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用于灵敏检测和区分马铃薯Y病毒分离株的一步法逆转录实时荧光定量PCR。

Single-step RT real-time PCR for sensitive detection and discrimination of Potato virus Y isolates.

作者信息

Kogovsek P, Gow L, Pompe-Novak M, Gruden K, Foster G D, Boonham N, Ravnikar M

机构信息

National Institute of Biology, Vecna pot 111, SI-1000 Ljubljana, Slovenia.

出版信息

J Virol Methods. 2008 Apr;149(1):1-11. doi: 10.1016/j.jviromet.2008.01.025. Epub 2008 Mar 6.

Abstract

Potato virus Y (PVY) has a worldwide distribution and infects several economically important crops from the Solanaceae family. The emergence and spread of the PVYNTN strain, which is the causative agent of potato tuber necrotic ringspot disease (PTNRD), has lead to large economic losses and highlighted the need for accurate discrimination of the different PVY strains. Detection and differentiation of PVY isolates is mainly based on a combination of ELISA, RT-PCR and bioassays; however, PVYNTN isolates are particularly difficult to differentiate from standard PVYN without the use of time-consuming bioassays. A strong correlation has been identified previously between the ability to induce PTNRD and the presence of a recombination point in the virus coat protein. An RT real-time PCR assay has been developed to enable detection of isolates with the recombination point, therefore, enabling rapid differentiation between potentially tuber necrotic PVYNTN isolates and standard PVYN isolates. The assay is also able to detect the presence of PVYO isolates. To aid with routine testing, immuno-capture and post-ELISA virus release were introduced; when coupled with RT real-time PCR the sensitivity of the assays were up to seven orders of magnitude higher than ELISA. The assay was shown to be a suitable method for rapid large-scale diagnostic testing of PVY in different types of plant material including tubers, and specific screening for potentially tuber necrotic recombinant isolates.

摘要

马铃薯Y病毒(PVY)在全球范围内分布,可感染茄科几种具有重要经济价值的作物。PVYNTN株系是马铃薯块茎坏死环斑病(PTNRD)的病原体,其出现和传播已造成巨大经济损失,并凸显了准确区分不同PVY株系的必要性。PVY分离株的检测和鉴别主要基于酶联免疫吸附测定(ELISA)、逆转录聚合酶链反应(RT-PCR)和生物测定法的联合使用;然而,如果不使用耗时的生物测定法,PVYNTN分离株与标准PVYN分离株特别难以区分。先前已确定诱导PTNRD的能力与病毒外壳蛋白中重组点的存在之间存在密切关联。因此,已开发出一种逆转录实时聚合酶链反应测定法,用于检测具有重组点的分离株,从而能够快速区分潜在的块茎坏死PVYNTN分离株和标准PVYN分离株。该测定法还能够检测PVYO分离株的存在。为了便于常规检测,引入了免疫捕获和酶联免疫吸附测定后病毒释放法;当与逆转录实时聚合酶链反应结合使用时,这些测定法的灵敏度比酶联免疫吸附测定法高出多达七个数量级。该测定法被证明是一种适用于对包括块茎在内的不同类型植物材料中的PVY进行快速大规模诊断检测以及对潜在的块茎坏死重组分离株进行特异性筛选的方法。

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