Agricultural Research Institute, Nicosia 1516, Cyprus.
J Virol Methods. 2010 May;165(2):238-45. doi: 10.1016/j.jviromet.2010.02.003. Epub 2010 Feb 11.
During the past four decades, Tomato yellow leaf curl disease has become one of the major constraints in tomato production worldwide. In the Mediterranean basin, several isolates from two major Begomovirus species are involved in outbreaks and persistent epidemics. A real-time TaqMan PCR assay was developed and evaluated for the rapid and multiplex detection and differentiation of two begomoviruses often found in mixed infections in the region, Tomato yellow leaf curl virus (TYLCV) and Tomato yellow leaf curl Sardinia virus (TYLCSV). This assay was 1000-fold more sensitive than conventional PCR assays described previously, allowing the use of simple template preparation methods and eliminating the need for total nucleic acid purification. The viral DNA template was obtained by spotting sap extract derived from TYLCV or TYLCSV infected tissues on a nylon membrane or by directly using crude plant extracts in the real-time reaction cocktail. Preliminary results showed that this method can successfully detect and discriminate virus species from infected tomato, bean, pepper and different weed species obtained from the Mediterranean basin, the USA and Japan, allowing the simple, fast and cost-effective testing of a large number of samples in certification schemes. The assay can also be used for the detection of these two begomovirus species in their whitefly vector biotypes of the Bemisia tabaci (Gennadius) species group.
在过去的四十年中,番茄黄化曲叶病已成为全球番茄生产的主要限制因素之一。在地中海盆地,两种主要的曲叶病毒种的几个分离株参与了暴发和持续流行。本文开发并评估了一种实时 TaqMan PCR 检测方法,用于快速和多重检测及区分该地区常发生混合感染的两种曲叶病毒,即番茄黄化曲叶病毒(TYLCV)和番茄黄化曲叶撒丁岛病毒(TYLCSV)。该检测方法比之前描述的常规 PCR 检测方法灵敏 1000 倍,允许使用简单的模板制备方法,并且无需进行总核酸纯化。病毒 DNA 模板是通过将 TYLCV 或 TYLCSV 感染组织的汁液点样到尼龙膜上,或直接在实时反应混合物中使用粗制植物提取物来获得的。初步结果表明,该方法可以成功检测和区分来自地中海盆地、美国和日本的受感染番茄、豆类、辣椒和不同杂草物种中的病毒种类,允许在认证计划中对大量样本进行简单、快速和具有成本效益的测试。该检测方法还可用于检测烟粉虱(Bemisia tabaci (Gennadius)种组)传毒生物型中的这两种曲叶病毒。