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Recombinase-aided amplification coupled with lateral flow dipstick for efficient and accurate detection of Bombyx mori nucleopolyhedrovirus
R. Wang, S. Xu, E. Wei, P. He, Y. Zhang, Q. Wang, X. Tang, Z. Shen
Status minimal Language English Country Czech Republic
Document type Journal Article, Evaluation Study
- MeSH
- Bombyx * virology MeSH
- DNA, Viral genetics MeSH
- Limit of Detection MeSH
- Nucleopolyhedroviruses * genetics isolation & purification MeSH
- Recombinases * metabolism genetics MeSH
- Sensitivity and Specificity MeSH
- Nucleic Acid Amplification Techniques * methods MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
- Publication type
- Journal Article MeSH
- Evaluation Study MeSH
The infection of Bombyx mori nucleopolyhedrovirus (BmNPV) is one of the main causes of economic losses in sericulture. Thus, it is essential to establish rapid and effective method for BmNPV detection. In the present study, we have developed a recombinase-aided amplification (RAA) to amplify the BmNPV genomic DNA at 37 °C within 30 min, and achieved a rapid detection method by coupling with a lateral flow dipstick (LFD). The RAA-LFD method had a satisfactory detection limit of 6 copies/μL of recombinant plasmid pMD19-T-IE1, and BmNPV infection of silkworm can be detected 12 h post-infection. This method was highly specific for BmNPV, and without cross-reactivity to other silkworm pathogens. In contrast to conventional polymerase chain reaction (PCR), the RAA-LFD assay showed higher sensitivity, cost-saving, and especially is apt to on-site detection of BmNPV infection in the sericulture production.
Institute of Sericulture Chinese Academy of Agricultural Sciences Zhenjiang China
School of Biotechnology Jiangsu University of Science and Technology Zhenjiang China
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