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Molecular characterization of structural protein genes of dengue virus serotype 1 epidemic in Yunnan, Southwest China, in 2018

A dengue virus serotype 1 (DENV-1) epidemic occurred from October to December 2018 in Xishuangbanna, Yunnan, Southwest China, neighboring Myanmar, Laos, and Vietnam. In this study, we investigated the molecular characteristics, evolution, and potential source of DENV from Xishuangbanna. The C (capsi...

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Autores principales: Lan, Qingping, Shu, Yun, Li, Linhao, Shan, Xiyun, Ma, Dehong, Li, Tingting, Wang, Xiaodan, Pan, Yue, Chen, Junying, Zhang, Juan, Liu, Pinghua, Sun, Qiangming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Vienna 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7831630/
https://www.ncbi.nlm.nih.gov/pubmed/33495898
http://dx.doi.org/10.1007/s00705-020-04942-7
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author Lan, Qingping
Shu, Yun
Li, Linhao
Shan, Xiyun
Ma, Dehong
Li, Tingting
Wang, Xiaodan
Pan, Yue
Chen, Junying
Zhang, Juan
Liu, Pinghua
Sun, Qiangming
author_facet Lan, Qingping
Shu, Yun
Li, Linhao
Shan, Xiyun
Ma, Dehong
Li, Tingting
Wang, Xiaodan
Pan, Yue
Chen, Junying
Zhang, Juan
Liu, Pinghua
Sun, Qiangming
author_sort Lan, Qingping
collection PubMed
description A dengue virus serotype 1 (DENV-1) epidemic occurred from October to December 2018 in Xishuangbanna, Yunnan, Southwest China, neighboring Myanmar, Laos, and Vietnam. In this study, we investigated the molecular characteristics, evolution, and potential source of DENV from Xishuangbanna. The C (capsid), prM (premembrane), and E (envelope) genes of DENV isolated from 87 serum samples obtained from local patients were amplified and sequenced, and the sequences were evaluated by identification of mutations, phylogenetic and homologous recombination analysis, and secondary structure prediction. Phylogenetic analysis showed that all of the epidemic DENV strains from Xishuangbanna could be grouped in a branch with DENV-1 isolates, and were most similar to the Fujian 2005 (China, DQ193572) and Singapore 2016 (MF314188) strains. When compared with DENV-1SS (the standard strain), there were 31 non-synonymous mutations, but no obvious homologous recombination signal was found. Secondary structure prediction showed that some changes had occurred in a helical region in proteins of the MN123849 and MN123854 strains, but there were few changes in the disordered region. This study reveals the molecular characteristics of the structural genes of the Xishuangbanna epidemic strains in 2018 and provides a reference for molecular epidemiology, infection, and pathogenicity research and vaccine development.
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spelling pubmed-78316302021-01-26 Molecular characterization of structural protein genes of dengue virus serotype 1 epidemic in Yunnan, Southwest China, in 2018 Lan, Qingping Shu, Yun Li, Linhao Shan, Xiyun Ma, Dehong Li, Tingting Wang, Xiaodan Pan, Yue Chen, Junying Zhang, Juan Liu, Pinghua Sun, Qiangming Arch Virol Original Article A dengue virus serotype 1 (DENV-1) epidemic occurred from October to December 2018 in Xishuangbanna, Yunnan, Southwest China, neighboring Myanmar, Laos, and Vietnam. In this study, we investigated the molecular characteristics, evolution, and potential source of DENV from Xishuangbanna. The C (capsid), prM (premembrane), and E (envelope) genes of DENV isolated from 87 serum samples obtained from local patients were amplified and sequenced, and the sequences were evaluated by identification of mutations, phylogenetic and homologous recombination analysis, and secondary structure prediction. Phylogenetic analysis showed that all of the epidemic DENV strains from Xishuangbanna could be grouped in a branch with DENV-1 isolates, and were most similar to the Fujian 2005 (China, DQ193572) and Singapore 2016 (MF314188) strains. When compared with DENV-1SS (the standard strain), there were 31 non-synonymous mutations, but no obvious homologous recombination signal was found. Secondary structure prediction showed that some changes had occurred in a helical region in proteins of the MN123849 and MN123854 strains, but there were few changes in the disordered region. This study reveals the molecular characteristics of the structural genes of the Xishuangbanna epidemic strains in 2018 and provides a reference for molecular epidemiology, infection, and pathogenicity research and vaccine development. Springer Vienna 2021-01-25 2021 /pmc/articles/PMC7831630/ /pubmed/33495898 http://dx.doi.org/10.1007/s00705-020-04942-7 Text en © The Author(s), under exclusive licence to Springer-Verlag GmbH, AT part of Springer Nature 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Original Article
Lan, Qingping
Shu, Yun
Li, Linhao
Shan, Xiyun
Ma, Dehong
Li, Tingting
Wang, Xiaodan
Pan, Yue
Chen, Junying
Zhang, Juan
Liu, Pinghua
Sun, Qiangming
Molecular characterization of structural protein genes of dengue virus serotype 1 epidemic in Yunnan, Southwest China, in 2018
title Molecular characterization of structural protein genes of dengue virus serotype 1 epidemic in Yunnan, Southwest China, in 2018
title_full Molecular characterization of structural protein genes of dengue virus serotype 1 epidemic in Yunnan, Southwest China, in 2018
title_fullStr Molecular characterization of structural protein genes of dengue virus serotype 1 epidemic in Yunnan, Southwest China, in 2018
title_full_unstemmed Molecular characterization of structural protein genes of dengue virus serotype 1 epidemic in Yunnan, Southwest China, in 2018
title_short Molecular characterization of structural protein genes of dengue virus serotype 1 epidemic in Yunnan, Southwest China, in 2018
title_sort molecular characterization of structural protein genes of dengue virus serotype 1 epidemic in yunnan, southwest china, in 2018
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7831630/
https://www.ncbi.nlm.nih.gov/pubmed/33495898
http://dx.doi.org/10.1007/s00705-020-04942-7
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