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Grapevine virus A variants of group II associated with Shiraz disease in South Africa are present in plants affected by Australian Shiraz disease, and have also been detected in the USA

机译:葡萄病毒南非与设拉子病相关的II组变种存在于受澳大利亚设拉子病影响的植物中,并且在美国也有检测到。

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摘要

Primers were designed for RT-nested PCR amplification of the highly variable 293-nt fragment from the 5′ terminal part of the Grapevine virus A (GVA) replicase gene, specific to South African variants of molecular groups I and II. This new technique, along with RT-PCR for simultaneous amplification of variants of groups I, II and III, as well as cloning of amplicons, single-strand conformation polymorphism (SSCP) analysis of clones and sequencing, were used to investigate the populations of variants infecting 16 local Shiraz grapevines with different Shiraz disease (SD) status. The techniques were also used to study variants in GVA-infected grapevines from Australia and the USA. The Australian grapevines included seven plants of cvs Shiraz and Merlot affected by Australian Shiraz disease (AuSD), and one plant of cv. Crimson Seedless with unknown AuSD status. Grapevines from the USA included plants of cvs Chardonnay, Thompson Seedless and an unknown cultivar. The results confirmed the association of certain genetic variants of group II with SD and showed the common presence of these variants in AuSD-affected grapevines from Australia. Interestingly, a variant of this group was also detected in grapevine cv. Chardonnay from the USA, although the disease has not yet been reported from that country. The study also supports an earlier observation that members of group II, closely related to variant GTR1-2, are not associated with the disease. The variants were found only in SD-free grapevines. Results show that variants of the most divergent group III, which are common in South Africa, are also present in Australia and the USA. These variants are not associated with SD, but frequently occur in mixed infections with members of group II in plants affected by this disease in South Africa.
机译:设计引物用于RT嵌套PCR扩增来自葡萄病毒A(GVA)复制酶基因5'末端部分的高度可变的293-nt片段,该片段对分子组I和II的南非变种具有特异性。这项新技术与RT-PCR一起用于同时扩增I,II和III组的变体,以及克隆扩增子,克隆的单链构象多态性(SSCP)分析和测序,被用于研究A.变种感染了16种具有不同设拉子病(SD)状况的当地设拉子葡萄。该技术还用于研究来自澳大利亚和美国的GVA感染葡萄树的变异。澳大利亚的葡萄树包括受澳大利亚设拉子病(AuSD)影响的七叶树设拉子和梅洛葡萄。深红色无核,具有未知的AuSD状态。来自美国的葡萄藤包括霞多丽(Chardonnay),汤普森无核(Thompson Seedless)和不明品种的植物。结果证实了II组某些遗传变异与SD的关联,并表明这些变异在澳大利亚AuSD影响的葡萄中普遍存在。有趣的是,在葡萄cv中也检测到了该组的变体。来自美国的霞多丽,尽管该国尚未报告该病。该研究还支持较早的观察,即与变体GTR1-2密切相关的II组成员与该疾病​​无关。仅在不含SD的葡萄树中发现了这些变体。结果表明,在南非常见的第三类差异最大的变体也存在于澳大利亚和美国。这些变体与SD无关,但经常在南非受该病影响的植物中与II族成员混合感染时发生。

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  • 作者

    Goszczynski, D.; Habili, N.;

  • 作者单位
  • 年度 2012
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  • 原文格式 PDF
  • 正文语种 en
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  • 入库时间 2022-08-20 21:03:08

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