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DNA Virus Detection System Based on RPA-CRISPR/Cas12a-SPM and Deep Learning
Published on: May 10, 2024
Detection of duck adenovirus 3 using RAA-CRISPR/Cas12a based lateral flow dipstick method
Wenyu Zhang1,2, Zhiwang Tang1,2, Siwen He1,2
1School of Life Sciences, Fujian Agriculture and Forestry University, Fuzhou, China.
Abstract:
Duck adenovirus 3 (DAdV-3) was firstly identified in Muscovy ducklings exhibiting slight pericardial effusion, swelling, and hemorrhaging in the kidneys, which is a poorly characterized duck virus. This study established a CRISPR/Cas12a coupled with a Lateral flow dipstick (RAA-CRISPR/Cas12a-LFD) detection platform for DAdV-3. The core mechanism of this platform involves a three-step cascade reaction pathway. First, the target sequence of the DAdV-3100 k gene is amplified via RAA isothermal amplification. Second, the amplified products activate the trans-cleavage activity of Cas12a. Finally, signal output is achieved by cleaving probes on the Lateral flow dipstick. This method exhibits high sensitivity, with a minimum detection limit of 2.87 × 102 copies/μL for the DAdV-3 positive plasmid. It also demonstrates high specificity for DAdV-3, showing no cross-reactivity with other common duck-origin viruses such as avian influenza virus (AIV), Newcastle disease virus (NDV), duck Tembusu virus (DTMUV), duck plague virus (DPV), Muscovy duck parvovirus (MDPV), duck hepatitis A virus type 1 (DHAV-1), and duck reovirus (DRV). The method enables on-site detection of DAdV-3 within 1 h and 20 min. It does not rely on standardized molecular laboratories or professional operation, provides visualized detection results, allows rapid detection at the grassroots level, and has low detection costs, making it suitable for promotion in small-scale farms. This approach provides a technical means for the detection and epidemiological investigation of DAdV-3.
Insights
A new rapid detection platform for Duck adenovirus 3 (DAdV-3) was developed using CRISPR/Cas12a and a lateral flow dipstick. This sensitive and specific method allows for quick, on-site DAdV-3 diagnosis, aiding in disease control in duck farms.
Area of Science:
- Veterinary Virology
- Molecular Diagnostics
- Biosensing Technology
Background:
- Duck adenovirus 3 (DAdV-3) is an emerging pathogen causing significant morbidity in Muscovy ducklings.
- Current diagnostic methods for DAdV-3 are often time-consuming and require specialized laboratory equipment.
- There is a critical need for rapid, sensitive, and field-deployable diagnostic tools for DAdV-3.
Purpose of the Study:
- To establish a novel, rapid, and sensitive detection platform for Duck adenovirus 3 (DAdV-3).
- To develop a CRISPR/Cas12a-based assay coupled with a Lateral Flow Dipstick (LFD) for visual DAdV-3 detection.
- To evaluate the sensitivity, specificity, and practical applicability of the developed diagnostic platform.
Main Methods:
- Utilized Recombinase Aided Amplification (RAA) for isothermal amplification of DAdV-3 target genes.
- Employed CRISPR-Cas12a system to leverage its trans-cleavage activity on amplified products.
- Integrated the CRISPR-Cas12a system with a Lateral Flow Dipstick (LFD) for visual signal readout.
Main Results:
- The RAA-CRISPR/Cas12a-LFD platform achieved a low detection limit of 2.87 × 10^2 copies/μL for DAdV-3 plasmid.
- Demonstrated high specificity, with no cross-reactivity against common duck viruses like AIV, NDV, DTMUV, DPV, MDPV, DHAV-1, and DRV.
- Enabled visual detection of DAdV-3 within 1 hour and 20 minutes, suitable for on-site applications.
Conclusions:
- The developed RAA-CRISPR/Cas12a-LFD assay is a sensitive, specific, and rapid method for DAdV-3 detection.
- This platform offers a cost-effective and user-friendly alternative for on-site diagnostics, particularly beneficial for small-scale duck farms.
- The assay provides a valuable tool for DAdV-3 epidemiological surveillance and disease management in the poultry industry.
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