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鸭新城疫病毒分离株抗原表位和遗传演化分析
引用本文:胡北侠,黄艳艳,路希山,张秀美,许传田,颜世敢,张伟.鸭新城疫病毒分离株抗原表位和遗传演化分析[J].中国兽医学报,2010,30(2).
作者姓名:胡北侠  黄艳艳  路希山  张秀美  许传田  颜世敢  张伟
作者单位:1. 山东省农业科学院,畜牧兽医研究所山东省畜禽疫病防治与繁育重点实验室,山东,济南,250100
2. 青岛农业大学,动物科技学院,山东,青岛,266109
基金项目:国家科技支撑计划,山东省科技攻关项目,农业科技成果转化基金
摘    要:从规模化养殖场鸭群气管和泄殖腔试子分离到新城疫病毒(NDV)27株,用2株针对NDV HN单抗进行抗原表位分析,并选择4个分离株进行F基因高变区(374bp)和HN基因全长序列分析。抗原表位分析结果显示,27个鸭分离株均能与其中一株单抗C3-B7反应,而与另外一株单抗1E5反应为阴性。F基因(374bp)序列分析结果显示,4个鸭分离株均属于NDV ClassⅠ分支,分离株之间核苷酸同源性为99.2%~100%;分离株与NDV ClassⅡ毒株遗传距离为0.9%~9.9%,与NDV ClassⅠ毒株遗传距离为38.5%~41.7%。根据核苷酸序列推导的氨基酸序列表明,4个鸭NDV分离株F蛋白裂解位点氨基酸模式为:112-EROERL-117。HN基因序列分析结果显示,4个鸭NDV分离株HN基因全长1851bp,编码585个氨基酸;同源性比较发现4个鸭NDV分离株之间核苷酸同源性为99.7%~99.8%,与NDV ClassⅡ毒株核苷酸同源性为68.4%~70.5%,与NDV ClassⅠ毒株核苷酸同源性为95.8%~98.0%。本研究结果显示,鸭分离毒均属于NDV ClassⅠ弱毒,在抗原表位和基因序列上与广泛应用的NDV弱毒疫苗株(LaSota)不同,这些毒株的来源有待进一步深入研究。

关 键 词:  新城疫病毒  抗原表位  遗传演化

Antigenic epitope and phylogenetia analysis of Newcastle disease virus isolated from ducks
HU Bei-xia,HUANG Yan-yan,LU Xi-shan,ZHANG Xiu-mei,XU Chuan-tian,YAN Shi-gan,ZHANG Wei.Antigenic epitope and phylogenetia analysis of Newcastle disease virus isolated from ducks[J].Chinese Journal of Veterinary Science,2010,30(2).
Authors:HU Bei-xia  HUANG Yan-yan  LU Xi-shan  ZHANG Xiu-mei  XU Chuan-tian  YAN Shi-gan  ZHANG Wei
Abstract:Twenty seven NDV isolates were recovered from tracheal and cloacal swabs of clinically healthy ducks in a scaled farm. Two HN monoclonal antibodies(MAbs) were used to analyze the antigenic epitope of these isolates. The HN gene and the variable region of F gene (47-420 bp) of four isolates were sequenced. All the isolates were recog-nized by MAb C3-B7 in HI test, but the reactions were negative between these isolates and the MAb1E5. Based upon phylogenetic analysis of a 374 bp region of F gene,four isolates related to lentogenic class Ⅰ viruses,with nucleotide sequences identities of 99.2%-100%. There were 0.9%-9.9% nucleotide differences between the isolates and other class Ⅰ virus,whereas there were 38.5%-41.7% nucleotide differences between the isolates and classⅡ viruses. The amino acid sequences of the F protein cleavage sites in these isolates were 112-ERQERL-117. The full length of HN gene of these isolates was 1 851 bp,coding 585 amino acids. The homology analysis of the nucleotide sequence of HN gene indicated that there were 2.0%-4.2% nucleotide differences between the isolates and other class Ⅰ viru-ses,whereas there were 29.5%-31.6% differences between the isolates and class Ⅱ viruses. The results shows that these isolates do not appear to be phylogenetically related to the vaccine strain(LaSota) and further work should be done to find the source of these isolates.
Keywords:duck  Newcastle disease virus  antigenic epitope  phylogenetic analysis
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