中国媒介生物学及控制杂志 ›› 2020, Vol. 31 ›› Issue (5): 521-525.DOI: 10.11853/j.issn.1003.8280.2020.05.004

• 论著 • 上一篇    下一篇

浙江省衢州市2019年本地登革热暴发疫情的分子流行病学研究

杨瑞军, 黄世腾, 吕磊, 曹国平, 游佳玲, 万圣   

  1. 衢州市疾病预防控制中心微生物检验科/传染病防治科, 浙江 衢州 324000
  • 收稿日期:2020-04-10 出版日期:2020-10-20 发布日期:2020-10-20
  • 作者简介:杨瑞军,男,副主任技师,主要从事病原微生物学研究工作,Email:qzyangruijun@126.com
  • 基金资助:
    2019年衢州市科技计划指导性项目(2019127)

Molecular epidemiological study of local dengue outbreak in Quzhou, Zhejiang province, China, 2019

YANG Rui-jun, HUANG Shi-teng, LYU Lei, CAO Guo-ping, YOU Jia-ling, WAN Sheng   

  1. Quzhou City Center for Disease Control and Prevention, Quzhou 324000, Zhejiang Province, China
  • Received:2020-04-10 Online:2020-10-20 Published:2020-10-20
  • Supported by:
    Supported by the Scientific and Technological Guidance Project of Quzhou City (No.2019127)

摘要: 目的 对2019年衢州市本地登革热暴发疫情中检出的登革病毒1型进行序列测定和分子特征分析。方法 采集患者血清标本,采用胶体金免疫层析法和实时荧光定量PCR(RT-qPCR)方法分别检测登革病毒NS1抗原和病毒核酸;采用RT-qPCR方法扩增登革病毒E基因后进行序列测定,并与不同国家和地区的登革病毒株进行同源性和进化树分析。结果 从患者血清标本中检测到登革病毒NS1抗原和病毒核酸,经基因序列比对及进化分析,8株登革病毒均为登革1型的基因Ⅰ型,与JF960228(2010年新加坡分离株)互为姐妹群,且毒力位点1处发生变异。结论 从病原学、血清学和分子生物学证实该起暴发疫情是由登革1型病毒引起,该毒株有可能来源于东南亚,应加强中国与该地区登革热跨境传播的防控。

关键词: 本地病例, 登革热, 登革病毒, E基因, 序列分析, 生物信息学

Abstract: Objective To determine the nucleic acid sequence of the dengue type 1 virus (DENV-1) detected in the local dengue outbreak in Quzhou, Zhejiang province, China, 2019, and to analyze its molecular characteristics. Methods Serum samples were collected from dengue patients; colloidal gold immunochromatographic assay and quantitative real-time PCR (RT-qPCR) were used to detect the NS1 antigen and nucleic acid of dengue virus, respectively. The RT-qPCR assay was used to amplify the envelope gene of dengue virus, which was then sequenced. The genotype of the isolated strains was analyzed, and the homology and phylogenetic analyses were performed with the dengue strains isolated from other countries and regions. Results The serum samples of patients were positive for the NS1 antigen and nucleic acid of dengue virus. The gene sequence alignment and phylogenetic analysis showed that 8 dengue virus strains all belonged to DENV-1 subgenotype GI, which had the closest phylogenetic relationship with the strain JF960228 (Singapore, 2010), with a mutation at virulence locus 1. Conclusion It was confirmed by etiology, serology, and molecular biology that the local dengue outbreak was caused by DENV-1, which may originate from Southeast Asia. It is necessary to strengthen the prevention and control of cross-border spread of dengue fever in China and this region.

Key words: Local case, Dengue fever, Dengue virus, Envelope gene, Sequence analysis, Bioinformatics

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