4.7 Article

Development and Application of a Triplex TaqMan Quantitative Real-Time PCR Assay for Simultaneous Detection of Feline Calicivirus, Feline Parvovirus, and Feline Herpesvirus 1

Journal

FRONTIERS IN VETERINARY SCIENCE
Volume 8, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fvets.2021.792322

Keywords

triplex qRT-PCR; FCV; FPV; FHV-1; clinical detection

Funding

  1. Jiangsu Agriculture Science and Technology Innovation Fund (JASTIF) [CX[21]3174]
  2. Forestry Science and Technology Innovation and Promotion Project of Jiangsu Province [LYKJ[2018]22, LYKJ[2021]40]
  3. Fundamental Research Funds for the Central Universities [KJQN202136]
  4. Fellowship of China Postdoctoral Science Foundation [2020M681650]
  5. Priority Academic Program Development of Jiangsu Higher Education Institutions

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Felines are crucial companions in human families, and the detection and intervention of common viruses like FCV, FHV-1, and FPV are essential for preventing severe infectious diseases in baby cats. A triplex TaqMan qRT-PCR assay with high sensitivity, excellent repeatability, and good specificity was developed in this study, showing higher accuracy compared to commercial kits for clinical diagnosis.
As companion animals, felines play an important role in human's family life, and their healthcare has attracted great attention. Viruses such as feline calicivirus (FCV), feline herpesvirus 1 (FHV-1), and feline parvovirus virus (FPV) are the most common pathogens that cause severe infectious disease in baby cats. Thus, preclinical detection and intervention of these three viruses is an effective means to prevent diseases and minimize their danger condition. In this study, a triplex TaqMan quantitative real-time polymerase chain reaction (qRT-PCR) assay was developed to detect these three viruses simultaneously. The detection limit of FPV, FCV, and FHV-1 was 5 x 10(1) copies/assay, which exhibited higher sensitivity (about 10- to100-fold) than conventional PCR. The coefficients of variation (CVs) of the intra-assay variability were lower than 1.86%, and that of inter-assay variability were lower than 3.19%, indicating the excellent repeatability and reproducibility of the triplex assay. Additionally, the assay showed good specificity. Finally, samples from 48 cats were analyzed using the established assay and commercial kits. As a result, the total positive rates for these viruses were 70.83 or 62.5%, respectively, which demonstrated that the developed qRT-PCR assay was more accurate than the commercial kits and could be used in clinical diagnosis.

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