Rapid, point-of-care molecular diagnostics with Cas13

Shreeya Agrawal(Innovative Genomics Institute), Alison Fanton(University of California, San Francisco), Sita S. Chandrasekaran(University of California, San Francisco), Bérénice Charrez(University of California, San Francisco), Arturo M. Escajeda, Sungmin Son(University of California, Berkeley), Roger McIntosh, Abdul Bhuiya(University of California, San Francisco), María Díaz de León Derby(University of California, San Francisco), Neil A. Switz(San Jose State University), Maxim Armstrong(Lawrence Berkeley National Laboratory), Andrew R. Harris(University of California, Berkeley), Noam Prywes(Innovative Genomics Institute), Maria Lukarska(Innovative Genomics Institute), Scott B. Biering(University of California, Berkeley), Dylan C. J. Smock(Innovative Genomics Institute), Amanda Mok(University of California, Berkeley), Gavin J. Knott(Innovative Genomics Institute), Qi Dang(Innovative Genomics Institute), Erik Van Dis(University of California, Berkeley), Eli Dugan(Innovative Genomics Institute), Shineui Kim(Innovative Genomics Institute), Tina Y. Liu(Innovative Genomics Institute), Eva Harris(University of California, Berkeley), Sarah A. Stanley(University of California, Berkeley), Liana F. Lareau(Innovative Genomics Institute), Ming X. Tan, Daniel A. Fletcher(University of California, Berkeley), Jennifer A. Doudna(Gladstone Institutes), David F. Savage(University of California, Berkeley), Patrick D. Hsu(Innovative Genomics Institute)
medRxiv
December 16, 2020
Cited by 21Open Access
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Abstract

Rapid nucleic acid testing is a critical component of a robust infrastructure for increased disease surveillance. Here, we report a microfluidic platform for point-of-care, CRISPR-based molecular diagnostics. We first developed a nucleic acid test which pairs distinct mechanisms of DNA and RNA amplification optimized for high sensitivity and rapid kinetics, linked to Cas13 detection for specificity. We combined this workflow with an extraction-free sample lysis protocol using shelf-stable reagents that are widely available at low cost, and a multiplexed human gene control for calling negative test results. As a proof-of-concept, we demonstrate sensitivity down to 40 copies/μL of SARS-CoV-2 in unextracted saliva within 35 minutes, and validated the test on total RNA extracted from patient nasal swabs with a range of qPCR Ct values from 13-35. To enable sample-to-answer testing, we integrated this diagnostic reaction with a single-use, gravity-driven microfluidic cartridge followed by real-time fluorescent detection in a compact companion instrument. We envision this approach for Diagnostics with Coronavirus Enzymatic Reporting (DISCoVER) will incentivize frequent, fast, and easy testing.


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