013–2017 |
title_short | Epidemiology, evolution and transmission of human metapneumovirus in Guangzhou China, 2013–2017 |
title_sort | epidemiology, evolution and transmission of human metapneumovirus in guangzhou china, 2013–2017 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6773679/ https://www.ncbi.nlm.nih.gov/pubmed/31575919 http://dx.doi.org/10.1038/s41598-019-50340-8 |
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