| Literature DB >> 33310733 |
Bo Ning1,2, Tao Yu3, Shengwei Zhang3, Zhen Huang1,2,4, Di Tian5, Zhen Lin5, Alex Niu6, Nadia Golden7,8, Krystle Hensley8, Breanna Threeton7, Christopher J Lyon1,2, Xiao-Ming Yin5, Chad J Roy9, Nakhle S Saba6, Jay Rappaport7,8,9, Qingshan Wei3, Tony Y Hu1,2.
Abstract
Improved 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.Entities:
Year: 2020 PMID: 33310733 DOI: 10.1126/sciadv.abe3703
Source DB: PubMed Journal: Sci Adv ISSN: 2375-2548 Impact factor: 14.136