4.8 Article

An ultrasensitive and rapid sample-to-answer microsystem for on-site monitoring of SARS-CoV-2 in aerosols using in situ tetra-primer recombinase polymerase amplification

Journal

BIOSENSORS & BIOELECTRONICS
Volume 219, Issue -, Pages -

Publisher

ELSEVIER ADVANCED TECHNOLOGY
DOI: 10.1016/j.bios.2022.114816

Keywords

Aerosol; SARS-CoV-2; COVID-19; Filter paper; Recombinase polymerase amplification; Microfluidics

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The airborne transmissibility of SARS-CoV-2 has created an urgent need for aerosol monitoring to prevent sporadic outbreaks of COVID-19. We have developed a novel monitoring system that combines high sensitivity and a short turnaround time. By testing clinical samples, we have demonstrated the excellent performance of our system and its potential application in fighting the COVID-19 pandemic.
Airborne transmissibility of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has highlighted the urgent need for aerosol monitoring of SARS-CoV-2 to prevent sporadic outbreaks of COVID-19. The inadequate sensitivity of conventional methods and the lack of an on-site detection system limited the practical SARS-CoV-2 monitoring of aerosols in public spaces. We have developed a novel SARS-CoV-2-in-aerosol monitoring system (SIAMs) which consists of multiple portable cyclone samplers for collecting aerosols from several venues and a sensitive sample-to-answer microsystem employing an integrated cartridge for the analysis of SARS-CoV-2 in aerosols (iCASA) near the sampling site. By seamlessly combining viral RNA extraction based on a chitosan-modified quartz filter and in situ tetra-primer recombinase polymerase amplification (tpRPA) into an inte-grated microfluidic cartridge, iCASA can provide an ultra-high sensitivity of 20 copies/mL, which is nearly one order of magnitude greater than that of the commercial kit, and a short turnaround time of 25 min. By testing various clinical samples of nasopharyngeal swabs, saliva, and exhaled breath condensates obtained from 23 COVID-19 patients, we demonstrate that the positive rate of our system was 3.3 times higher than those of the conventional method. Combining with multiple portable cyclone samplers, we detected 52.2% (12/23) of the aerosol samples, six times higher than that of the commercial kit, collected from the isolation wards of COVID-19 patients, demonstrating the excellent performance of our system for SARS-CoV-2-in-aerosol monitoring. We envision the broad application of our microsystem in aerosol monitoring for fighting the COVID-19 pandemic.

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