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牛病毒性腹泻病毒长春分离株P125基因的克隆与序列测定
Cloning and sequencing of P125 gene of bovineviral diarrhea virus NCD strain
【摘要】 以MDBK细胞培养致细胞病变型牛病毒性腹泻病毒 (BVDV)NCD毒株 ,采用异硫氰酸胍一步法提取总RNA ,并根据BVDVNADL参考株序列设计合成的 1对引物 (W 1与W 2 ) ,进行反转录PCR (RT PCR) ,扩增出P12 5基因区约40 0bp的片段。经 pGEM T载体连接后克隆、测序 ,并与已发表的NADL、Osloss、SD 1、184、D、H、Yak等BVDV毒株序列进行比较。结果表明 :NCD株P12 5基因区无插入或缺失变异 ,但存在着核苷酸的替换 ;经聚类分析初步认为NCD株属于Ⅰa型。NCD株与长春 184、H株核苷酸序列差异较大 ,而亲缘关系较近 ,表明BVDV在同一地区存在不同进化来源的毒株
【Abstract】 CytopathicbovineviraldiarrheavirusNCDstrainwaspropagatedintheMDBKcellandthecelltotalRNAisextractedby single stepmethodofacidguanidiniumthiocyanate phenol chloroformextraction .Afragmentofapproximately 40 0bpwasamplifiedbyre versetranscription polymerasechainreaction(RT PCR)withapairofprimersW 1/W 2 ,whichweredesignatedandsynthesizedbasedonthe publishedsequenceofreferencestrainNADL .ThefragmentwasclonedviapGEM Tvectorandsequenced ,thenthesequencewascompari sonwiththeBVDVNADL ,Osloss ,SD 1,184,H ,DandYakstrains .TheresultconfirmsthatNCDstrain ,likecivilstrains 184,H ,D , Yak ,doesnotpossessanyinsertionordeletionintheP12 5 generegion .Butnucleotideandaminoacidsubstitutionswerefoundinthese quenceanalysed ,whichdiffersfromNADL ,Osloss ,SD 1strains.ThesequenceandaminoacidhomologyofNCDwithgenotypeIaDstrains isthehighest ,98.1%and 97.7%respectively ;whilewithNADLare 82 .0 %and93 .0 % ,soitbelongstogenotypeIabydendrogram analysis .ButthereweremuchdifferencebetweenthesequenceofNCDand 184orHChangchunisolates ,andthethreestrainsshowhigh geneticrelation ,whichrevealedthattherewerestrainsfromdifferentgeneticorigininthesameregion .
- 【文献出处】 中国兽医科技 ,Chinese Journal of Veterinary Science and Technology , 编辑部邮箱 ,2001年02期
- 【分类号】S858.23
- 【被引频次】27
- 【下载频次】146