Morán Félix, Olmos Antonio, Glasa Miroslav, Silva Marilia Bueno Da, Maliogka Varvara, Wetzel Thierry, Ruiz-García Ana Belén
Centro de Protección Vegetal y Biotecnología, Instituto Valenciano de Investigaciones Agrarias (IVIA), Ctra. Moncada-Náquera km 4.5, Moncada, 46113 Valencia, Spain.
Biomedical Research Center of the Slovak Academy of Sciences, Institute of Virology, Dúbravská Cesta 9, 84505 Bratislava, Slovakia.
Plants (Basel). 2023 Feb 15;12(4):876. doi: 10.3390/plants12040876.
Grapevine ( L.) is one of the most important crops in the world due to its economic and social impact. Like many other crops, grapevine is susceptible to different types of diseases caused by pathogenic microorganisms. Grapevine leafroll-associated virus 1 (GLRaV-1) is a virus associated with grapevine leafroll disease and it is considered at the national and European level as a pathogen that must be absent in propagative plant material. For this reason, the availability of specific, sensitive and reliable detection techniques to ascertain the sanitary status of the plants is of great importance. The objective of this research was the development of a new GLRaV-1 detection method based on a TaqMan quantitative real-time RT-PCR targeted to the coat protein genomic region and including a host internal control in a duplex reaction. To this end, three new GLRaV-1 full genomes were recovered by HTS and aligned with all sequences available in the databases. The method has been validated following EPPO standards and applied for the diagnosis of field plant material and transmission vectors. The new protocol designed has turned out to be highly sensitive as well as much more specific than the current available methods for the detection and absolute quantitation of GLRaV-1 viral titer.
葡萄(Vitis vinifera L.)因其经济和社会影响,是世界上最重要的作物之一。与许多其他作物一样,葡萄易受病原微生物引起的不同类型病害的影响。葡萄卷叶相关病毒1(GLRaV-1)是一种与葡萄卷叶病相关的病毒,在国家和欧洲层面,它被视为繁殖性植物材料中必须不存在的病原体。因此,拥有特定、灵敏且可靠的检测技术以确定植物的健康状况至关重要。本研究的目的是开发一种基于TaqMan定量实时RT-PCR的新GLRaV-1检测方法,该方法针对外壳蛋白基因组区域,并在双重反应中包含宿主内参。为此,通过高通量测序(HTS)获得了三个新的GLRaV-1全基因组,并与数据库中所有可用序列进行了比对。该方法已按照欧洲和地中海植物保护组织(EPPO)标准进行了验证,并应用于田间植物材料和传播媒介的诊断。所设计的新方案已证明具有高度灵敏性,并且在检测和绝对定量GLRaV-1病毒滴度方面比目前可用的方法更具特异性。