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一种用于检测油菜(甘蓝型油菜)中核盘菌的定量PCR系统。

A Quantitative PCR System for Measuring Sclerotinia sclerotiorum in Canola (Brassica napus).

作者信息

Ziesman B R, Turkington T K, Basu U, Strelkov S E

机构信息

Department of Agricultural, Food and Nutritional Science, University of Alberta, Edmonton, AB, T6G 2P5, Canada.

Lacombe Research Centre, Agriculture and Agri-Food Canada, Lacombe, AB, T4L 1W1, Canada.

出版信息

Plant Dis. 2016 May;100(5):984-990. doi: 10.1094/PDIS-05-15-0605-RE. Epub 2016 Feb 25.

Abstract

Sclerotinia stem rot, caused by Sclerotinia sclerotiorum, is an economically important disease of canola (Brassica napus) commonly managed by routine application of fungicides. Petal infestation has been demonstrated to be an important stage of the disease cycle in canola and has been the focus of previously developed Sclerotinia stem rot risk assessment methods. Quantitative polymerase chain reaction (qPCR) analysis can provide a more rapid and accurate assessment of petal infestation levels. Primers and a hydrolysis probe were designed to amplify a 70-bp region of an S. sclerotiorum-specific gene, SS1G_00263. A hydrolysis probe-based qPCR assay was developed that had a detection limit of 8.0 × 10 ng of S. sclerotiorum DNA and only amplified S. sclerotiorum DNA. Evaluation of petals collected at five sampling points in each of 10 commercial canola fields on each of two sampling dates (corresponding to 20 to 30% bloom and 40 to 50% bloom) revealed S. sclerotiorum DNA infestation levels of 0 to 3.3 × 10 ng/petal. This qPCR assay can be used to reliably quantify petal infestation and, with further research, has the potential to serve as the basis for a Sclerotinia stem rot risk assessment tool or as a means to study Sclerotinia stem rot epidemiology.

摘要

由核盘菌引起的油菜菌核病是油菜(甘蓝型油菜)的一种具有经济重要性的病害,通常通过常规施用杀菌剂来防治。花瓣侵染已被证明是油菜病害循环中的一个重要阶段,并且一直是先前开发的油菜菌核病风险评估方法的重点。定量聚合酶链反应(qPCR)分析可以提供对花瓣侵染水平更快速准确的评估。设计了引物和水解探针以扩增核盘菌特异性基因SS1G_00263的一个70 bp区域。开发了一种基于水解探针的qPCR检测方法,其检测限为8.0×10 ng核盘菌DNA,并且仅扩增核盘菌DNA。在两个采样日期(分别对应于20%至30%开花期和40%至50%开花期)对10个商业油菜田中的每一个在五个采样点采集的花瓣进行评估,结果显示核盘菌DNA侵染水平为0至3.3×10 ng/花瓣。这种qPCR检测方法可用于可靠地量化花瓣侵染情况,并且经过进一步研究,有潜力作为油菜菌核病风险评估工具的基础或作为研究油菜菌核病流行病学的一种手段。

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