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免疫鸡群新城疫病毒的分离与分子鉴定 被引量:3

Isolation and Molecular Identification of Newcasttle Disease Virus from Immunized Chicken Flocks
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摘要 从免疫鸡群中分离到9株新城疫病毒(NDV),其中5株为强毒株,4株为中强毒株。用RT—PCR扩增F基因cDNA片段,并将其分别克隆到pGEM—Teasy载体中。序列分析结果表明,上述分离株F基因长度为1662bp,编码553个氨基酸,其F蛋白的氨基酸序列同源性为96.0%~99.8%;但与常见疫苗株的氨基酸同源性仅为87.6%~92.2%,F蛋白裂解位点序列为^112R-R-Q/R—K—R—FI—G^119,均属于基因Ⅶ型NDV。 Nine strains of Newcasttle disease virus(NDV) were isolated from immunized chicken flocks, 5 isolates of which were velogenic and the others were mesogenic. The cDNA fragments of F gene of 9 NDV strains above were amplified by RTPCR. The amplified fragments were cloned into pGEM-Teasy vector and the recombinant plasmids were sequenced. The results showed that the F gene from all of the NDV isolates consisted of 1 662 bp ,coding for 553 amino acids. The amino acid sequence homology among the 9 NDV isolates came to 96.0%-99.8% ,but the amino acid sequence homology between the 9 isolates and other NDV vaccine strains(LaSota,B1,F48E9 and Roakin) were relatively lower,from 87.6% to 92.2%. The sequence of cleavege site of F protein were ^112R-R-Q/R-K-R-F-I-G^119,all of the 9 isolates belonged to the genetype Ⅶ.
出处 《中国兽医学报》 CAS CSCD 北大核心 2006年第6期597-599,共3页 Chinese Journal of Veterinary Science
关键词 新城疫病毒(NDV) 分子鉴定 RT—PCR Newcasttle disease virus (NDV) molecular identification RT-PCR
作者简介 刘铀(1966-),男,副教授,博士。
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