摘要
对我国不同来源的狂犬病病毒野毒株8202、BRV、MRV的G基因405~1146位核苷酸序列,进行了逆转录-聚合酶链反应(RT-PCR)扩增、克隆和序列测定,并应用计算机对这3个毒株的测定序列和已发表的中国人源毒株(CGX89)的相应序列进行了分析比较。结果表明,这4个中国不同来源狂犬病病毒的G基因同源性较低,8202与BRV的核苷酸同源性只有79.5%,与MRV的氨基酸同源性亦只有82.2%;同一地区自不同动物分离的MRV株与BRV株其亲缘关系较远。4个野毒株的糖基化位点和主要的诱导中和抗体产生的抗原决定簇内某些氨基酸亦不同,从而证明我国存在亲缘关系较远的狂犬病野毒株。
The fragment from 405nt to 1146 nt of glycoprotein(G) ectodomain gene of rabies virus strains 8202,BRV and MRV,isolated from deer,calf,mouse respectively in various areas of China,were amplified by RT-PCR.Then they were cloned and sequenced by Sanger's dideoxy method.Comparison of nucleotide and deduced amino acid sequences of them and the previously published CGX89 strain (from human) was performed by computer with DNASIS software.The results showed that homology of the nucleotide sequences and the amino acid sequences of four Chinese rabies viruses were very low.Homology of the nucleotide sequence of 8202 with BRV was only 79.5% and homology of amino acid sequence of 8202 with MRV was 82.2%.The fact that homology of BRV with MRV,isolated from different animals in Henan area,was only 81.1% showed that they could not be from the same ancestor.Some amino acids in Ag Ⅱ and Ag Ⅲ sites and potential glycosylation sites of four strains were different.This result proved that rabies viruses from China might be divided into different genotypes.
出处
《病毒学报》
CAS
CSCD
北大核心
1998年第3期262-267,共6页
Chinese Journal of Virology
基金
全军医药卫生科研基金