Sensitivity of lateral flow technique for diagnosis of canine parvovirus
- PMID: 38424259
- PMCID: PMC10904390
- DOI: 10.1038/s41598-024-55548-x
Sensitivity of lateral flow technique for diagnosis of canine parvovirus
Abstract
In this study, we devised a nanogold lateral flow immunoassay (LFA-CPV antigen test) for detecting canine parvovirus (CPV) in living attenuated CPV vaccines. We conducted instrumental characterization of the prepared nanogold particles and the developed LFA-CPV antigen test was rigorously evaluated for its performance verification including limit of detection, sensitivity, specificity, selectivity and accuracy. The LFA-CPV antigen test demonstrated strong performance when assessed against qPCR using different batches of live attenuated CPV vaccines, indicated a sensitivity of 96.4%, specificity of 88.2%, and an overall accuracy of 95%. These results suggest that the developed LFA-CPV antigen test could serve as a viable alternative for evaluation live attenuated CPV vaccines, and provide it as a point of care test for CPV diagnosis, offering a potential substitute for traditional laboratory methods, particularly qPCR.
Keywords: Antigen testing; CPV; Canine parvovirus vaccine; Diagnostic testing; Gold nanoparticles; Immuno-chromatographic; Lateral flow assay; Sensitivity and specificity.
© 2024. The Author(s).
Conflict of interest statement
The authors declare no competing interests.
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