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免疫抗体压力下PRRSVGD株Nsp2和GP5基因变异分析
引用本文:牛晓芸,李康宁,贺东生.免疫抗体压力下PRRSVGD株Nsp2和GP5基因变异分析[J].广东畜牧兽医科技,2012,37(6):29-31,37.
作者姓名:牛晓芸  李康宁  贺东生
作者单位:1. 华南农业大学兽医学院,广东广州,510642
2. 中牧实业股份有限公司,北京,100070
3. 华南农业大学兽医学院,广东广州510642 广东省兽用生物制品技术研究与应用企业重点实验室,广东广州510640
摘    要:以PRRSVGD-2007株为材料,在自然条件和抗体压力下连续传至40代后,分别命名为PRRSV—GD—f40和PRRSV—GDAb—f40,进行RT—PCR,扩增Nsp2基因部分序列和GP5基因全长,克隆并测序。应用序列分析软件将测序结果和已经发表的PRRSV毒株进行比对,结果显示:Nsp2基因扩增片段大小均为796bp,自然传代和抗体压力下传代后的新毒株和母源毒株的相似性分别为98.0%和97.9%;扩增的GP5基因大小为603bp,编码200个氨基酸,和母源毒株的相似性分别为99.2%和98.8%。

关 键 词:猪繁殖与呼吸综合征病毒  Nsp2  GP5  序列分析

Variation Analysis of the Nsp2 and GP5 Gene ofPRRSV (GD strain) under Antibody Selective Pressures
Niu Xiaoyun,Li Kangning,He Dongsheng.Variation Analysis of the Nsp2 and GP5 Gene ofPRRSV (GD strain) under Antibody Selective Pressures[J].Guangdong Journal of Animal and Veterinary Science,2012,37(6):29-31,37.
Authors:Niu Xiaoyun  Li Kangning  He Dongsheng
Institution:1,2(1.College of Veterinary Medicine,South China Agricultural University,Guangzhou 510642,China;2.Guangdong Veterinary Biological Products Technology Research and Application Enterprise key Laboratories,Guangzhou 510640,China;3.China Animal Husbandry Industry CO.,Ltd,Beijing,100070,China)
Abstract:PRRSV strain GD was continuously propagated in Marc-145 cells for 40 passages without PRRSV antibody or with PRRSV antibody and the viruses after passages were named RRRSV-GD-f40 or RRRSV-GDAb-f40 respectively. Nsp2 and GP5 genes were cloned and sequenced. Comparison results showed that the amplification fragment of Nsp2 gene of all isolates were 796 bp long and shared 98.0% or 97.9% similirities with maternal strain respectively. The GP5 genome analyses showed that their cDNAs of GP5 were 603bp long and shared 99.2% or 98.8% similirities with maternal strain respectively.
Keywords:PRRSV  Nsp2  GP5  Sequence analysis
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