Literature DB >> 33662816

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

Hyunjung Lee1, So Yeon Yi2, Jung Sun Kwon2, Jong Min Choi2, Dong Su Lee3, Sang Hyun Lee4, Yong-Beom Shin5.   

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.
Copyright © 2021 Elsevier B.V. All rights reserved.

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Keywords:  Nanogap impedimetric sensor; Pathogen detection; Point-of-care test (POCT); Real-time; Recombinase polymerase amplification (RPA)

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Year:  2021        PMID: 33662816     DOI: 10.1016/j.bios.2021.113042

Source DB:  PubMed          Journal:  Biosens Bioelectron        ISSN: 0956-5663            Impact factor:   10.618


  1 in total

1.  Biosensing bacterial 16S rDNA by microchip electrophoresis combined with a CRISPR system based on real-time crRNA/Cas12a formation.

Authors:  Feifei Luo; Xing Geng; Zhi Li; Ge Dai; Zhaohui Chu; Pingang He; Fan Zhang; Qingjiang Wang
Journal:  RSC Adv       Date:  2022-08-10       Impact factor: 4.036

  1 in total

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