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猪PRRSV云南分离株主要蛋白基因克隆及序列分析 被引量:1

Cloning and Sequence Analysis of Porcine Reproductive and Respiratory Syndrome Virus Major Protein Genes
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摘要 采用RT-PCR技术,分别对PRRSV云南分离株-YN株编码GP3、GP5、M蛋白的基因进行扩增,获得764、602、524 bp特异性目的片段,经纯化后,克隆至pMD18-T载体中,分别进行序列测定与分析。结果表明,云南PRRSV与已知代表毒株核苷酸序列同源性分别为89.72%~98.80%;遗传进化分析表明,云南分离株与HB-2(sh)/2002、CH-1a等毒株关系最近,与VR-2332、respPRRS mlv等同属一个大分支,而与JXA1、GD、NM1等毒株处于不同的分支。 The major protein genes of porcine reproductive and respiratory syndrome virus(PRRSV) YN strains,GP3,GP5 and M,were amplified by RT-PCR,and the special 764bp,602bp and 524 bp fragments were obtained,respectively.The PCR products of GP3,GP5 and M genes were purified and cloned into pMD18-T vector for sequencing and sequence alignment.The results of sequence analysis showed that the homologies of nucleotide of PRRSV genes from Yunnan strains were 89.72%-98.80% with known representative PRRSV strains.The phylogenetic analysis revealed that the YN strain was similar to HB-2(sh)/2002 and CH-1a,etc.YN strain,VR-2332 and respPRRS mlv,etc.belonged to the same group,but the YN strain was not closely related to JXA1,GD,NM1 strains.
出处 《动物医学进展》 CSCD 北大核心 2010年第5期18-22,共5页 Progress In Veterinary Medicine
基金 国家自然科学基金(30960285) 云南省教育厅基金(08C0072) 云南省科技厅基金(2008CD134 2009CD063) 高层次科技人才培引工程基金(2009CI125-13 2009CI125-14)
关键词 猪繁殖与呼吸综合征病毒 基因 克隆 序列分析 PRRSV gene clone sequence analysis
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