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使用具有重组酶聚合酶扩增功能的纳米间隙阻抗传感器通过实时DNA监测进行快速且高灵敏度的病原体检测。

Rapid and highly sensitive pathogen detection by real-time DNA monitoring using a nanogap impedimetric sensor with recombinase polymerase amplification.

作者信息

Lee Hyunjung, Yi So Yeon, Kwon Jung Sun, Choi Jong Min, Lee Dong Su, Lee Sang Hyun, Shin Yong-Beom

机构信息

BioNano Health Guard Research Center (H-GUARD), Daejeon, 34141, Republic of Korea.

BioNano Health Guard Research Center (H-GUARD), Daejeon, 34141, Republic of Korea.

出版信息

Biosens Bioelectron. 2021 May 1;179:113042. doi: 10.1016/j.bios.2021.113042. Epub 2021 Jan 29.

Abstract

Fast detection of pathogens is important for protecting our health and society. Herein, we present a high-performance nanogap impedimetric sensor for monitoring nucleic acid amplification in real time using isothermal recombinase polymerase amplification (RPA) for rapid pathogen detection. The nanogap electrode chip has two pairs of opposing gold electrodes with a 100 nm gap and was fixed to a PCB. Then, the nanogap impedimetric sensor was immersed in RPA reaction solution for the detection of E. coli O157:H7, and target DNA amplification was evaluated through bulk solution impedance changes using impedance spectroscopy every minute during RPA. In addition, target gene amplification in the sample solution during RPA was confirmed with a 2% DNA agarose gel. Our nanogap impedimetric sensor can detect down to a single copy of the eae A gene in gDNA extracted from E. coli O157:H7 as well as a single cell of pathogenic E. coli O157:H7 strain within 5 min during direct RPA, which was performed with the pathogen itself and without the extraction and purification of target gDNA. The miniaturized nanogap impedimetric sensor has potential as a cost-effective point-of-care device for fast and accurate portable pathogen detection via real-time nucleic acid analysis.

摘要

快速检测病原体对于保护我们的健康和社会至关重要。在此,我们展示了一种高性能的纳米间隙阻抗传感器,用于使用等温重组酶聚合酶扩增(RPA)实时监测核酸扩增,以实现快速病原体检测。纳米间隙电极芯片有两对相对的金电极,间隙为100纳米,并固定在印刷电路板上。然后,将纳米间隙阻抗传感器浸入RPA反应溶液中以检测大肠杆菌O157:H7,在RPA过程中每分钟使用阻抗谱通过本体溶液阻抗变化评估目标DNA扩增。此外,用2%的DNA琼脂糖凝胶确认RPA过程中样品溶液中的目标基因扩增。我们的纳米间隙阻抗传感器能够在直接RPA过程中5分钟内检测到从大肠杆菌O157:H7提取的基因组DNA中单个拷贝的eae A基因,以及致病性大肠杆菌O157:H7菌株的单个细胞,该直接RPA是在病原体本身存在的情况下进行的,无需提取和纯化目标基因组DNA。这种小型化的纳米间隙阻抗传感器有潜力成为一种经济高效的即时检测设备,通过实时核酸分析实现快速、准确的便携式病原体检测。

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