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用于植物病原体现场检测的微针贴片快速提取植物核酸

Rapid Extraction of Plant Nucleic Acids by Microneedle Patch for In-Field Detection of Plant Pathogens.

作者信息

Paul Rajesh, Ostermann Emily, Wei Qingshan

机构信息

Department of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, NC, USA.

Emerging Plant Disease and Global Food Security Cluster, North Carolina State University, Raleigh, NC, USA.

出版信息

Methods Mol Biol. 2022;2536:77-90. doi: 10.1007/978-1-0716-2517-0_4.

Abstract

Plant diseases pose a significant threat to global food security. Molecular diagnosis currently plays a crucial role in mitigating the negative impacts of plant diseases by accurately identifying the disease-causing pathogens and revealing their genotypes. However, current molecular assays are constrained to the laboratory because of the cumbersome protocols involved in plant nucleic acid extraction. To streamline this, we have developed a polymeric microneedle (MN) patch-based nucleic acid extraction method, which can be applied to various plant tissues and easily performed in field settings without using bulky laboratory equipment. The MN patch instantly isolates both host and pathogen's DNA and RNA from plant leaves by two simple steps: press and rinse with a buffer solution or nuclease-free water. The MN-extracted DNA and RNA are purification-free and directly applicable to downstream molecular assays such as polymerase chain reaction (PCR), reverse transcription-polymerase chain reaction (RT-PCR), loop-mediated isothermal amplification (LAMP), and reverse transcription loop-mediated isothermal amplification (RT-LAMP). Here, we describe the fabrication procedures of the MN patch and demonstrate the application of the MN method by extracting Phytophthora infestans DNA and tomato spotted wilt virus (TSWV) RNA from infected tomato leaves. After MN extraction, we directly utilize the MN-extracted nucleic acid samples to run PCR, RT-PCR, LAMP, or RT-LAMP reactions to amplify various biomarker genes, such as the ribulose-bisphosphate carboxylase (rbcL) gene of host tomato DNA, internal transcribed spacer (ITS) region of P. infestans DNA, and nucleocapsid (N) gene of TSWV RNA. Furthermore, this simple and rapid nucleic acid method can be integrated with portable nucleic acid amplification platforms such as smartphone-based microscopy devices to achieve "sample-to-answer" detection of plant pathogens directly in the field.

摘要

植物病害对全球粮食安全构成重大威胁。目前,分子诊断通过准确识别致病病原体并揭示其基因型,在减轻植物病害的负面影响方面发挥着关键作用。然而,由于植物核酸提取过程繁琐,目前的分子检测仅限于实验室。为了简化这一过程,我们开发了一种基于聚合物微针(MN)贴片的核酸提取方法,该方法可应用于各种植物组织,并且无需使用大型实验室设备即可在野外轻松进行。MN贴片通过两个简单步骤即可立即从植物叶片中分离出宿主和病原体的DNA和RNA:按压并用缓冲溶液或无核酸酶水冲洗。MN提取的DNA和RNA无需纯化,可直接用于下游分子检测,如聚合酶链反应(PCR)、逆转录-聚合酶链反应(RT-PCR)、环介导等温扩增(LAMP)和逆转录环介导等温扩增(RT-LAMP)。在这里,我们描述了MN贴片的制备过程,并通过从受感染的番茄叶片中提取致病疫霉DNA和番茄斑萎病毒(TSWV)RNA,展示了MN方法的应用。MN提取后,我们直接利用MN提取的核酸样本进行PCR、RT-PCR、LAMP或RT-LAMP反应,以扩增各种生物标志物基因,如宿主番茄DNA的核酮糖-1,5-二磷酸羧化酶(rbcL)基因、致病疫霉DNA的内转录间隔区(ITS)区域以及TSWV RNA的核衣壳(N)基因。此外,这种简单快速的核酸方法可以与便携式核酸扩增平台(如基于智能手机的显微镜设备)集成,以直接在野外实现植物病原体的“样本到答案”检测。

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