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鹅副粘病毒GX1株的HN和F蛋白基因的克隆和序列分析
引用本文:易春华,潘杰,付薇,颜健华,徐贤坤,熊毅.鹅副粘病毒GX1株的HN和F蛋白基因的克隆和序列分析[J].农业科学与技术,2009,10(4):75-78.
作者姓名:易春华  潘杰  付薇  颜健华  徐贤坤  熊毅
作者单位:易春华,潘杰(广西大学动物科学技术学院,广西南宁,530005);付薇,颜健华,徐贤坤,熊毅(广西壮族自治区动物疫病预防控制中心,广西南宁,530001) 
基金项目:the Development Program for Guangxi Science and Technology(0719004-3G).广西科技攻关项目 
摘    要:1材料与方法 1.1病毒来源鹅副粘病毒分离株GX1株由广西壮族自治区动物疫病预防控制中心实验室分离保存。 1.2试剂及仪器各种PCR反应试剂、PMD-18T载体、胶回收试剂盒、限制性内切酶等均购自宝生物工程(大连)公司。仪器:恒温孵化箱、PCR反应仪、超速离心机、移液器等。

关 键 词:鹅副粘病毒  F蛋白基因  序列分析  广西壮族自治区  病毒分离株  PCR反应  克隆  动物疫病预防

Cloning and Sequence Analysis of HN and F Protein Genes from a Strain of Goose Paramyxovirus
YI Chun-hua,PAN Jie,FU Wei,YAN Jian-hua,XU Xian-kun,XIONG Yi.Cloning and Sequence Analysis of HN and F Protein Genes from a Strain of Goose Paramyxovirus[J].Agricultural Science & Technology,2009,10(4):75-78.
Authors:YI Chun-hua  PAN Jie  FU Wei  YAN Jian-hua  XU Xian-kun  XIONG Yi
Institution:1. College of Animal Science and Technology, Guangxi University, Nanning 530005; 2. Guangxi Provincial Center for Animal Disease Control and Prevention, Nanning 530001)
Abstract: Objective] The study was to clone HN and F genes from GX1 strain of goose paramyxovirus and analyze their sequences. Method] According to the full nucleotide sequence of GPV-SF02 strain of goose paramyxovirus, two pairs of pdmers were designed to amplify the HN and F genes from GX1 strain of goose paramyxovirus isolated from diseased goose in Guangxi Zhuang Autonomous Region; the amplified products were ligated into pMD18-T vector and sequenced. Result ] HN and F genes of this strain tested were 1 716 and 1 662 bp in full nucleotide length, respectively; both showed the homologues of about 97.3% with GPV- SF02 strain, of 80.3% -97.5% with strains LaSota, F48E9 and JS, of just 84.8% with Miyadera strain. Conclusion] The results show that isolated strain BX1 matches to virulent APMV-1 strain, belonging to genotype Ⅶ of APMV-1 strain.
Keywords:Goose paramyxovirus  HN protein gene  F protein gene  Cloning  Sequence analysis
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