《中国畜牧兽医》 ›› 2018, Vol. 45 ›› Issue (8): 2057-2066.doi: 10.16431/j.cnki.1671-7236.2018.08.003

• 生物技术 • 上一篇    下一篇

基于N基因的小反刍兽疫病毒贵州流行株分子特征与分群研究

王军1,2, 杨源1,2, 张云丹1,2, 文明1,2, 周碧君1,2, 程振涛1,2, 岳筠3, 李涛3   

  1. 1. 贵州大学动物科学学院, 贵阳 550025;
    2. 贵州省动物疫病与兽医公共卫生重点实验室, 贵阳 550025;
    3. 贵州省动物疫病预防控制中心, 贵阳 550008
  • 收稿日期:2018-01-17 出版日期:2018-08-20 发布日期:2018-08-15
  • 通讯作者: 程振涛, 李涛 E-mail:chengzhentao@sohu.com;727670509@qq.com
  • 作者简介:王军(1993-),男,贵州麻江人,硕士生,研究方向:动物疫病病原学,E-mail:871163492@qq.com
  • 基金资助:

    贵州省科技合作项目(黔科合LH字(2015)7674号);贵州省研究生教育创新计划项目(GZZ2017002);贵州省科技创新人才团队项目(黔科合人才团队(2015)4016号)

Molecular Characteristics and Cluster of PPRV Guizhou Strains Based on N Gene

WANG Jun1,2, YANG Yuan1,2, ZHANG Yundan1,2, WEN Ming1,2, ZHOU Bijun1,2, CHENG Zhentao1,2, YUN Jun3, LI Tao3   

  1. 1. College of Animal Science, Guizhou University, Guiyang 550025, China;
    2. Key Laboratory of Animal Health and Veterinary Public Health, Guizhou Province, Guiyang 550025, China;
    3. Guizhou Animal Disease Prevention and Control Center, Guiyang 550008, China
  • Received:2018-01-17 Online:2018-08-20 Published:2018-08-15

摘要:

为探讨小反刍兽疫病毒(peste des petits ruminants virus,PPRV)贵州流行株N基因分子特征和分群,试验设计了1对特异性引物,应用RT-PCR技术对小反刍兽疫(peste des petits ruminants,PPR)临床样本进行N基因扩增,克隆至pMD19-T载体,对阳性重组质粒进行测序,应用DANStar软件对测序序列和参考序列进行核苷酸同源性、氨基酸同源性、变异位点及系统进化树分析。结果显示:PPRV贵州流行株N基因扩增长度为1 578 bp,其相互间核苷酸、氨基酸同源性分别为99.6%~100.0%及99.2%~100.0%,与国内参考株N基因的核苷酸序列(97.7%~99.9%)及氨基酸序列(98.3%~100.0%)同源性较国外参考株(88.5%~97.7%和92.2%~98.5%)高;PPRV贵州流行株N基因编码的氨基酸同疫苗株Nigeria 75-1相比存在26个位点突变,但没有氨基酸的缺失或增加;基于N基因系统进化分析显示,PPRV贵州流行株同国内参考株处于同一个进化分支,但与国外参考株处于不同进化分支;其属于病毒进化的Ⅳ基因群,与国内参考株处于同一系统分群,但与疫苗株Nigeria 75-1(Ⅰ基因群)处于不同基因群。

关键词: 小反刍兽疫病毒(PPRV); N基因; 序列分析; 基因分群

Abstract:

In order to investigate the N gene molecular characteristics and clustering of the peste des petits ruminants virus (PPRV) of Guizhou province,the primers of PPRV N gene were designed and the target gene was amplified from clinical samples and then was cloned to pMD19-T vector.The positive recombinant plasmids were sequenced and nucleotide homologoy, amino acids homology,mutation sites and phylogenetic tree analysis of N gene of Guizhou PPRV strains and reference strains were performed by DANStar software.The results showed that the length of amplified N gene was 1 578 bp and the homology of nucleotide and amino acid sequences among Guizhou PPRV strains were 99.6% to 100.0% and 99.2% to 100.0%,respectively.The homology of nucleotide (97.7% to 99.9%) and amino acids (98.3% to 100.0%) compared with domestic reference strains were higher than those of other countries (88.5% to 97.7% and 92.2% to 98.5%).Compared with the vaccine strain Nigeria 75-1,there were 26 multiple sites in N gene of Guizhou PPRV strains while there was no amino acid loss or increase.The results of phylogenetic analysis showed that Guizhou PPRV strains were in the same evolutionary branch with the domestic reference strains,while the foreign reference strains in a different evolutionary branch.Guizhou PPRV strains belonged to Ⅳ gene group and vaccine strain Nigeria 75-1 belonged to Ⅰ gene group.

Key words: peste des petits ruminants virus (PPRV); N gene; sequence analysis; gene grouping

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