摘要
根据大蒜潜隐病毒(garlic latent virus,GLV)和洋葱黄矮病毒(onion yellow dwarf virus,OYDV)的外壳蛋白基因核苷酸序列分别设计2对特异性引物,在单重RT-PCR检测的基础上,建立同时检测GLV和OYDV的多重RT-PCR技术体系.结果表明:该方法可从带病的甘肃‘成县迟蒜’大蒜样品中扩增出GLV(849bp)和OYDV(571bp)的2条特异性片段.GLV扩增产物与GenBank中登录的其他分离物核苷酸同源性在90.00%~99.76%,OYDV扩增产物与其他分离物核苷酸的同源性为90.00%~98.00%.
Tow pairs of specific primer were designed based on the nucleotide sequence of garlic latent virus(GLV) and onion yellow dwarf virus(OYDV) coat protein region.A multiplex RT-PCR system was established to simultaneously detect two viruses of garlic,according to the result of single RT-PCR.All the samples from chengxianchisuan of Gansu infected by GLV and OYDV could be amplified by the multiplex RT-PCR,and yielding two specific bands of GLV(849 bp),OYDV(571 bp).Sequence analysis of the amplified products showed that the nucleotide sequences homology of GLV and OYDV was 90%~99.76% and 90%~98%,respectively compared with the sequences of other isolates in the GenBank..
出处
《甘肃农业大学学报》
CAS
CSCD
北大核心
2013年第2期46-49,54,共5页
Journal of Gansu Agricultural University
基金
甘肃省农牧厅生物技术研究项目(GNSW-2009-07)