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鸡传染性法氏囊病病毒XX08株VP2高变区基因的克隆与序列分析 被引量:3

Cloning and Analysis of Highly Variable Region VP2 Gene in Infectious bursal disease virus XX08 Strain
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摘要 应用反转录(RT-PCR)技术从河南新乡某鸡场分离的鸡传染性法氏囊病病毒XX08株总RNA中克隆出593bp的VP2高变区基因。序列分析表明,XX08毒株VP2高变区氨基酸序列与欧洲超强毒株UK661、日本超强毒株OKYM以及经典弱毒株D78的同源性均为96.8%。遗传进化分析表明,该毒株与超强毒株UK661和OKYM位于同一进化树。XX08毒株与超强毒株具有相似的氨基酸特征,但是222位的A被P替代,提示XX08毒株可能为中等强毒力毒株。 The Infectious bursal disease virus(IBDV)XX08 strain was isolated from a chicken farm in Xinxiang city of Henan province.The highly variable region VP2 gene,593 bp,was cloned from the total RNA of the XX08 strain by RT-PCR.Amino acid sequence analysis showed that there was 96.8% homology among the European vvIBDV strain of OKYM,Japanese UK661,classical attenuated strain D78 and the isolated strain of XX08.Compared with the highly variable region of these strain,the amino acid residue A in 222 position of polyprotein of IBDV was substituted with P.The phylogenetic analysis showed that the XX08 strain was in the same lineage with the European and Japanese vvIBDV.These data suggested that the XX08 strain was probably the moderate virulent IBDV.
出处 《动物医学进展》 CSCD 北大核心 2010年第3期35-39,共5页 Progress In Veterinary Medicine
基金 国家自然科学基金项目(30871885)
关键词 传染性法氏囊病病毒 VP2 克隆 Infectious bursal disease virus VP2 cloning
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