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集成微针-智能手机核酸扩增平台,用于现场诊断植物病害。

Integrated microneedle-smartphone nucleic acid amplification platform for in-field diagnosis of plant diseases.

机构信息

Department of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, NC, 27696, USA.

Department of Entomology and Plant Pathology, North Carolina State University, Raleigh, NC, 27695, USA.

出版信息

Biosens Bioelectron. 2021 Sep 1;187:113312. doi: 10.1016/j.bios.2021.113312. Epub 2021 May 8.

DOI:10.1016/j.bios.2021.113312
PMID:34004545
Abstract

We demonstrate an integrated microneedle (MN)-smartphone nucleic acid amplification platform for "sample-to-answer" diagnosis of multiplexed plant pathogens within 30 min. This portable system consists of a polymeric MN patch for rapid nucleic acid extraction within a minute and a 3D-printed smartphone imaging device for loop-mediated isothermal amplification (LAMP) reaction and detection. We expanded the extraction of the MN technology for DNA targets as in the previous study (ACS Nano, 2019, 13, 6540-6549) to more fragile RNA biomarkers, evaluated the storability of the extracted nucleic acid samples on MN surfaces, and developed a smartphone-based LAMP amplification and fluorescent reader device that can quantify four LAMP reactions on the same chip. In addition, we have found that the MN patch containing as few as a single needle tip successfully extracted enough RNA for RT-PCR or RT-LAMP analysis. Moreover, MN-extracted RNA samples remained stable on MN surfaces for up to three days. The MN-smartphone platform has been used to detect both Phytophthora infestans DNA and tomato spotted wilt virus (TSWV) RNA down to 1 pg, comparable to the results from a benchtop thermal cycler. Finally, multiplexed detection of P. infestans and TSWV through a single extraction from infected tomato leaves and amplification on the smartphone without benchtop equipment was demonstrated.

摘要

我们展示了一种集成的微针(MN)-智能手机核酸扩增平台,用于在 30 分钟内对多种植物病原体进行“从样本到答案”的诊断。这个便携式系统由一个聚合物 MN 贴片组成,用于在一分钟内快速提取核酸,以及一个 3D 打印的智能手机成像设备,用于环介导等温扩增(LAMP)反应和检测。我们将 MN 技术的提取扩展到了以前研究中的 DNA 靶标(ACS Nano,2019,13,6540-6549),以提取更脆弱的 RNA 生物标志物,评估了提取的核酸样本在 MN 表面的存储稳定性,并开发了一种基于智能手机的 LAMP 扩增和荧光读取设备,能够在同一芯片上定量四个 LAMP 反应。此外,我们发现,即使只有一个针尖的 MN 贴片也能成功提取足够的 RNA 进行 RT-PCR 或 RT-LAMP 分析。此外,MN 提取的 RNA 样本在 MN 表面上的稳定性长达三天。MN-智能手机平台已用于检测马铃薯晚疫病菌 DNA 和番茄斑萎病毒(TSWV)RNA,灵敏度低至 1 pg,与台式热循环仪的结果相当。最后,通过从感染的番茄叶片中进行单次提取和在智能手机上进行扩增,无需台式设备,实现了对 P. infestans 和 TSWV 的多重检测。

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