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使用Cas13的快速即时分子诊断

Rapid, point-of-care molecular diagnostics with Cas13.

作者信息

Agrawal Shreeya, Fanton Alison, Chandrasekaran Sita S, Charrez Bérénice, Escajeda Arturo M, Son Sungmin, Mcintosh Roger, Bhuiya Abdul, de León Derby María Díaz, Switz Neil A, Armstrong Maxim, Harris Andrew R, Prywes Noam, Lukarska Maria, Biering Scott B, Smock Dylan C J, Mok Amanda, Knott Gavin J, Dang Qi, Van Dis Erik, Dugan Eli, Kim Shin, Liu Tina Y, Harris Eva, Stanley Sarah A, Lareau Liana F, Tan Ming X, Fletcher Daniel A, Doudna Jennifer A, Savage David F, Hsu Patrick D

机构信息

Department of Bioengineering, University of California, Berkeley, Berkeley, CA, USA.

Innovative Genomics Institute, University of California, Berkeley, Berkeley, CA, USA.

出版信息

medRxiv. 2021 Apr 5:2020.12.14.20247874. doi: 10.1101/2020.12.14.20247874.

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.

摘要

快速核酸检测是加强疾病监测强大基础设施的关键组成部分。在此,我们报告了一种用于即时护理的基于CRISPR的分子诊断微流控平台。我们首先开发了一种核酸检测方法,该方法将针对高灵敏度和快速动力学优化的DNA和RNA扩增的不同机制相结合,并与用于特异性检测的Cas13检测相联系。我们将此工作流程与使用易于保存且广泛可得的低成本试剂的免提取样品裂解方案以及用于判定阴性检测结果的多重人类基因对照相结合。作为概念验证,我们展示了在35分钟内对未提取唾液中低至40拷贝/μL的SARS-CoV-2的检测灵敏度,并使用一系列qPCR Ct值为13 - 35的患者鼻拭子提取的总RNA对该检测进行了验证。为实现从样本到答案的检测,我们将这种诊断反应与一次性重力驱动微流控盒集成,并在紧凑型配套仪器中进行实时荧光检测。我们设想这种冠状病毒酶促报告诊断方法(DISCoVER)将促进频繁、快速且简便的检测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7b2/8030690/e643d8b2f14b/nihpp-2020.12.14.20247874-f0001.jpg

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