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首页> 外文期刊>Plant Pathology >Development of a quantitative real-time PCR assay for Phytophthora infestans and its applicability to leaf, tuber and soil samples
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Development of a quantitative real-time PCR assay for Phytophthora infestans and its applicability to leaf, tuber and soil samples

机译:疫霉疫菌定量实时PCR分析方法的开发及其在叶片,块茎和土壤样品中的适用性

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摘要

A sensitive real-time polymerase chain reaction (PCR) assay was developed for the quantification of Phytophthora infestans, the cause of foliar and tuber late blight in potato. A primer pair (PinfTQF/PinfTQR) and a fluorogenic probe (PinfTQPR) were designed to perform a quantitative assay for the detection of P. infestans in leaves, tubers and soils. The assay was shown to be specific to P. infestans and the very closely taxonomically related non-potato pathogen species P. mirabilis, P. phaseoli and P. ipomoea, but did not detect the potato pathogens P. erythroseptica and P. nicotianae. The assay was able to reliably detect P. infestans DNA at 100 fg per reaction and was effective in quantifying P. infestans in infected leaf tissue from 24 h after inoculation and also in infected symptomless tubers and diseased tubers. Attempts to detect oospores of P. infestans in naturally and artificially infested soil samples are described and compared with baiting tests and previous literature. It was not possible to detect oospores in soil samples due to problems with DNA extraction from the oospores themselves. However, the assay was shown to detect even very low levels of asexual inoculum (sporangia and mycelium) in soil. This work assembles all the necessary features of a quantitative P. infestans assay, which have previously been somewhat disparate: the sensitivity, specificity and quantitation are fully validated, the assay is shown to work in common applications in leaf and tuber tissue and the problems with P. infestans oospore detection are explored and tested experimentally.
机译:开发了一种灵敏的实时聚合酶链反应(PCR)分析法,用于定量检测疫霉疫霉,疫霉是马铃薯叶片和块茎晚疫病的起因。设计引物对(PinfTQF / PinfTQR)和荧光探针(PinfTQPR),以进行定量分析以检测叶片,块茎和土壤中的疫霉菌。该测定法显示出对疫病疫霉和与分类学密切相关的非马铃薯病原菌物种奇异疟原虫,菜豆腐虫和番薯疫病菌具有特异性,但未检测到马铃薯病原体疫霉菌和烟草病原菌。该测定法能够可靠地检测到每反应100 fg的致病疫霉DNA,并有效地定量了接种后24小时后受感染的叶片组织以及受感染的无症状块茎和患病块茎中的致病疫霉。描述了尝试在自然和人工感染的土壤样品中检测致病疫霉的卵菌,并与诱饵试验和以前的文献进行了比较。由于从卵孢子本身提取DNA存在问题,因此无法检测土壤样品中的卵孢子。但是,该检测方法甚至可以检测到土壤中极低水平的无性接种物(孢子囊和菌丝体)。这项工作集结了疫病疫霉定量分析的所有必要功能,这些功能以前曾有所不同:灵敏度,特异性和定量已得到充分验证,该方法在叶和块茎组织中的常见应用以及与进行了P. infestans卵孢子检测的探索和实验测试。

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