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Genetic diversity and molecular evolution of human respiratory syncytial virus A and B
Human respiratory syncytial viruses (RSVs) are classified into two major groups (A and B) based on antigenic differences in the G glycoprotein. To investigate circulating characteristics and phylodynamic history of RSV, we analyzed the genetic variability and evolutionary pattern of RSVs from 1977 t...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8217232/ https://www.ncbi.nlm.nih.gov/pubmed/34155268 http://dx.doi.org/10.1038/s41598-021-92435-1 |
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author | Yu, Jie-Mei Fu, Yuan-Hui Peng, Xiang-Lei Zheng, Yan-Peng He, Jin-Sheng |
author_facet | Yu, Jie-Mei Fu, Yuan-Hui Peng, Xiang-Lei Zheng, Yan-Peng He, Jin-Sheng |
author_sort | Yu, Jie-Mei |
collection | PubMed |
description | Human respiratory syncytial viruses (RSVs) are classified into two major groups (A and B) based on antigenic differences in the G glycoprotein. To investigate circulating characteristics and phylodynamic history of RSV, we analyzed the genetic variability and evolutionary pattern of RSVs from 1977 to 2019 in this study. The results revealed that there was no recombination event of intergroup. Single nucleotide polymorphisms (SNPs) were observed through the genome with the highest occurrence rate in the G gene. Five and six sites in G protein of RSV-A and RSV-B, respectively, were further identified with a strong positive selection. The mean evolutionary rates for RSV-A and -B were estimated to be 1.48 × 10(–3) and 1.92 × 10(–3) nucleotide substitutions/site/year, respectively. The Bayesian skyline plot showed a constant population size of RSV-A and a sharp expansion of population size of RSV-B since 2005, and an obvious decrease 5 years later, then became stable again. The total population size of RSVs showed a similar tendency to that of RSV-B. Time-scaled phylogeny suggested a temporal specificity of the RSV-genotypes. Monitoring nucleotide changes and analyzing evolution pattern for RSVs could give valuable insights for vaccine and therapy strategies against RSV infection. |
format | Online Article Text |
id | pubmed-8217232 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-82172322021-06-22 Genetic diversity and molecular evolution of human respiratory syncytial virus A and B Yu, Jie-Mei Fu, Yuan-Hui Peng, Xiang-Lei Zheng, Yan-Peng He, Jin-Sheng Sci Rep Article Human respiratory syncytial viruses (RSVs) are classified into two major groups (A and B) based on antigenic differences in the G glycoprotein. To investigate circulating characteristics and phylodynamic history of RSV, we analyzed the genetic variability and evolutionary pattern of RSVs from 1977 to 2019 in this study. The results revealed that there was no recombination event of intergroup. Single nucleotide polymorphisms (SNPs) were observed through the genome with the highest occurrence rate in the G gene. Five and six sites in G protein of RSV-A and RSV-B, respectively, were further identified with a strong positive selection. The mean evolutionary rates for RSV-A and -B were estimated to be 1.48 × 10(–3) and 1.92 × 10(–3) nucleotide substitutions/site/year, respectively. The Bayesian skyline plot showed a constant population size of RSV-A and a sharp expansion of population size of RSV-B since 2005, and an obvious decrease 5 years later, then became stable again. The total population size of RSVs showed a similar tendency to that of RSV-B. Time-scaled phylogeny suggested a temporal specificity of the RSV-genotypes. Monitoring nucleotide changes and analyzing evolution pattern for RSVs could give valuable insights for vaccine and therapy strategies against RSV infection. Nature Publishing Group UK 2021-06-21 /pmc/articles/PMC8217232/ /pubmed/34155268 http://dx.doi.org/10.1038/s41598-021-92435-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Yu, Jie-Mei Fu, Yuan-Hui Peng, Xiang-Lei Zheng, Yan-Peng He, Jin-Sheng Genetic diversity and molecular evolution of human respiratory syncytial virus A and B |
title | Genetic diversity and molecular evolution of human respiratory syncytial virus A and B |
title_full | Genetic diversity and molecular evolution of human respiratory syncytial virus A and B |
title_fullStr | Genetic diversity and molecular evolution of human respiratory syncytial virus A and B |
title_full_unstemmed | Genetic diversity and molecular evolution of human respiratory syncytial virus A and B |
title_short | Genetic diversity and molecular evolution of human respiratory syncytial virus A and B |
title_sort | genetic diversity and molecular evolution of human respiratory syncytial virus a and b |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8217232/ https://www.ncbi.nlm.nih.gov/pubmed/34155268 http://dx.doi.org/10.1038/s41598-021-92435-1 |
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