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Evolutionary genetics of genotype H1 measles viruses in China from 1993 to 2012
Virologic surveillance is a critical component of measles management. One of the criteria for verification of elimination of endemic measles is genetic analysis of wild-type viruses to demonstrate lack of an indigenous genotype. Measles is yet to be eliminated in China, and genotype H1 has been dete...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society for General Microbiology
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4135087/ https://www.ncbi.nlm.nih.gov/pubmed/24914068 http://dx.doi.org/10.1099/vir.0.066746-0 |
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author | Xu, Songtao Zhang, Yan Rivailler, Pierre Wang, Huiling Ji, Yixin Zhen, Zhu Mao, Naiying Li, Chongshan Bellini, William J. Xu, Wenbo Rota, Paul A. |
author_facet | Xu, Songtao Zhang, Yan Rivailler, Pierre Wang, Huiling Ji, Yixin Zhen, Zhu Mao, Naiying Li, Chongshan Bellini, William J. Xu, Wenbo Rota, Paul A. |
author_sort | Xu, Songtao |
collection | PubMed |
description | Virologic surveillance is a critical component of measles management. One of the criteria for verification of elimination of endemic measles is genetic analysis of wild-type viruses to demonstrate lack of an indigenous genotype. Measles is yet to be eliminated in China, and genotype H1 has been detected continuously since virologic surveillance was initiated in 1993. Virologic surveillance has been very active in China, providing a unique opportunity to conduct a detailed study of the evolution of a single, endemic genotype over a timespan of nearly two decades. Phylogenetic analysis performed on the 450 nt coding sequence for the C-terminal 150 amino acids of the nucleoprotein (N-450), fusion (F) gene and haemagglutinin (H) gene confirmed the continued circulation of genotype H1 viruses for 19 years. No evidence of selective pressure for the H protein was found. The substitution rates ranged from 0.75×10(−3) substitutions site(−1) year(−1) for H to 1.65×10(−3) substitutions site(−1) year(−1) for N-450. The time of most recent common ancestor (TMRCA) for genotype H1 was estimated as approximately 1985 (95 % highest probability density, 1979–1989). Finally, the overall diversity of measles sequences from China decreased from 2005 to 2012, coincident with a substantial decrease in measles cases. The results suggest that detailed evolutionary analyses should facilitate the documentation of eventual measles elimination in China. Moreover, the molecular approaches used in this study can be applied in other countries approaching measles elimination. |
format | Online Article Text |
id | pubmed-4135087 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Society for General Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-41350872014-09-01 Evolutionary genetics of genotype H1 measles viruses in China from 1993 to 2012 Xu, Songtao Zhang, Yan Rivailler, Pierre Wang, Huiling Ji, Yixin Zhen, Zhu Mao, Naiying Li, Chongshan Bellini, William J. Xu, Wenbo Rota, Paul A. J Gen Virol Animal Virologic surveillance is a critical component of measles management. One of the criteria for verification of elimination of endemic measles is genetic analysis of wild-type viruses to demonstrate lack of an indigenous genotype. Measles is yet to be eliminated in China, and genotype H1 has been detected continuously since virologic surveillance was initiated in 1993. Virologic surveillance has been very active in China, providing a unique opportunity to conduct a detailed study of the evolution of a single, endemic genotype over a timespan of nearly two decades. Phylogenetic analysis performed on the 450 nt coding sequence for the C-terminal 150 amino acids of the nucleoprotein (N-450), fusion (F) gene and haemagglutinin (H) gene confirmed the continued circulation of genotype H1 viruses for 19 years. No evidence of selective pressure for the H protein was found. The substitution rates ranged from 0.75×10(−3) substitutions site(−1) year(−1) for H to 1.65×10(−3) substitutions site(−1) year(−1) for N-450. The time of most recent common ancestor (TMRCA) for genotype H1 was estimated as approximately 1985 (95 % highest probability density, 1979–1989). Finally, the overall diversity of measles sequences from China decreased from 2005 to 2012, coincident with a substantial decrease in measles cases. The results suggest that detailed evolutionary analyses should facilitate the documentation of eventual measles elimination in China. Moreover, the molecular approaches used in this study can be applied in other countries approaching measles elimination. Society for General Microbiology 2014-09 /pmc/articles/PMC4135087/ /pubmed/24914068 http://dx.doi.org/10.1099/vir.0.066746-0 Text en http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Animal Xu, Songtao Zhang, Yan Rivailler, Pierre Wang, Huiling Ji, Yixin Zhen, Zhu Mao, Naiying Li, Chongshan Bellini, William J. Xu, Wenbo Rota, Paul A. Evolutionary genetics of genotype H1 measles viruses in China from 1993 to 2012 |
title | Evolutionary genetics of genotype H1 measles viruses in China from 1993 to 2012 |
title_full | Evolutionary genetics of genotype H1 measles viruses in China from 1993 to 2012 |
title_fullStr | Evolutionary genetics of genotype H1 measles viruses in China from 1993 to 2012 |
title_full_unstemmed | Evolutionary genetics of genotype H1 measles viruses in China from 1993 to 2012 |
title_short | Evolutionary genetics of genotype H1 measles viruses in China from 1993 to 2012 |
title_sort | evolutionary genetics of genotype h1 measles viruses in china from 1993 to 2012 |
topic | Animal |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4135087/ https://www.ncbi.nlm.nih.gov/pubmed/24914068 http://dx.doi.org/10.1099/vir.0.066746-0 |
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