» Articles » PMID: 38293281

Multiplex Solid-phase RPA Coupled CRISPR-based Visual Detection of SARS-CoV-2

Overview
Specialty Biotechnology
Date 2024 Jan 31
PMID 38293281
Authors
Affiliations
Soon will be listed here.
Abstract

The COVID-19 pandemic has presented a significant challenge to the world's public health and led to over 6.9 million deaths reported to date. A rapid, sensitive, and cost-effective point-of-care virus detection device is essential for the control and surveillance of the contagious severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) pandemic. The study presented here aimed to demonstrate a solid-phase isothermal recombinase polymerase amplification coupled CRISPR-based (spRPA-CRISPR) assay for on-chip multiplexed, sensitive and visual COVID-19 DNA detection. The assay targets the SARS-CoV-2 structure protein encoded genomes and can simultaneously detect two specific genes without cross-interaction. The amplified target sequences were immobilized on the one-pot device surface and detected using the mixed Cas12a-crRNA collateral cleavage of reporter-released fluorescent signal when specific genes were recognized. The endpoint signal can be directly visualized for rapid detection of COVID-19. The system was tested with samples of a broad range of concentrations (20 to 2 × 10 copies) and showed analytical sensitivity down to 20 copies per microliter. Furthermore, a low-cost blue LED flashlight (~$12) was used to provide a visible SARS-CoV-2 detection signal of the spRPA-CRISPR assay which could be purchased online easily. Thus, our platform provides a sensitive and easy-to-read multiplexed gene detection method that can specifically identify low concentration genes.

Citing Articles

Nanoplasmonic microarray-based solid-phase amplification for highly sensitive and multiplexed molecular diagnostics: application for detecting SARS-CoV-2.

Lee J, Jang H, Kim S, Kang T, Park S, Lee M Mikrochim Acta. 2024; 191(11):715.

PMID: 39472332 PMC: 11522150. DOI: 10.1007/s00604-024-06723-4.


Current Trends in RNA Virus Detection via Nucleic Acid Isothermal Amplification-Based Platforms.

Ngoc L, Lee Y Biosensors (Basel). 2024; 14(2).

PMID: 38392016 PMC: 10886876. DOI: 10.3390/bios14020097.

References
1.
Ruff P, Donnianni R, Glancy E, Oh J, Symington L . RPA Stabilization of Single-Stranded DNA Is Critical for Break-Induced Replication. Cell Rep. 2016; 17(12):3359-3368. PMC: 5218512. DOI: 10.1016/j.celrep.2016.12.003. View

2.
Ramachandran A, Huyke D, Sharma E, Sahoo M, Huang C, Banaei N . Electric field-driven microfluidics for rapid CRISPR-based diagnostics and its application to detection of SARS-CoV-2. Proc Natl Acad Sci U S A. 2020; 117(47):29518-29525. PMC: 7703567. DOI: 10.1073/pnas.2010254117. View

3.
Iwamoto T, Sonobe T, Hayashi K . Loop-mediated isothermal amplification for direct detection of Mycobacterium tuberculosis complex, M. avium, and M. intracellulare in sputum samples. J Clin Microbiol. 2003; 41(6):2616-22. PMC: 156570. DOI: 10.1128/JCM.41.6.2616-2622.2003. View

4.
Poon L, Zandberg W, Hsiao D, Erno Z, Sen D, Gates B . Photothermal release of single-stranded DNA from the surface of gold nanoparticles through controlled denaturating and Au-S bond breaking. ACS Nano. 2010; 4(11):6395-403. DOI: 10.1021/nn1016346. View

5.
Lee S, Kim Y, Yeo W . Advances in Microsensors and Wearable Bioelectronics for Digital Stethoscopes in Health Monitoring and Disease Diagnosis. Adv Healthc Mater. 2021; 10(22):e2101400. DOI: 10.1002/adhm.202101400. View