4.7 Review

Development and application of sensitive, specific, and rapid CRISPR-Cas13-based diagnosis

Journal

JOURNAL OF MEDICAL VIROLOGY
Volume 93, Issue 7, Pages 4198-4204

Publisher

WILEY
DOI: 10.1002/jmv.26889

Keywords

clustered regularly interspaced short palindromic repeats (CRISPR)‐ associated genes 13; coronavirus disease 2019; nucleic acid detection; severe acute respiratory syndrome coronavirus‐ 2; specific high‐ sensitivity enzymatic reporter unlocking

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CRISPR-Cas13 diagnostic assays have high sensitivity and specificity, with rapid, inexpensive, and portable detection (<2 h, $0.05 per test). Based on Cas13 guided by crRNA, this system's collateral cleavage activity allows for detection of target sequences in sample RNA. The recent development of micro-well chips facilitates high-level multiplexing and is high-throughput.
Nucleic acid detection is a necessary part of medical treatment and fieldwork. However, the current detection technologies are far from ideal. A lack of timely and accessible testing for identifying cases and close contacts has allowed severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), the causative virus of the ongoing coronavirus disease-2019 (COVID-19) pandemic, to spread uncontrollably. The slow and expensive detection of mutations-predictors for chronic diseases such as cancer-form a barrier to personalized treatment. A recently developed diagnostic assay is ideal and field-ready-it relies on CRISPR-Cas13. CRISPR-Cas13 works similarly to other CRISPR systems: Cas13 is guided by a crRNA to cleave next to a specific RNA target sequence. Additionally, Cas13 boasts a unique collateral cleavage activity; collateral cleavage of a fluorescent reporter detects the presence of the target sequence in sample RNA. This system forms the basis of CRISPR-Cas13 diagnostic assays. CRISPR-Cas13 assays have >95% sensitivity and >99% specificity. Detection is rapid (<2 h), inexpensive ($0.05 per test), and portable-a test using lateral flow strips is akin to a pregnancy test. The recent adaptation of micro-well chips facilitates high-level multiplexing and is high-throughput. In this review, we cover the development of CRISPR-Cas13 assays for medical diagnosis, discuss the advantages of CRISPR-Cas13-based diagnosis over the traditional reverse transcription polymerase chain reaction (RT-PCR), and present examples of detection from real patient samples.

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