Cargando…

Gradual replacement of all previously circulating respiratory syncytial virus A strain with the novel ON1 genotype in Lanzhou from 2010 to 2017

ON1 is a novel genotype of human respiratory syncytial virus (HRSV) subtype A, in children with acute respiratory tract infections (ARTIs). However, there is not much data on the prevalence and clinical and molecular characterization in China. Our study is based on the children who had respiratory i...

Descripción completa

Detalles Bibliográficos
Autores principales: Liang, Xuan, Liu, Dong-Hai, Chen, De, Guo, Li, Yang, Hui, Shi, Yong-Sheng, Wang, Yong-Jun, Wang, Wei-Kai, Xie, Zhi-Ping, Gao, Han-Chun, Duan, Zhao-Jun, Zhang, Rong-Fang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6531141/
https://www.ncbi.nlm.nih.gov/pubmed/31083208
http://dx.doi.org/10.1097/MD.0000000000015542
_version_ 1783420766822334464
author Liang, Xuan
Liu, Dong-Hai
Chen, De
Guo, Li
Yang, Hui
Shi, Yong-Sheng
Wang, Yong-Jun
Wang, Wei-Kai
Xie, Zhi-Ping
Gao, Han-Chun
Duan, Zhao-Jun
Zhang, Rong-Fang
author_facet Liang, Xuan
Liu, Dong-Hai
Chen, De
Guo, Li
Yang, Hui
Shi, Yong-Sheng
Wang, Yong-Jun
Wang, Wei-Kai
Xie, Zhi-Ping
Gao, Han-Chun
Duan, Zhao-Jun
Zhang, Rong-Fang
author_sort Liang, Xuan
collection PubMed
description ON1 is a novel genotype of human respiratory syncytial virus (HRSV) subtype A, in children with acute respiratory tract infections (ARTIs). However, there is not much data on the prevalence and clinical and molecular characterization in China. Our study is based on the children who had respiratory infections positive for RSV-A admitted by Gansu Provincial Maternity and Child-care Hospital in Lanzhou (northwestern China) during the last 7 epidemic seasons from 2010 to 2017. In our study, different strains of the novel RSV-A genotype ON1, first identified in Canada in December 2010, were first detected in Gansu Provincial Maternity and Child-care Hospital in August 2012 and then followed by an abrupt expansion in the number of ON1 variants in the beginning of 2014 and eventually replaced all other RSV-A strains from 2015 to 2017. ON1 is characterized by a 72-nt duplication in the C-terminal region of the highly variable attachment glycoprotein (G), predicted to lengthen the polypeptide with 24 amino acids, including a 23-aa duplication, which likely changes antigenicity. New N-glycosylation sites occurred within the 23-aa duplication and 24-aa insertion of the ON1 viruses in our study. Notably, RSV infections occurred later, but peaked sooner from the 2014/2015 to 2016/2017 epidemic seasons, compared with the previous 4 seasons. Our study concluded that genotype ON1 has caused larger outbreaks and became the predominate genotype for HRSV subgroup A in Lanzhou from 2013 to 2017, and became the sole genotype of RSV-A in 2015/2016 and 2016/2017. Our data indicate that northwest of China and the world will eventually be dominated by the ON1 RSV-A genotype, including the possibility for vaccine development. Based on trends seen in RSV-B BA genotype, which predominated for decades, there is a possibility to develop a vaccine for children in the next 10 years.
format Online
Article
Text
id pubmed-6531141
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Wolters Kluwer Health
record_format MEDLINE/PubMed
spelling pubmed-65311412019-06-25 Gradual replacement of all previously circulating respiratory syncytial virus A strain with the novel ON1 genotype in Lanzhou from 2010 to 2017 Liang, Xuan Liu, Dong-Hai Chen, De Guo, Li Yang, Hui Shi, Yong-Sheng Wang, Yong-Jun Wang, Wei-Kai Xie, Zhi-Ping Gao, Han-Chun Duan, Zhao-Jun Zhang, Rong-Fang Medicine (Baltimore) Research Article ON1 is a novel genotype of human respiratory syncytial virus (HRSV) subtype A, in children with acute respiratory tract infections (ARTIs). However, there is not much data on the prevalence and clinical and molecular characterization in China. Our study is based on the children who had respiratory infections positive for RSV-A admitted by Gansu Provincial Maternity and Child-care Hospital in Lanzhou (northwestern China) during the last 7 epidemic seasons from 2010 to 2017. In our study, different strains of the novel RSV-A genotype ON1, first identified in Canada in December 2010, were first detected in Gansu Provincial Maternity and Child-care Hospital in August 2012 and then followed by an abrupt expansion in the number of ON1 variants in the beginning of 2014 and eventually replaced all other RSV-A strains from 2015 to 2017. ON1 is characterized by a 72-nt duplication in the C-terminal region of the highly variable attachment glycoprotein (G), predicted to lengthen the polypeptide with 24 amino acids, including a 23-aa duplication, which likely changes antigenicity. New N-glycosylation sites occurred within the 23-aa duplication and 24-aa insertion of the ON1 viruses in our study. Notably, RSV infections occurred later, but peaked sooner from the 2014/2015 to 2016/2017 epidemic seasons, compared with the previous 4 seasons. Our study concluded that genotype ON1 has caused larger outbreaks and became the predominate genotype for HRSV subgroup A in Lanzhou from 2013 to 2017, and became the sole genotype of RSV-A in 2015/2016 and 2016/2017. Our data indicate that northwest of China and the world will eventually be dominated by the ON1 RSV-A genotype, including the possibility for vaccine development. Based on trends seen in RSV-B BA genotype, which predominated for decades, there is a possibility to develop a vaccine for children in the next 10 years. Wolters Kluwer Health 2019-05-13 /pmc/articles/PMC6531141/ /pubmed/31083208 http://dx.doi.org/10.1097/MD.0000000000015542 Text en Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle Research Article
Liang, Xuan
Liu, Dong-Hai
Chen, De
Guo, Li
Yang, Hui
Shi, Yong-Sheng
Wang, Yong-Jun
Wang, Wei-Kai
Xie, Zhi-Ping
Gao, Han-Chun
Duan, Zhao-Jun
Zhang, Rong-Fang
Gradual replacement of all previously circulating respiratory syncytial virus A strain with the novel ON1 genotype in Lanzhou from 2010 to 2017
title Gradual replacement of all previously circulating respiratory syncytial virus A strain with the novel ON1 genotype in Lanzhou from 2010 to 2017
title_full Gradual replacement of all previously circulating respiratory syncytial virus A strain with the novel ON1 genotype in Lanzhou from 2010 to 2017
title_fullStr Gradual replacement of all previously circulating respiratory syncytial virus A strain with the novel ON1 genotype in Lanzhou from 2010 to 2017
title_full_unstemmed Gradual replacement of all previously circulating respiratory syncytial virus A strain with the novel ON1 genotype in Lanzhou from 2010 to 2017
title_short Gradual replacement of all previously circulating respiratory syncytial virus A strain with the novel ON1 genotype in Lanzhou from 2010 to 2017
title_sort gradual replacement of all previously circulating respiratory syncytial virus a strain with the novel on1 genotype in lanzhou from 2010 to 2017
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6531141/
https://www.ncbi.nlm.nih.gov/pubmed/31083208
http://dx.doi.org/10.1097/MD.0000000000015542
work_keys_str_mv AT liangxuan gradualreplacementofallpreviouslycirculatingrespiratorysyncytialvirusastrainwiththenovelon1genotypeinlanzhoufrom2010to2017
AT liudonghai gradualreplacementofallpreviouslycirculatingrespiratorysyncytialvirusastrainwiththenovelon1genotypeinlanzhoufrom2010to2017
AT chende gradualreplacementofallpreviouslycirculatingrespiratorysyncytialvirusastrainwiththenovelon1genotypeinlanzhoufrom2010to2017
AT guoli gradualreplacementofallpreviouslycirculatingrespiratorysyncytialvirusastrainwiththenovelon1genotypeinlanzhoufrom2010to2017
AT yanghui gradualreplacementofallpreviouslycirculatingrespiratorysyncytialvirusastrainwiththenovelon1genotypeinlanzhoufrom2010to2017
AT shiyongsheng gradualreplacementofallpreviouslycirculatingrespiratorysyncytialvirusastrainwiththenovelon1genotypeinlanzhoufrom2010to2017
AT wangyongjun gradualreplacementofallpreviouslycirculatingrespiratorysyncytialvirusastrainwiththenovelon1genotypeinlanzhoufrom2010to2017
AT wangweikai gradualreplacementofallpreviouslycirculatingrespiratorysyncytialvirusastrainwiththenovelon1genotypeinlanzhoufrom2010to2017
AT xiezhiping gradualreplacementofallpreviouslycirculatingrespiratorysyncytialvirusastrainwiththenovelon1genotypeinlanzhoufrom2010to2017
AT gaohanchun gradualreplacementofallpreviouslycirculatingrespiratorysyncytialvirusastrainwiththenovelon1genotypeinlanzhoufrom2010to2017
AT duanzhaojun gradualreplacementofallpreviouslycirculatingrespiratorysyncytialvirusastrainwiththenovelon1genotypeinlanzhoufrom2010to2017
AT zhangrongfang gradualreplacementofallpreviouslycirculatingrespiratorysyncytialvirusastrainwiththenovelon1genotypeinlanzhoufrom2010to2017