Department of Plant Pathology, University of Agricultural Sciences, Bangalore, India.
Rice Pathology Laboratory, All India Coordinated Rice Improvement Programme, University of Agricultural Sciences, Raichur, India.
Sci Rep. 2021 Jan 8;11(1):178. doi: 10.1038/s41598-020-80644-z.
Rice blast (caused by Magnaporthe oryzae) and sheath rot diseases (caused by Sarocladium oryzae) are the most predominant seed-borne pathogens of rice. The detection of both pathogens in rice seed is essential to avoid production losses. In the present study, a microdevice platform was designed, which works on the principles of loop-mediated isothermal amplification (LAMP) to detect M. oryzae and S. oryzae in rice seeds. Initially, a LAMP, polymerase chain reaction (PCR), quantitative PCR (qPCR), and helicase dependent amplification (HDA) assays were developed with primers, specifically targeting M. oryzae and S. oryzae genome. The LAMP assay was highly efficient and could detect the presence of M. oryzae and S. oryzae genome at a concentration down to 100 fg within 20 min at 60 °C. Further, the sensitivity of the LAMP, HDA, PCR, and qPCR assays were compared wherein; the LAMP assay was highly sensitive up to 100 fg of template DNA. Using the optimized LAMP assay conditions, a portable foldable microdevice platform was developed to detect M. oryzae and S. oryzae in rice seeds. The foldable microdevice assay was similar to that of conventional LAMP assay with respect to its sensitivity (up to 100 fg), rapidity (30 min), and specificity. This platform could serve as a prototype for developing on-field diagnostic kits to be used at the point of care centers for the rapid diagnosis of M. oryzae and S. oryzae in rice seeds. This is the first study to report a LAMP-based foldable microdevice platform to detect any plant pathogens.
稻瘟病(由稻瘟病菌引起)和纹枯病(由立枯丝核菌引起)是水稻最主要的种传病原菌。在水稻种子中检测这两种病原菌对于避免生产损失至关重要。在本研究中,设计了一种微器件平台,该平台基于环介导等温扩增(LAMP)的原理,用于检测水稻种子中的稻瘟病菌和立枯丝核菌。最初,我们使用针对稻瘟病菌和立枯丝核菌基因组的引物,开发了 LAMP、聚合酶链反应(PCR)、定量 PCR(qPCR)和解旋酶依赖扩增(HDA)检测方法。LAMP 检测法非常高效,在 60°C 下 20 分钟内可检测到低至 100 fg 的稻瘟病菌和立枯丝核菌基因组的存在。此外,我们比较了 LAMP、HDA、PCR 和 qPCR 检测方法的灵敏度,结果表明 LAMP 检测法对模板 DNA 的灵敏度高达 100 fg。在优化 LAMP 检测条件的基础上,我们开发了一种可折叠的便携式微器件平台,用于检测水稻种子中的稻瘟病菌和立枯丝核菌。该可折叠微器件检测法在灵敏度(高达 100 fg)、快速性(30 分钟)和特异性方面与传统 LAMP 检测法相似。该平台可作为开发现场诊断试剂盒的原型,用于在护理点中心快速诊断水稻种子中的稻瘟病菌和立枯丝核菌。这是第一项报道基于 LAMP 的可折叠微器件平台用于检测任何植物病原菌的研究。