Fast and Simplified CRISPR–Cas13d Assay for Sensitive Detection of Porcine Deltacoronavirus

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Authors: 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
+3 more Jianbo Huang, Ling Zhu, Zhiwen Xu
Cited by: 0
References: 42

Abstract

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.

Fields of Study & Subjects

Biosensors and Analytical Detection SARS-CoV-2 detection and testing CRISPR and Genetic Engineering

Publication details

Journal / source
ACS Synthetic Biology
Volume
15
Issue
2
Pages
834–845
Publication date
11 February 2026
Language
EN