Application of CRISPR-Cas12a Enhanced Fluorescence Assay Coupled with Nucleic Acid Amplification for the Sensitive Detection of African Swine Fever Virus

• Published in: ACS synthetic biology Vol. 9; no. 9; pp. 2339 - 2350
• Main Authors: Tao, Dagang, Liu, Jiajia, Nie, Xiongwei, Xu, Bingrong, Tran-Thi, Thuy-Nhien, Niu, Lili, Liu, Xiangdong, Ruan, Jinxue, Lan, Xiaochen, Peng, Guiqing, Sun, Limeng, Ma, Yunlong, Li, Xinyun, Li, Congcong, Zhao, Shuhong, Xie, Shengsong
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 18-09-2020
• Subjects: African Swine Fever Virus - genetics; African Swine Fever Virus - isolation & purification; Animals; CRISPR-Cas Systems - genetics; DNA - chemistry; DNA, Viral - analysis; DNA, Viral - metabolism; Fluorescent Dyes - chemistry; Limit of Detection; Nucleic Acid Amplification Techniques - methods; RNA, Guide, CRISPR-Cas Systems - genetics; RNA, Guide, CRISPR-Cas Systems - metabolism; Swine - genetics; Swine - virology; nucleic acid detection; African swine fever virus; CRISPR-Cas12a enhanced fluorescence assay; pig
• ISSN: 2161-5063; 2161-5063
• DOI: 10.1021/acssynbio.0c00057

African swine fever (ASF) is one of the most severe diseases of pigs. In this study, a CRISPR-Cas12a (also known as Cpf1) system coupled with nucleic acid amplification was optimized for the detection of ASF virus (ASFV). Two novel single-stranded DNA-fluorophore-quencher (ssDNA-FQ) reporters were developed to increase the brightness of the fluorescent signal for the visualization of nucleic acid detection. The CRISPR-Cas12a system was used to simultaneously cleave the polymerase chain reaction (PCR) or loop-mediated isothermal amplification (LAMP) amplicons and the newly developed ssDNA-FQ reporter, resulting in fluorescence that could be easily detected in multiple platforms, especially on cheap and portable blue or UV light transilluminators. This specific cleavage with fluorescence reveals the presence of the amplicon and confirms its identity, thereby preventing false-positive test results from nonspecific amplicons. This method is also uninterfered by the presence of large amounts of irrelevant background DNA and displays no cross-reactivity with other porcine DNA or RNA viruses. When coupled with LAMP, the Cas12a platform can detect a plasmid containing p72 with as few as 2 copies/μL reaction. Our results indicate that the CRISPR-Cas12a enhanced fluorescence assay coupled with nucleic acid amplification is robust, convenient, specific, confirmatory, affordable, and potentially adaptable for ASF diagnosis.