首页> 外文期刊>Journal of Virological Methods >Differentiation of Tomato yellow leaf curl virus and Tomato yellow leaf curl Sardinia virus using real-time TaqManReg. PCR.
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Differentiation of Tomato yellow leaf curl virus and Tomato yellow leaf curl Sardinia virus using real-time TaqManReg. PCR.

机译:使用实时TaqManReg区分番茄黄叶卷曲病毒和番茄黄叶卷曲撒丁岛病毒。 PCR。

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摘要

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 TaqManReg. 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.
机译:在过去的四十年中,番茄黄叶卷曲病已成为全球番茄生产的主要制约因素之一。在地中海盆地,来自两种主要的乞B病毒的几种分离株参与了暴发和持续流行。实时TaqManReg。开发并评估了PCR检测方法,以快速,多重检测和区分在该地区混合感染中常见的两种番茄病毒,这两种病毒分别是:番茄黄叶卷曲病毒(TYLCV)和番茄黄叶卷曲撒丁岛病毒(TYLCSV)。该测定法的灵敏度比之前所述的常规PCR测定法高1000倍,从而允许使用简单的模板制备方法,并且无需进行总核酸纯化。通过将来源于TYLCV或TYLCSV感染组织的汁液提取物点在尼龙膜上,或直接在实时反应混合物中直接使用粗植物提取物,获得病毒DNA模板。初步结果表明,该方法可以成功地检测和区分感染的番茄,豆类,胡椒和地中海盆地,美国和日本的不同杂草物种中的病毒物种,从而可以简单,快速且经济高效地对大量的病毒进行检测认证计划中的样本。该测定法还可以用于检测烟粉虱(Bemisia tabaci)(Gennadius)物种组的粉虱载体生物型中的这两种begomovirus物种。

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