文章摘要
屈勇刚,剡根强,杨国庆,邹洋,陈化新,张永振.辽宁省葫芦岛地区鼠类汉坦病毒的分离与鉴定[J].中华流行病学杂志,2006,27(6):513-517
辽宁省葫芦岛地区鼠类汉坦病毒的分离与鉴定
Isolation and characterization of Hantavirus carried by rodents in Huludao, Liaoning province
收稿日期:2005-09-15  出版日期:2014-09-12
DOI:
中文关键词: 汉坦病毒  病毒分离  逆转录-聚合酶链反应  系统发生分析
英文关键词: Hantavirus  Isolation of virus  Reverse transcriptase-polymerase chain reaction  Phylogenetic analysis
基金项目:科技部科研院所社会公益研究专项资金项目(2002DIB40095);国家“十五”科技攻关课题资助项目(2003BA712A08-02)
作者单位E-mail
屈勇刚 新疆石河子大学动物科技学院, 石河子 832003  
剡根强 新疆石河子大学动物科技学院, 石河子 832003  
杨国庆 辽宁省葫芦岛市疾病预防控制中心  
邹洋 中国疾病预防控制中心传染病预防控制所  
陈化新 中国疾病预防控制中心传染病预防控制所  
张永振 中国疾病预防控制中心传染病预防控制所 yongzhenzhang@sohu.com 
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中文摘要:
      目的研究葫芦岛地区鼠类中汉坦病毒的感染流行情况以及病毒的型别。方法采用夹夜法捕捉鼠类,间接免疫荧光法检测鼠肺中的汉坦病毒抗原,阳性较强的标本接种到Vero E6细胞分离病毒,RT-PCR对分离的病毒与阳性样品扩增核苷酸片段并测序,构建系统发生树进行分型与系统发生分析。结果在200份鼠肺标本中共检测到11个样品阳性,阳性率为5.5%。选择阳性较强的标本,接种到Vero E6细胞并连续传代后分离到3株病毒。用S片段(620-999 nt)与M片段G1区(180-580 nt)的核苷酸构建的系统发生树,结果表明葫芦岛分离的3株病毒均为S3亚型。用G2区的2003-2302 nt的核苷酸序列构建的系统发生树将来自不同地区的SEO型病毒可分为7个亚型,其中从葫芦岛地区分离的3株病毒与北京地区分离株CP211、ch302、dc501和山东省分离株SD10、SD227株的亲缘关系最近。结论葫芦岛地区鼠类中汉坦病毒的携带率较高,主要流行S3亚型SEOV。
英文摘要:
      Objective To investigate the Hantavirus infection and their genotype in rodents in Huludao.Methods Rodents were collected from the main epidemic areas to detect antigen of Hantavirus in rat lungs by indirect immunofluorescence assay. Antigen-positive samples were inoculated onto cultures of confluent Vero E6 cells for the isolation of virus. The genotypes of viruses in all antigen-positive samples were identified by reverse transcriptase-polymerase chain reaction (RT-PCR). Results 200 rats were collected in the main epidemic areas, and 11 Hantavirus-positive samples were tested. The positive rate of Hantavirus in rats was 5.5%. Three strains of Hantavirus were isolated in Vero E6 cell culture. Data from the phylogenetic trees constructed by partial S segment (620-999 nt) or partial Gl segment (180-580 nt) showed that the three isolates carried by rats from Huludao were all genetic subtype SEOV 3. Furthermore, the phylogenetic tree constructed by partial G2 segment (2003- 2302 nt) divided SEOV strains into 7 genetic subtypes, and the three isolates were having a closer evolutionary relationship with isolates CP211, ch302 and dc501 from Beijing, and the isolates SD10 and SD227 form Shandong. Conclusion Data indicated that the rate of carrying virus was high and the main genetic subtype of Hantavirus was S3 of Seoul virus in Huludao area.
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