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乌鸡传染性法氏囊病毒VP2基因的克隆与序列分析
引用本文:张春杰,程相朝,李银聚. 乌鸡传染性法氏囊病毒VP2基因的克隆与序列分析[J]. 西北农林科技大学学报(自然科学版), 2004, 32(3): 33-36
作者姓名:张春杰  程相朝  李银聚
作者单位:河南科技大学,动物科技学院,河南,洛阳,471003
基金项目:河南省骨干教师资助项目(2003056)
摘    要:应用RT-PCR法,对分离于当地典型发病乌鸡群的IBDV(WJ株)进行了VP2基因的克隆与序列分析,并和相关毒株进行了比较。结果表明,WJ株与标准血清 型STC株的核苷酸和氨基酸的同源性只有91.39%和92.74%,而与超强毒株UK661和从当地鸡群中分离的超强毒株HN01株的核苷酸和氨基酸的同源性则较高,其中,与其核苷酸同源性分别为95.43%和95.87%,与其氨基酸同源性均为96.77%。且该毒株的VP2基因序列完全具备超强毒株的主要特征。由此说明,分离于当地发病乌鸡群的IBDV为超强毒株,并和当地流行的鸡IBD超强毒株有较高的同源性,但也有明显的差异。

关 键 词:乌鸡  IBDV  VP2基因  克隆  序列分析
文章编号:1671-9387(2004)03-0033-04
收稿时间:2003-07-22
修稿时间:2003-07-22

Cloning and sequence analysis of the VP2 gene of IBDV isolated from dark-bone chicken
ZHANG Chun-jie,CHENG Xiang-chao,LI Yin-ju,WU Ting-cai,WANG Shu-fang. Cloning and sequence analysis of the VP2 gene of IBDV isolated from dark-bone chicken[J]. Journal of Northwest A&F University(Natural Science Edition), 2004, 32(3): 33-36
Authors:ZHANG Chun-jie  CHENG Xiang-chao  LI Yin-ju  WU Ting-cai  WANG Shu-fang
Affiliation:(College of Animal Science and Technology,Henan University of Science and Technology,Luoyang,Henan 471003,China)
Abstract:The VP2 gene of IBDV (WJ strain) isolated from dark-bone chicken were amplified by RT-PCR and cloned into pMD18-T vector to analysed sequence.Sequence comparison with standard I sterotype IBDV (STC),the homology of the nucleotide and amino acid were only 91.39% and 92.74%,separately;But comparison with very-virulent IBDV (vv IBDV) UK661 and HN01,the homology of nucleotide were 95.43% and 95.87%,96.77%;the homology of amino acid all were 96.77%.Moreover,the VP2 gene sequence of WJ strain possessed completely the characteristics of vv IBDV.The results showed that WJ strain was a very-virulent IBDV.
Keywords:dark-bone chicken  IBDV  VP2 gene  cloning  sequence analysis
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