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A Smartphone-Read Ultrasensitive and Quantitative Saliva Test for COVID-19
abstract
This abstract is available on the publisher's site.
Access this abstract nowImproved point-of-care COVID-19 assays are urgently needed to improve disease control efforts, but current assays lack the sensitivity of the RT-PCR gold-standard. Herein we describe the development of a portable, ultrasensitive saliva-based COVID-19 assay with a 15 minute sample-to-answer time that does not require RNA isolation or laboratory equipment. This assay uses CRISPR/Cas12a activity to enhance signal from an amplified viral RNA target, which is stimulated by laser diode integrated into a smartphone-based fluorescence microscope readout device. This device robustly quantified viral load over a broad linear range (1-105 copies/μL) and exhibited a limit of detection (0.38 copies/μL) below that of the RT-PCR reference assay. SARS-CoV-2 RNA levels read by CRISPR were similar in patient saliva versus nasal swab samples and viral loads measured by RT-PCR and the smartphone-read CRISPR assay demonstrated good correlation, supporting the potential utility of this portable assay device for saliva-based point-of-care COVID-19 diagnosis.
Additional Info
A Smartphone-Read Ultrasensitive and Quantitative Saliva Test for COVID-19
Sci Adv 2021 Jan 08;7(2)eabe3703, B Ning, T Yu, S Zhang, Z Huang, D Tian, Z Lin, A Niu, N Golden, K Hensley, B Threeton, CJ Lyon, XM Yin, CJ Roy, NS Saba, J Rappaport, Q Wei, TY HuFrom MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.