Rapid electrochemical detection of coronavirus SARS-CoV-2

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作者
Thanyarat Chaibun
Jiratchaya Puenpa
Tatchanun Ngamdee
Nimaradee Boonapatcharoen
Pornpat Athamanolap
Anthony Peter O’Mullane
Sompong Vongpunsawad
Yong Poovorawan
Su Yin Lee
Benchaporn Lertanantawong
机构
[1] Mahidol University,Biosensors Laboratory, Department of Biomedical Engineering, Faculty of Engineering
[2] Chulalongkorn University,Center of Excellence in Clinical Virology, Faculty of Medicine
[3] King Mongkut’s University of Technology Thonburi,Department of Biotechnology, School of Bioresources and Technology
[4] King Mongkut’s University of Technology Thonburi,Pilot Plant Development and Training Institute (PDTI)
[5] Queensland University of Technology (QUT),School of Chemistry and Physics
[6] AIMST University,Faculty of Applied Sciences
[7] AIMST University,Centre of Excellence for Omics
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摘要
Coronavirus disease 2019 (COVID-19) is a highly contagious disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Diagnosis of COVID-19 depends on quantitative reverse transcription PCR (qRT-PCR), which is time-consuming and requires expensive instrumentation. Here, we report an ultrasensitive electrochemical biosensor based on isothermal rolling circle amplification (RCA) for rapid detection of SARS-CoV-2. The assay involves the hybridization of the RCA amplicons with probes that were functionalized with redox active labels that are detectable by an electrochemical biosensor. The one-step sandwich hybridization assay could detect as low as 1 copy/μL of N and S genes, in less than 2 h. Sensor evaluation with 106 clinical samples, including 41 SARS-CoV-2 positive and 9 samples positive for other respiratory viruses, gave a 100% concordance result with qRT-PCR, with complete correlation between the biosensor current signals and quantitation cycle (Cq) values. In summary, this biosensor could be used as an on-site, real-time diagnostic test for COVID-19.
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