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利用PCR技术检测草莓镶脉病毒
引用本文:隋春,吴禄平,张志宏.利用PCR技术检测草莓镶脉病毒[J].园艺学报,2003,30(1):82-84.
作者姓名:隋春  吴禄平  张志宏
作者单位:(沈阳农业大学园艺学院, 沈阳110161 )
基金项目:辽宁省自然科学基金项目 ( 9910 10 0 3 0 3 )
摘    要: 采用特异引物的PCR 扩增方法, 对30 个草莓品种进行了草莓镶脉病毒的检测, 同时用指示植物小叶嫁接法对被检植株进行了病毒检测, 两种方法结果一致。回收、克隆PCR 扩增出的特异DNA 片段,获得了携有草莓镶脉病毒CP 基因片段的载体。测序结果表明, 得到的特异DNA 片段同美国草莓镶脉病毒的株系ATCC 45058 CP 基因片段相比, 同源性为90. 94 %。

关 键 词:草莓  草莓镶脉病毒  检测  PCR
文章编号:0513-353X(2003)01-0082-03
收稿时间:2001-12-2
修稿时间:2001年12月2日

Detection of Strawberry Vein Banding Virus in Strawberries by PCR
Sui Chun,Wu Luping,and Zhang Zhihong.Detection of Strawberry Vein Banding Virus in Strawberries by PCR[J].Acta Horticulturae Sinica,2003,30(1):82-84.
Authors:Sui Chun  Wu Luping  and Zhang Zhihong
Institution:( College of Horticulture , Shenyang Agricultural University , Shenyang 110161 , China)
Abstract:Total DNA, isolated from 30 strawberry cultivars, was used as template to amplify strawberry vein banding virus (SVBV) CP gene fragment by polymerase chain reaction (PCR). Meanwhile, the tested plants were detected by indicator leaf grafting technique. The plants with typical band in PCR showed vein banding symptoms in indicator UC5 ( Fragaria vesca ), EMC ( F. vesca ), and those without typical band didn't showed symptoms. Results were identical in two detection methods. The amplified fragment by PCR was recycled, cloned in pMD18 T vector, and then sequenced. It is suggested that the expected SVBV CP gene fragment was obtained and is 90.94 % identical to that of American isolate ATCC 45058.
Keywords:Strawberry  Strawberry vein banding virus (SVBV)  Detection  PCR
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