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用于快速检测大豆上新发现的根腐线虫的重组酶聚合酶扩增检测方法的开发。

Development of a Recombinase Polymerase Amplification Assay for Rapid Detection of the New Root-Lesion Nematode on Soybean.

作者信息

Dhakal Roshan, Chowdhury Intiaz Amin, Plaisance Addison, Yan Guiping

机构信息

Department of Plant Pathology, North Dakota State University, Fargo, ND 58108, U.S.A.

出版信息

Plant Dis. 2025 Mar;109(3):603-614. doi: 10.1094/PDIS-05-24-1133-RE. Epub 2025 Feb 28.

DOI:10.1094/PDIS-05-24-1133-RE
PMID:39320378
Abstract

Root-lesion nematodes, spp., are reported to cause serious yield losses in various crops, including soybean. A new root-lesion nematode species was detected in 2015 in a soybean field in North Dakota (ND) and named in 2021. Nematode detection and differentiation from other species are critical in management strategies. Thus, a recombinase polymerase amplification (RPA) assay was developed for rapid detection of this nematode from field soils under isothermal conditions. New primers and probes were designed from internal transcribed spacer-ribosomal DNA region of the nematode genome and tested for both specificity and sensitivity. The RPA assay was able to detect DNA from a single adult nematode at 39.5°C in 20 min using both TwistAmp Basic and Exo Kits. The specificity of the primers was initially confirmed through in silico analyses and followed by laboratory tests. The assay successfully amplified DNA from the target species, although no amplification occurred for other spp. and non- control species. Sensitivity testing with real-time RPA revealed its ability to detect DNA in dilutions equivalent to 1/32 of a single nematode from DNA extracted from inoculated sterile soil. To further validate the assay, it was tested with 19 field soil samples collected in ND. This assay amplified soil DNA extracts of all -infested field samples confirmed through conventional PCR. It did not amplify DNA from 13 other field soils infested with other spp. This is the first report of RPA development for detecting a root-lesion nematode species. The RPA assay developed can help in the rapid detection of this nematode species for effective nematode management.

摘要

据报道,根腐线虫属(Pratylenchus spp.)会在包括大豆在内的多种作物中造成严重的产量损失。2015年在北达科他州(ND)的一个大豆田检测到一种新的根腐线虫物种,并于2021年对其进行了命名。在管理策略中,线虫的检测以及与其他物种的区分至关重要。因此,开发了一种重组酶聚合酶扩增(RPA)检测方法,用于在等温条件下从田间土壤中快速检测这种线虫。根据线虫基因组的内转录间隔区核糖体DNA区域设计了新的引物和探针,并对其特异性和灵敏度进行了测试。使用TwistAmp Basic和Exo试剂盒,RPA检测方法能够在39.5°C下20分钟内从单个成年线虫中检测到DNA。引物的特异性最初通过计算机分析得到确认,随后进行了实验室测试。该检测方法成功扩增了目标物种的DNA,而其他根腐线虫属物种和非目标对照物种均未出现扩增。实时RPA的灵敏度测试表明,它能够从接种无菌土壤中提取的DNA中检测到相当于单个线虫1/32稀释度的DNA。为了进一步验证该检测方法,用在北达科他州采集的19份田间土壤样本进行了测试。通过常规PCR确认的所有受该根腐线虫属侵染的田间样本的土壤DNA提取物,该检测方法均能扩增。它没有扩增来自其他受其他根腐线虫属侵染的13份田间土壤的DNA。这是关于开发用于检测根腐线虫物种的RPA的首次报道。所开发的RPA检测方法有助于快速检测这种线虫物种,以实现有效的线虫管理。