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鹅副粘病毒YG97分离株HN蛋白基因的克隆与序列分析
引用本文:刘华雷,王永坤,朱国强,严维巍.鹅副粘病毒YG97分离株HN蛋白基因的克隆与序列分析[J].中国预防兽医学报,2002,24(5):334-337.
作者姓名:刘华雷  王永坤  朱国强  严维巍
作者单位:1. 江苏省家禽科学研究所,江苏,扬州,225003
2. 扬州大学畜牧兽医学院,江苏,扬州,225009
摘    要:鹅副粘病毒分离株YG97经10日龄鸡胚增殖后纯化,提取病毒的基因组RNA,采用RT-PCR一次性扩增出与预期设计的1.9kb大小相符合的特异性条带。将扩增产物提纯后克隆入pGEM^R-T载体,经转化、筛选及酶切鉴定后,初步获得了含鹅副粘病毒HN基因的阳性克隆,进一步进行了序列测定。序列分析表明所扩增的病毒的HN基因片段的长度为198bp,共编码571个氨基酸。同源性分析表明,YG97与LaSota毒株核苷酸同源性为79%,氨基酸的同源性为87%。与台湾1995年分离株Taiwan/95核苷酸和氨基酸的同源性分别为93%、96%,说明YG97与Taiwan/95亲缘关系较近,具有较高的相似性。与国内外部分发表的其它NDV毒株的核苷酸同源性在80%-84%之间,氨基酸的同源性在87%-91%之间。同源性分析表明YG97相对于经典的NDV在HN基因上发生了较大的变异。

关 键 词:  副粘病毒  YG97分离株  HN蛋白基因  克隆  序列分析
文章编号:1008-0589(2002)05-0334-04
修稿时间:2001年11月24

Cloning and Sequencing of HN Gene of Goose' s Paramyxovirus
LIU Hua-lei ,WANG Yong-kun ,ZHU Guo-qiang ,YAN Wei-wei.Cloning and Sequencing of HN Gene of Goose'' s Paramyxovirus[J].Chinese Journal of Preventive Veterinary Medicine,2002,24(5):334-337.
Authors:LIU Hua-lei  WANG Yong-kun  ZHU Guo-qiang  YAN Wei-wei
Institution:LIU Hua-lei 1,WANG Yong-kun 2,ZHU Guo-qiang 2,YAN Wei-wei 2
Abstract:The genomic RNA of YG 97 were extracted.The hameagglutinin-neuraminidase (HN) gene of YG 97 has been successfully amplified RT-PCR and coloned in to pGEM-T vector.The sequence analysis showed that the nucleotide sequence of the HN gene was 1981 bp and encoding a protein of 571 amino acids.Sequence comparison between YG 97and the Taiwan/95 strains,the homology of the nucleotide was 93%,the homology of the amino acid was 96%,which indicated they probably had a common origin.The homology of the nucleotide compared with LaSota was 79%,the homology of the amino acid was 87%.The results indicated the mutation on the HN gene had varied largely,compared with classic NDH.
Keywords:Goose's Paramyxovirus  Haemagglutinin-neuraminidase gene  Sequenfce analysis  homology
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