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大豆疫霉和桑氏疫霉根腐病病原菌的qPCR和RPA属特异性及种特异性检测方法的开发与应用

Development and Application of qPCR and RPA Genus- and Species-Specific Detection of Phytophthora sojae and P. sansomeana Root Rot Pathogens of Soybean.

作者信息

Rojas J Alejandro, Miles Timothy D, Coffey Michael D, Martin Frank N, Chilvers Martin I

机构信息

Department of Plant, Soil and Microbial Sciences, Michigan State University, East Lansing, 48824; and Program in Ecology, Evolutionary Biology and Behavior, Michigan State University, East Lansing, 48824.

School of Natural Sciences, California State University, Monterey Bay, Seaside, 93955.

出版信息

Plant Dis. 2017 Jul;101(7):1171-1181. doi: 10.1094/PDIS-09-16-1225-RE. Epub 2017 May 15.

DOI:10.1094/PDIS-09-16-1225-RE
PMID:30682964
Abstract

Phytophthora root rot of soybean, caused by Phytophthora sojae, is one of the most important diseases in the Midwestern United States, and is estimated to cause losses of up to 1.2 million metric tons per year. Disease may also be caused by P. sansomeana; however, the prevalence and damage caused by this species is not well known, partly due to limitations of current diagnostic tools. Efficient, accurate, and sensitive detection of pathogens is crucial for management. Thus, multiplex qPCR and isothermal RPA (recombinase polymerase amplification) assays were developed using a hierarchical approach to detect these Phytophthora spp. The assays consist of a genus-specific probe and two species-specific probes that target the atp9-nad9 region of the mitochondrial genome that is highly specific for the genus Phytophthora. The qPCR approach multiplexes the three probes and a plant internal control. The RPA assays run each probe independently with a plant internal control multiplexed in one amplification, obtaining a result in as little as 20 mins. The multicopy mitochondrial genome provides sensitivity with sufficient variability to discern among different Phytophthora spp. The assays were highly specific when tested against a panel of 100 Phytophthora taxa and range of Pythium spp. The consistent detection level of the assay was 100 fg for the qPCR assay and 10 pg for the RPA assay. The assays were validated on symptomatic plants collected from Michigan (U.S.) and Ontario (Canada) during the 2013 field season, showing correlation with isolation. In 2014, the assays were validated with samples from nine soybean producing states in the U.S. The assays are valuable diagnostic tools for detection of Phytophthora spp. affecting soybean.

摘要

由大豆疫霉引起的大豆疫霉根腐病是美国中西部最重要的病害之一,据估计每年造成的损失高达120万吨。该病害也可能由桑氏疫霉引起;然而,由于目前诊断工具的局限性,该物种的流行情况和造成的损害尚不明确。对病原体进行高效、准确和灵敏的检测对于病害管理至关重要。因此,采用分层方法开发了多重定量聚合酶链反应(qPCR)和等温重组酶聚合酶扩增(RPA)检测方法,以检测这些疫霉属物种。这些检测方法由一个属特异性探针和两个物种特异性探针组成,靶向线粒体基因组的atp9-nad9区域,该区域对疫霉属具有高度特异性。qPCR方法将这三种探针与一个植物内参进行多重检测。RPA检测方法则将每个探针独立运行,并在一次扩增中与一个植物内参进行多重检测,最短20分钟即可获得结果。多拷贝的线粒体基因组提供了灵敏度,且具有足够的变异性以区分不同的疫霉属物种。当针对100个疫霉分类群和一系列腐霉属物种进行测试时,这些检测方法具有高度特异性。qPCR检测方法的一致检测水平为100 fg,RPA检测方法为10 pg。在201年田间季节从美国密歇根州和加拿大安大略省采集的有症状植株上对这些检测方法进行了验证,结果显示与分离结果具有相关性。2014年,在美国9个大豆生产州的样本上对这些检测方法进行了验证。这些检测方法是检测影响大豆的疫霉属物种的有价值的诊断工具。

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