Rapid Visual Detection of African Swine Fever Virus with a CRISPR/Cas12a Lateral Flow Strip Based on Structural Protein Gene D117L

非洲猪瘟病毒 病毒学 病毒 生物 聚合酶链反应 基因 非洲猪瘟 重组DNA DNA 分子生物学 遗传学
作者
Desheng Zhang,Sen Jiang,Nengwen Xia,Youwen Zhang,Jiajia Zhang,Anjing Liu,Chenyang Zhang,Nanhua Chen,François Meurens,Wanglong Zheng,Jianzhong Zhu
出处
期刊:Animals [MDPI AG]
卷期号:13 (23): 3712-3712 被引量:5
标识
DOI:10.3390/ani13233712
摘要

African swine fever virus (ASFV) is a large double-stranded DNA virus that is highly infectious and seriously affects domestic pigs and wild boars. African swine fever (ASF) has caused huge economic losses to endemic countries and regions. At present, there is still a lack of effective vaccines and therapeutics. Therefore, rapid and accurate detection is essential for the prevention and control of ASF. The portable DNA endonuclease (Cas12a)-mediated lateral flow strip detection method (Cas12a-LFS) combined with recombinant polymerase amplification (RPA) has been gradually recognized as effective for virus detection including ASFV. In this study, based on the ASFV structural protein p17 gene (D117L), an RPA-Cas12a-LFS detection method was established. The detection method exhibits a sensitivity of up to two gene copies and has no cross-reaction with nine other swine viruses. Thus, the method is highly sensitive and specific. In 68 clinical samples, the coincidence rate of the p17 strip was 100%, compared to the traditional quantitative PCR (qPCR). In conclusion, we have developed a simple, rapid, sensitive, and specific ASFV visual detection method and demonstrated the potential of on-site detection of ASFV.

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