| Literature DB >> 29665412 |
Chunhe Wan1, Longfei Cheng2, Guanghua Fu2, Cuiteng Chen2, Rongchang Liu2, Shaohua Shi2, Hongmei Chen2, Qiuling Fu2, Yu Huang3.
Abstract
Due to low doses of infection, an efficient and sensitive virus detection method is necessary to detect low amounts of goose hemorrhagic polyomavirus (GHPV). In this study, we have developed a TaqMan real-time PCR (qPCR) specific assay for the detection of GHPV. Specificity assay showed no cross-reactions with other common waterfowl viruses. The standard curve had a linear correlation of 0.997 and efficiency of 99% between the cycle threshold value and the logarithm of the plasmids copy number. The possible lowest detectable concentration was 35.4 copies/μl; 100 times more sensitive than conventional PCR (detection limit, 3.54 × 103 copies/μl). Domestic Jinyun Sheldrakes ducks and their embryonated eggs were found positive of GHPV infection which provides evidence of possible vertical transmission of GHPV.Entities:
Keywords: Domestic Jinyun Sheldrakes; Goose hemorrhagic polyomavirus; Sensitivity; TaqMan real-time PCR
Mesh:
Year: 2018 PMID: 29665412 DOI: 10.1016/j.mcp.2018.04.003
Source DB: PubMed Journal: Mol Cell Probes ISSN: 0890-8508 Impact factor: 2.365