Rapid Detection of Genotype II African Swine Fever Virus Using CRISPR Cas13a-Based Lateral Flow Strip

Bibliographic Details
Title: Rapid Detection of Genotype II African Swine Fever Virus Using CRISPR Cas13a-Based Lateral Flow Strip
Authors: Ning Wei, Bohan Zheng, Junjun Niu, Tao Chen, Jing Ye, Youhui Si, Shengbo Cao
Source: Viruses, Vol 14, Iss 2, p 179 (2022)
Publisher Information: MDPI AG, 2022.
Publication Year: 2022
Collection: LCC:Microbiology
Subject Terms: CRISPR/Cas13a, RAA, lateral flow strip, African swine fever, detection, Microbiology, QR1-502
More Details: The African swine fever virus (ASFV) is a dsDNA virus that can cause serious, highly infectious, and fatal diseases in wild boars and domestic pigs. The ASFV has brought enormous economic loss to many countries, and no effective vaccine or treatment for the ASFV is currently available. Therefore, the on-site rapid and accurate detection of the ASFV is key to the timely implementation of control. The RNA-guided, RNA-targeting CRISPR effector CRISPR-associated 13 (Cas13a; previously known as C2c2) exhibits a “collateral effect” of promiscuous RNase activity upon the target recognition. The collateral cleavage activity of LwCas13a is activated to degrade the non-targeted RNA, when the crRNA of LwCas13a binds to the target RNA. In this study, we developed a rapid and sensitive ASFV detection method based on the collateral cleavage activity of LwCas13a, which combines recombinase-aided amplification (RAA) and a lateral flow strip (named CRISPR/Cas13a-LFD). The method was an isothermal detection at 37 °C, and the detection can be used for visual readout. The detection limit of the CRISPR/Cas13a-LFD was 101 copies/µL of p72 gene per reaction, and the detection process can be completed within an hour. The assay showed no cross-reactivity to eight other swine viruses, including classical swine fever virus (CSFV), and has a 100% coincidence rate with real-time PCR detection of the ASFV in 83 clinical samples. Overall, this method is sensitive, specific, and practicable onsite for the ASFV detection, showing a great application potential for monitoring the ASFV in the field.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1999-4915
Relation: https://www.mdpi.com/1999-4915/14/2/179; https://doaj.org/toc/1999-4915
DOI: 10.3390/v14020179
Access URL: https://doaj.org/article/38c319fef2bd4721beb2ac456c0a7714
Accession Number: edsdoj.38c319fef2bd4721beb2ac456c0a7714
Database: Directory of Open Access Journals
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More Details
ISSN:19994915
DOI:10.3390/v14020179
Published in:Viruses
Language:English