IF 4.4 2区 农林科学 Q1 PLANT SCIENCES
Lexi Heger, Nancy Sharma, Austin Glenn McCoy, Frank N Martin, Laura Avila Miles, Martin I Chilvers, Rachel P Naegele, Timothy D Miles
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引用次数: 0

摘要

在葡萄园中,由卵菌病原体葡萄霜霉病菌(Plasmopara viticola)引起的葡萄霜霉病如果不加以防治,会造成重大经济损失。葡萄霜霉病菌是一个物种复合体,由至少四个支系或隐性物种组成,在葡萄科至少八种植物上致病。在美国,aestivalis、riparia 和 vinifera 支系已被确定存在于五大湖区的栽培葡萄上。在本研究中,利用 Plasmopara 物种特有的线粒体基因顺序差异(cox1-atp1),开发了能够区分这三个类群的多重 TaqMan qPCR 检测系统。在研究这些类群与其不同寄主之间的关系以及杀真菌剂抗性发展的过程中,需要用这种检测方法来明确区分近缘种。使用不同类型的目标样本和非目标样本(包括叶片、ToughSpot 贴纸和空气采样棒)对多重化验进行了验证。该检测方法还转移到了数字 PCR(dPCR)平台上并在该平台上进行了优化。使用 qPCR 和 dPCR 检测法对空气采样棒和人工接种的混合样本进行了测试,以评估每种检测法的效用。每个支系的多重检测显示出不同的灵敏度,qPCR 的灵敏度为 10 到 1,000 fg DNA,效率为 70-85%。dPCR 的灵敏度相同,只有riparia 支系的灵敏度可能提高 10 倍。这些结果表明,在尝试诊断植物病原体时,dPCR 可以作为比 qPCR 更灵敏的选择,但这取决于检测方法。该检测系统可检测病原体并对葡萄孢菌支系进行分类,从而在种植多种栽培葡萄或野生葡萄的地区进行鉴别。由于野生寄主有可能携带不同的葡萄霜霉病菌支系,而商业葡萄园对霜霉病菌的管理非常严格,因此该系统将继续发挥重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multiplexed real-time and digital PCR tools to differentiate clades of Plasmopara viticola causing downy mildew in grapes.

In vineyards, downy mildew of grapes, caused by the oomycete pathogen Plasmopara viticola, can cause significant economic losses when left unmanaged. P. viticola is a species complex, made up of at least four clades, or cryptic species, causing disease on at least eight plant species within the family Vitaceae. In the United States, clades aestivalis, riparia, and vinifera, have been identified, as being present in the Great Lakes region on cultivated grapes. Within this study, a multiplexed TaqMan qPCR assay system capable of differentiating among these three taxa was developed using a mitochondrial gene order difference unique to Plasmopara species (cox1-atp1). The assay is needed to clearly differentiate among the closely related species as research investigates relationships between the clades and their varying hosts as well as fungicide resistance development. The multiplexed assay was validated using a panel of target and non-target samples of varying types, including leaves, ToughSpot stickers, and air sampling rods. The assay was also transferred to and optimized on a digital PCR (dPCR) platform. Air sampling rods and artificially inoculated mixed samples were tested using both qPCR and the dPCR assays to gauge utility of each. The multiplexed assays for each clade showed varying sensitivity of 10 to 1,000 fg of DNA and efficiency of 70-85% in qPCR. The dPCR sensitivity was the same, except for clade riparia, which showed a potential tenfold increase in sensitivity. These results suggest that the dPCR can serve as a more sensitive option than qPCR when trying to diagnose plant pathogens, but it is dependent on the assay. This assay system provides detection of the pathogen and classification of P. viticola clades allowing discrimination in areas growing multiple cultivated or wild grape species. This will continue to be relevant as wild hosts can potentially harbor different P. viticola clades and downy mildew is intensely managed in commercial vineyards.

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来源期刊
Plant disease
Plant disease 农林科学-植物科学
CiteScore
5.10
自引率
13.30%
发文量
1993
审稿时长
2 months
期刊介绍: Plant Disease is the leading international journal for rapid reporting of research on new, emerging, and established plant diseases. The journal publishes papers that describe basic and applied research focusing on practical aspects of disease diagnosis, development, and management.
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