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用于同时检测木本作物和环境样品中物种的三重实时定量PCR。

Triplex real-time qPCR for the simultaneous detection of species in woody crops and environmental samples.

作者信息

Romero-Cuadrado Laura, Aguado Ana, Ruano-Rosa David, Capote Nieves

机构信息

Department of Sustainable Crop Protection, Andalusian Institute of Agricultural and Fisheries Research and Training (IFAPA), Seville, Spain.

出版信息

Front Plant Sci. 2024 Oct 11;15:1435462. doi: 10.3389/fpls.2024.1435462. eCollection 2024.

Abstract

INTRODUCTION

Species of fungi are relevant pathogens of almond causing trunk cankers, extensive gumming, necrosis of internal tissues and plant dieback and dead, threatening almond productivity. A novel triplex quantitative real-time PCR (qPCR) assay was designed for the simultaneous detection and quantification of , and the family.

MATERIAL AND METHODS

The method was validated in symptomatic and asymptomatic almond, avocado, blueberry and grapevine plants and in environmental samples, such as cropping soil and rainwater and in artificially inoculated trapped spores, demonstrating the same performance on several matrices.

RESULTS AND DISCUSSION

The limit of detection of the triplex qPCR was 10 fg of genomic DNA for the three fungal targets, with high correlation coefficients (R2) and amplification efficiencies between 90 and 120%. Although the triplex qPCR demonstrated to be more sensitive and accurate than the traditional plate culturing and further sequencing method, a substantial agreement (kappa index = 0.8052 ± 0.0512) was found between the two detection methods. The highly sensitive qPCR assay allows for accurate diagnosis of symptomatic plants and early detection of fungi in asymptomatic plants (rootstocks and grafting scions from almond nurseries). Furthermore, the triplex qPCR successfully detected fungi in environmental samples, such as cropping soils and rainwater. It was also capable of detecting as few as 10 conidia in artificially inoculated tapes. Therefore, the triplex qPCR is a valuable tool for accurate diagnosis, aiding in the implementation of suitable control measures. It enables preventive detection in asymptomatic samples, helping to avoid the introduction and spread of these pathogens in production fields. Moreover, it assists in identifying inoculum sources and quantifying inoculum levels in crop environments, contributing to a precise phytosanitary application schedule, thereby reducing production costs and preserving the environment.

摘要

引言

真菌种类是杏仁的重要病原体,可导致树干溃疡、大量流胶、内部组织坏死以及植株枯死,威胁杏仁产量。设计了一种新型三重定量实时荧光定量聚合酶链反应(qPCR)检测方法,用于同时检测和定量分析[具体真菌名称未给出]以及[具体真菌名称未给出]科。

材料与方法

该方法在有症状和无症状的杏仁、鳄梨、蓝莓和葡萄植株以及环境样本(如种植土壤和雨水)和人工接种的捕获孢子中进行了验证,证明在几种基质上具有相同的性能。

结果与讨论

三重qPCR对三种真菌靶标的检测限为10 fg基因组DNA,具有高相关系数(R2),扩增效率在90%至120%之间。尽管三重qPCR比传统平板培养和进一步测序方法更灵敏、准确,但两种检测方法之间存在高度一致性(kappa指数 = 0.8052 ± 0.0512)。这种高度灵敏的qPCR检测方法能够准确诊断有症状的植株,并早期检测无症状植株(杏仁苗圃的砧木和嫁接接穗)中的[具体真菌名称未给出]真菌。此外,三重qPCR成功检测到环境样本(如种植土壤和雨水)中的[具体真菌名称未给出]真菌。它还能够在人工接种的胶带中检测到低至10个分生孢子。因此,三重qPCR是一种用于准确诊断的有价值工具,有助于实施适当的控制措施。它能够在无症状样本中进行预防性检测,有助于避免这些病原体在生产田间的引入和传播。此外,它有助于识别接种源并量化作物环境中的接种水平,有助于制定精确的植物检疫应用计划,从而降低生产成本并保护环境。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5883/11502354/921988df729a/fpls-15-1435462-g001.jpg

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