Department of Plant Pathology, North Dakota State University, Fargo, ND 58108.
Small Grains and Potato Germplasm Research Unit, USDA-ARS, Aberdeen, ID 83210.
Plant Dis. 2023 Nov;107(11):3344-3353. doi: 10.1094/PDIS-03-23-0439-SR. Epub 2023 Nov 6.
The stubby root nematode is an important plant-parasitic nematode species within the Trichodoridae family. It can directly harm the plants by feeding on the roots or indirectly by transmitting . These nematodes are mostly diagnosed either by traditional microscopic methods or a polymerase chain reaction (PCR)-based method. Droplet digital PCR (ddPCR) is a novel PCR technique which is sensitive and precise in quantifying DNA templates of the test samples. In this study, we developed a ddPCR assay to detect and quantify in soil. The specificity and sensitivity of the assay was first determined using nematode DNA or DNA from sterilized soil artificially inoculated with , and the assay was used to quantify populations in field soils. The assay did not detect nematodes other than , thus showing high specificity. It was able to detect equivalent to a 0.01 and 0.02 portion of a single nematode in soil DNA and nematode DNA extracts, respectively. Highly linear relationships between DNA copy numbers from ddPCR and serial dilutions of known concentrations were observed with DNA from nematodes ( = 0.9842) and from artificially infested soil ( = 0.9464). The populations from field soils determined by ddPCR were highly correlated with traditional microscopic counts ( = 0.7963). To our knowledge, this is the first report of applying ddPCR to detect and quantify stubby root nematode in soil. The results of this study support the potentiality of a ddPCR assay as a new research tool in diagnostics of plant-parasitic nematodes.
短体线虫是指短体属根结线虫,属于滑刃目滑刃科根结线虫属,是一类重要的植物寄生线虫。它们可以直接取食植物根系,也可以通过传播植物病毒间接为害植物。目前,该类线虫主要通过传统的形态学方法或聚合酶链式反应(PCR)方法进行检测。数字 PCR(ddPCR)是一种新型的 PCR 技术,它在定量检测测试样本的 DNA 模板时具有较高的灵敏度和精确性。本研究开发了一种 ddPCR 检测方法,用于检测和定量土壤中的短体线虫。该方法首先通过使用线虫 DNA 或经消毒土壤人工接种短体线虫后的 DNA 来确定检测方法的特异性和灵敏度,然后使用该方法对田间土壤中的短体线虫种群进行定量。该检测方法未检测到除短体线虫以外的其他线虫,表明其具有较高的特异性。该方法在土壤 DNA 和线虫 DNA 提取物中检测到相当于单个线虫的 0.01 和 0.02 拷贝时,具有较高的灵敏度。ddPCR 法获得的 DNA 拷贝数与已知浓度的线虫 DNA( = 0.9842)和人工接种土壤 DNA( = 0.9464)的系列稀释液之间存在高度线性关系。通过 ddPCR 法检测到的田间土壤短体线虫种群与传统的显微镜计数高度相关( = 0.7963)。据我们所知,这是首次报道应用 ddPCR 法检测和定量土壤中的短体线虫。本研究结果支持 ddPCR 检测方法作为一种新的植物寄生线虫诊断研究工具的潜力。