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Development of Enzyme-Mediated Duplex Exponential Amplification Assay for Detection and Identification of Meloidogyne enterolobii in Field

文献类型： 外文期刊

作者： Sun, Bingxue 1 ; Gao, Bo 1 ; Wang, Rongyan 1 ; Chen, Shulong 1 ; Li, Xiuhua 1 ; Dong, Yonghao 1 ; Ma, Juan 1 ;

作者机构： 1.Minist Agr & Rural Affairs, Int Sci & Technol Joint Res Ctr IPM Hebei Prov, IPM Innovat Ctr Hebei Prov, Key Lab Integrated Pest Management Crops Northern, Baoding 071030, Peoples R China; Hebei Acad Agr & Forestry Sci, Plant Protect Inst, Baoding 071030, Peoples R China

关键词： Meloidogyne enterolobii; detection; isothermal amplification

期刊名称：MICROORGANISMS （ 影响因子：4.2； 五年影响因子：4.6 ）

ISSN：

年卷期： 2025 年 13 卷 6 期

页码：

收录情况： SCI

摘要： The root-knot nematode Meloidogyne enterolobii has emerged as a devastating pathogen in global agricultural systems. Its geographic distribution is progressively expanding from tropical to temperate zones, leading to difficulties in discerning the symptoms it causes from those of congeners such as M. incognita. Currently, some molecular diagnostic technologies (e.g., qPCR) have been established for detecting M. enterolobii, but these methods fail to meet field-based detection demands due to their reliance on laboratory-grade thermocyclers. We thus developed a method for detecting M. enterolobii based on enzyme-mediated duplex exponential amplification (EmDEA) technologies to address this issue. The EmDEA detection method demonstrated strict specificity for the target species, showing no amplification in 13 non-target nematodes or host tissue samples. Sensitivity analyses revealed detection limits of 3.6 x 10(-4) ng/mu L (purified DNA), 1/1000 of an individual nematode (single-organism detection), 8.97 nematodes/g sweet potato, and 4.08 nematodes/100 g soil, achieving equivalent performance to qPCR. Field validation confirmed successful on-site detection, with significantly higher nematode loads in root tissues (50.41-97.62 nematodes/g) than in rhizospheric soil (1.07-1.28 nematodes/g). The established detection method employs a 42 degrees C isothermal amplification technology paired with a palm-sized thermal module, enabling field-deployable detection. Its unique duplex exponential amplification mechanism achieves threshold determination 10 cycles (similar to 10 min) faster than conventional qPCR. When integrated with rapid DNA extraction protocols, the entire workflow is completed within 40 min, improving detection efficiency. This study provides a molecular tool for the precise monitoring of M. enterolobii, offering critical support for formulating targeted control strategies.

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