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基于CRISPR-Cas12b系统的伪狂犬病病毒超灵敏可视化检测

Ultrasensitive and visual detection of pseudorabies virus based on CRISPR-Cas12b system.

作者信息

Kang Haoran, Yang Xintan, Jiang Ruijiao, Gao Peng, Zhang Yongning, Zhou Lei, Ge Xinna, Han Jun, Guo Xin, Yang Hanchun

机构信息

State Key Laboratory of Veterinary Public Health and Safety, Key Laboratory of Animal Epidemiology of the Ministry of Agriculture and Rural Affairs, College of Veterinary Medicine, China Agricultural University, Beijing, People's Republic of China.

State Key Laboratory of Veterinary Public Health and Safety, Key Laboratory of Animal Epidemiology of the Ministry of Agriculture and Rural Affairs, College of Veterinary Medicine, China Agricultural University, Beijing, People's Republic of China.

出版信息

Microb Pathog. 2025 Jun;203:107447. doi: 10.1016/j.micpath.2025.107447. Epub 2025 Mar 1.

Abstract

Aujeszky's disease (AD) is an acute infectious disease that infects pigs and other animals, resulting in significant economic losses and posing a threat to human health. Reliable and rapid detection methods are essential for the prevention of AD. In this study, a RAA-Cas12b assay based on recombinase-aided amplification (RAA) and CRISPR-Cas12b system was established, optimized and evaluated for the rapid detection of wild-type Pseudorabies Virus (PRV). The results can not only be detected by real-time fluorescence readout, but also can be visualized by a portable blue light instrument. There was no cross-reaction with PRV Bartha-K61 strain or other swine infectious viruses. The analytical sensitivities of the real-time PRV RAA-Cas12b assay and visual PRV RAA-Cas12b assay were determined to be 15 copies/μL with 95 % confidence interval and 140 copies/μL with 95 % confidence interval, respectively. A total of 31 clinical samples were detected and compared with PRV qPCR assay to evaluate the diagnostic performance of the PRV RAA-Cas12b assay. The diagnostic coincidence rate of the two assays was 100 %. In summary, this convenient and reliable assay has great potential for rapid detection of wild type PRV in point-of-care testing (POCT).

摘要

奥耶斯基氏病(AD)是一种感染猪和其他动物的急性传染病,会导致重大经济损失,并对人类健康构成威胁。可靠且快速的检测方法对于预防AD至关重要。在本研究中,建立、优化并评估了一种基于重组酶辅助扩增(RAA)和CRISPR-Cas12b系统的RAA-Cas12b检测方法,用于快速检测野生型伪狂犬病病毒(PRV)。结果不仅可以通过实时荧光读数进行检测,还可以通过便携式蓝光仪器进行可视化。与PRV巴塔-K61株或其他猪传染性病毒无交叉反应。实时PRV RAA-Cas12b检测方法和可视化PRV RAA-Cas12b检测方法的分析灵敏度分别确定为95%置信区间下的15拷贝/μL和95%置信区间下的140拷贝/μL。共检测了31份临床样本,并与PRV qPCR检测方法进行比较,以评估PRV RAA-Cas12b检测方法的诊断性能。两种检测方法的诊断符合率为100%。总之,这种便捷可靠的检测方法在即时检测(POCT)中快速检测野生型PRV具有巨大潜力。

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