Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8478727 | Molecular and Cellular Probes | 2018 | 6 Pages |
Abstract
A visible and equipment-free recombinase polymerase amplification assay combined with a lateral flow strip (LFS RPA) was developed to detect canine parvovirus type 2 (CPV-2), which is the etiological agent of canine parvovirus disease. The CPV-2 LFS RPA assay was developed based on the VP2 gene and is performed in a closed fist using body heat for 15â¯min; the products are visible to the naked eye on the LFS within 5â¯min. The assay could detect CPV-2a, CPV-2b and CPV-2c, and there was no cross-reaction with the other viruses tested. Using the standard CPV-2 DNA as a template, the analytical sensitivity was 1.0â¯Ãâ¯102 copies per reaction, which was the same result as that of a real-time PCR. The assay performance was further evaluated by testing 60 canine fecal samples, and CPV-2 DNA was detected in 46 samples (76.7%, 46/60) by LFS RPA, which was the same result as that of the real-time PCR assay and higher than that of the SNAP method (48.3%, 29/60). The novel CPV-2 LFS RPA assay is an attractive and promising tool for rapid and convenient diagnosis of CPV disease, especially cage side and in underequipped laboratories.
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Authors
Libing Liu, Jianchang Wang, Yunyun Geng, Jinfeng Wang, Ruiwen Li, Ruihan Shi, Wanzhe Yuan,