重组酶聚合酶扩增
环介导等温扩增
计算生物学
溶解
重组酶
分析物
塔克曼
计算机科学
化学
色谱法
DNA
生物
分子生物学
分析灵敏度
分子信标
灵敏度(控制系统)
聚合酶链反应
样品制备
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
核酸
实时聚合酶链反应
核糖核酸
聚合酶
检出限
聚合酶
作者
Yang-ming Dai,Lei Zhao,Tong Xu,Jia-qi Duan,Yuan-Meng Wang,Yi-Xin Yan,Liang-Peng Ge,Zuo-Hua Liu,Jing Sun,Xiu Zeng,Si-yuan Lai,Yan-Ru Ai,Jianbo Huang,Ling Zhu,Zhi-wen Xu
标识
DOI:10.1021/acssynbio.5c00909
摘要
Rapid and portable diagnostic technologies are essential for controlling infectious diseases. Here, we describe RAPID (Rapid Automated Portable Integrated Detection), a single-step, extraction-free CRISPR-Cas13d-based assay for sensitive and specific detection of porcine deltacoronavirus (PDCoV) RNA. RAPID integrates isothermal recombinase polymerase amplification with EsCas13d-mediated collateral cleavage in a one-pot reaction, enabling sample-to-answer detection within 30 min. A brief room-temperature lysis step allows direct RNA release from unextracted samples, simplifying sample preparation and reducing equipment requirements. Lyophilized reagents enhance stability during refrigerated storage (≤4 °C) and facilitate simplified transportation using conventional cooling measures, thereby reducing reliance on strict cold-chain logistics. The assay operates optimally at 37 °C and remains functional under ambient (∼25 °C) conditions with reduced sensitivity, permitting instrument-free operation when temperature control is unavailable. Detection is achieved via in-tube fluorescence or lateral-flow readouts. Clinical validation using porcine samples showed complete concordance with RT-qPCR, achieving 100% sensitivity and specificity. RAPID provides a practical point-of-care diagnostic platform for on-farm surveillance and deployment in resource-limited settings.
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