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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
张春杰1, 程相朝1, 李银聚1
河南科技大学 动物科技学院
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Ⅰ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
DOI:
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基金项目:河南省骨干教师资助项目(2003056)
Cloning and sequence analysis of the VP2 gene of IBDV isolated from dark-bone chicken
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.
Key words:  dark-bone chicken  IBDV  VP2 gene  cloning  sequence analysis

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