化学
清脆的
病毒学
重组酶聚合酶扩增
DNA
非洲猪瘟病毒
检出限
病毒
分子生物学
色谱法
基因
环介导等温扩增
生物化学
生物
作者
Dan Zhu,Tong Su,Tao Sun,Xingcai Qin,Shao Su,Yun Bai,Fang Li,Dongming Zhao,Guoqing Shao,Jie Chao,Zhixin Feng,Lianhui Wang
标识
DOI:10.1021/acs.analchem.3c05364
摘要
Accurate, ultrasensitive, and point-of-care (POC) diagnosis of the African swine fever virus (ASFV) remains imperative to prevent its spread and limit the losses incurred. Herein, we propose a CRISPR-Cas12a-assisted triplex amplified colorimetric assay for ASFV DNA detection with ultrahigh sensitivity and specificity. The specific recognition of recombinase aided amplification (RAA)-amplified ASFV DNA could activate the Cas12a/crRNA/ASFV DNA complex, leading to the digestion of the linker DNA (bio-L1) on magnetic beads (MBs), thereby preventing its binding of gold nanoparticles (AuNPs) network. After magnetic separation, the release of AuNPs network comprising a substantial quantity of AuNPs could lead to a discernible alteration in color and significantly amplify the plasmonic signal, which could be read by spectrophotometers or smartphones. By combining the RAA, CRISPR/Cas12a-assisted cleavage, and AuNPs network-mediated colorimetric amplification together, the assay could detect as low as 0.1 copies/μL ASFV DNA within 1 h. The assay showed an accuracy of 100% for the detection of ASFV DNA in 16 swine tissue fluid samples, demonstrating its potential for on-site diagnosis of ASFV.
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