A multiplexed Cas13-based assay with point-of-care attributes for simultaneous COVID-19 diagnosis and variant surveillance
Author:
Patchsung MaturadaORCID, Homchan AimornORCID, Aphicho KanokpolORCID, Suraritdechachai SurasedORCID, Wanitchanon ThanyapatORCID, Pattama Archiraya, Sappakhaw Khomkrit, Meesawat Piyachat, Wongsatit ThanakritORCID, Athipanyasilp Artittaya, Jantarug Krittapas, Athipanyasilp Niracha, Buahom Juthamas, Visanpattanasin SupapatORCID, Niljianskul NootareeORCID, Chaiyen PimchaiORCID, Tinikul Ruchanok, Wichukchinda NuanjunORCID, Mahasirimongkol SurakamethORCID, Sirijatuphat RujipasORCID, Angkasekwinai NasikarnORCID, Crone Michael A.ORCID, Freemont Paul S.ORCID, Joung JuliaORCID, Ladha Alim, Abudayyeh Omar, Gootenberg JonathanORCID, Zhang Feng, Chewapreecha ClaireORCID, Chanarat SittinanORCID, Horthongkham NavinORCID, Pakotiprapha DanayaORCID, Uttamapinant ChayasithORCID
Abstract
AbstractPoint-of-care (POC) nucleic acid detection technologies are poised to aid gold-standard technologies in controlling the COVID-19 pandemic, yet shortcomings in the capability to perform critically needed complex detection—such as multiplexed detection for viral variant surveillance—may limit their widespread adoption. Herein, we developed a robust multiplexed CRISPR-based detection using LwaCas13a and PsmCas13b to simultaneously diagnose SARS-CoV-2 infection and pinpoint the causative SARS-CoV-2 variant of concern (VOC)— including globally dominant VOCs Delta (B.1.617.2) and Omicron (B.1.1.529)—all while maintaining high levels of accuracy upon the detection of multiple SARS-CoV-2 gene targets. The platform has several attributes suitable for POC use: premixed, freeze-dried reagents for easy use and storage; convenient direct-to-eye or smartphone-based readouts; and a one-pot variant of the multiplexed detection. To reduce reliance on proprietary reagents and enable sustainable use of such a technology in low- and middle-income countries, we locally produced and formulated our own recombinase polymerase amplification reaction and demonstrated its equivalent efficiency to commercial counterparts. Our tool—CRISPR-based detection for simultaneous COVID-19 diagnosis and variant surveillance which can be locally manufactured—may enable sustainable use of CRISPR diagnostics technologies for COVID- 19 and other diseases in POC settings.
Publisher
Cold Spring Harbor Laboratory
Reference55 articles.
1. Nextclade: clade assignment, mutation calling and quality control for viral genomes;Journal of Open Source Software,2021 2. SARS-CoV-2 genomic and subgenomic RNAs in diagnostic samples are not an indicator of active replication;Nature Communications,2020 3. Arizti-Sanz, J. , Bradley, A. D. , Zhang, Y. B. , Boehm, C. K. , Freije, C. A. , Grunberg, M. E. , Kosoko-Thoroddsen, T.-S. F. , Welch, N. L. , Pillai, P. P. , Mantena, S. , Kim, G. , Uwanibe, J. N. , John, O. G. , Eromon, P. E. , Kocher, G. , Gross, R. , Lee, J. S. , Hensley, L. E. , Happi, C. T. , … Myhrvold, C. (2021). Equipment-free detection of SARS-CoV-2 and Variants of Concern using Cas13. medRxiv, 2021.2011.2001.21265764. https://doi.org/10.1101/2021.11.01.21265764 4. Streamlined inactivation, amplification, and Cas13-based detection of SARS-CoV-2;Nature Communications,2020 5. Quenching of Unincorporated Amplification Signal Reporters in Reverse-Transcription Loop-Mediated Isothermal Amplification Enabling Bright, Single-Step, Closed-Tube, and Multiplexed Detection of RNA Viruses
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