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新疆三种葡萄病毒RT-PCR检测及序列分析
引用本文:梁巧玲,乾义柯,张娜,陆平,刘绪斌.新疆三种葡萄病毒RT-PCR检测及序列分析[J].植物保护学报,2015,42(3):376-381.
作者姓名:梁巧玲  乾义柯  张娜  陆平  刘绪斌
作者单位:1. 伊犁职业技术学院,新疆伊宁,835000
2. 伊犁出入境检验检疫局,新疆伊宁,835000
3. 伊犁师范学院,新疆伊宁,835000
基金项目:新疆维吾尔自治区科技支疆项目(2013911090)
摘    要:为研究新疆葡萄中沙地葡萄茎痘伴随病毒(Grapevine rupestris stem pitting associated virus,GRSPa V)、葡萄斑点病毒(Grapevine fleck virus,GFk V)及葡萄病毒A(Grapevine virus A,GVA)的发生情况和新疆分离株系统进化关系,分别克隆3种病毒新疆分离株部分基因区域,应用RT-PCR对新疆64份葡萄样品中上述3种病毒进行检测,并进行系统进化分析。结果显示,GRSPa V、GFk V和GVA的检出率分别为31.3%、62.5%和25.0%。新疆GRSPa V分离株(KJ801847)与美国GRSPa V分离株(AY368590)同源性达96.59%;新疆GFk V分离株(KJ801846)与日本GFk V分离株(AB222861)及中国辽宁GFk V分离株(JF927942)的同源性分别为91.70%和91.03%;新疆GVA分离株(KJ801845)与波兰GVA分离株(JN860997)同源性为93.88%,与中国四川GVA分离株(HQ671655)及辽宁GVA分离株(FJ445220)的同源性分别为92.92%和89.53%。表明3种葡萄病毒在新疆发生比较普遍,且新疆分离株与国内其它地方的分离株存在较大差异。

关 键 词:葡萄病毒  RT-PCR检测  序列分析
收稿时间:2014/5/23 0:00:00

RT-PCR detection and sequence analysis on three grapevine viruses from Xinjiang Uyghur Autonomous Region
Liang Qiaoling,Qian Yike,Zhang N,Lu Ping and Liu Xubin.RT-PCR detection and sequence analysis on three grapevine viruses from Xinjiang Uyghur Autonomous Region[J].Acta Phytophylacica Sinica,2015,42(3):376-381.
Authors:Liang Qiaoling  Qian Yike  Zhang N  Lu Ping and Liu Xubin
Institution:Yili Vocational and Technical College, Yining 835000, Xinjiang Uyghur Autonomous Region, China;Yili Entry and Exit Inspection and Quarantine Bureau, Yining 835000, Xinjiang Uyghur Autonomous Region, China;Yili Normal College, Yining 835000, Xinjiang Uyghur Autonomous Region, China;Yili Entry and Exit Inspection and Quarantine Bureau, Yining 835000, Xinjiang Uyghur Autonomous Region, China;Yili Entry and Exit Inspection and Quarantine Bureau, Yining 835000, Xinjiang Uyghur Autonomous Region, China
Abstract:To detect the grape virus, including Grapevine rupestris stem pitting associated virus (GRSPaV), Grapevine fleck virus (GFkV), Grapevine virus A (GVA), and evaluate their phylogenetic relationships with isolates from other geographic origins, the three kinds of virus were detected by RT-PCR in 64 grape samples from Xinjiang and sequenced. The results showed that the positive percentage with GRSPaV, GFkV and GVA were 31.3%, 62.5% and 25.0%, respectively. The GRSPaV isolate (KJ801847) from Xinjiang shared 96.59% identity with USA isolate (AY368590), and GFkV isolate (KJ801846) shared sequence similarity of 91.70% and 91.03% with Japan isolate (AB222861) and Liaoning (China) isolate (JF927942), respectively. GVA isolate (KJ801845) shared 93.88%, 92.92% and 89.53% identity with Poland isolate (JN860997), Sichuan (China) isolate (HQ671655) and Liaoning (China) isolate (FJ445220), respectively. The detection demonstrated that the three grapevine viruses were widespread distributed in Xinjiang with a significant difference from other isolates in China.
Keywords:grapevine virus  RT-PCR detection  sequence analysis
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