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Characterization of grapevine leafroll-associated virus 3 genetic variants and application towards RT-qPCR assay design

机译:葡萄叶卷相关病毒3遗传变异的表征及其在RT-qPCR检测设计中的应用

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摘要

Grapevine leafroll-associated virus 3 (GLRaV-3) is the most widely prevalent and economically important of the complex of RNA viruses associated with grapevine leafroll disease (GLD). Phylogenetic studies have grouped GLRaV-3 isolates into nine different monophyletic groups and four supergroups, making GLRaV-3 a genetically highly diverse virus species. In addition, new divergent variants have been discovered recently around the world. Accurate identification of the virus is an essential component in the management and control of GLRaV-3; however, the diversity of GLRaV-3, coupled with the limited sequence information, have complicated the development of a reliable detection assay. In this study, GLRaV-3 sequence data available in GenBank and those generated at Foundation Plant Services, University of California-Davis, was used to develop a new RT-qPCR assay with the capacity to detect all known GLRaV-3 variants. The new assay, referred to as FPST, was challenged against samples that included plants infected with different GLRaV-3 variants and originating from 46 countries. The FPST assay detected all known GLRaV-3 variants, including the highly divergent variants, by amplifying a small highly conserved region in the 3’ untranslated terminal region (UTR) of the virus genome. The reliability of the new RT-qPCR assay was confirmed by an enzyme linked immunosorbent assay (ELISA) that can detect all known GLRaV-3 variants characterized to date. Additionally, three new GLRaV-3 divergent variants, represented by four isolates, were identified using a hierarchical testing process involving the FPST assay, GLRaV-3 variant-specific assays and high-throughput sequencing analysis. These variants were distantly related to groups I, II, III, V, VI, VII and IX, but much similar to GLRaV-3 variants with no assigned group; thus, they may represent new clades. Finally, based on the phylogenetic analysis, a new GLRaV-3 subclade is proposed and named as group X.
机译:葡萄卷叶病相关病毒3(GLRaV-3)是与葡萄卷叶病(GLD)相关的RNA病毒复合物中最广泛流行和经济上重要的。系统发育研究已将GLRaV-3分离株分为九个不同的单系统组和四个超组,从而使GLRaV-3成为遗传上高度多样的病毒种类。另外,最近在世界范围内发现了新的不同变体。在GLRaV-3的管理和控制中,准确识别病毒是必不可少的组成部分。但是,GLRaV-3的多样性以及有限的序列信息使可靠的检测方法的开发变得复杂。在这项研究中,GenBank中提供的GLRaV-3序列数据以及加利福尼亚大学戴维斯分校的基础植物服务部门生成的GLRaV-3序列数据被用于开发一种能够检测所有已知GLRaV-3变体的新型RT-qPCR分析方法。这项新的测定方法称为FPST,对来自包括46个国家的被不同GLRaV-3变体感染的植物的样品提出了挑战。 FPST分析通过扩增病毒基因组3'非翻译末端区域(UTR)中的一个小的高度保守区域来检测所有已知的GLRaV-3变体,包括高度趋异的变体。新的RT-qPCR检测方法的可靠性通过酶联免疫吸附测定(ELISA)得以证实,该酶联免疫吸附测定可以检测迄今已表征的所有已知GLRaV-3变体。此外,使用涉及FPST测定,GLRaV-3特异性变体测定和高通量测序分析的分级测试过程,鉴定了由四个分离物代表的三个新的GLRaV-3趋异变体。这些变体与I,II,III,V,VI,VII和IX密切相关,但与没有指定组的GLRaV-3变体非常相似。因此,它们可能代表新的进化论。最后,在系统发育分析的基础上,提出了一个新的GLRaV-3子小节,并命名为X组。

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