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

被引:12
|
作者
Cao, Nan [1 ]
Tang, Zhihui [2 ]
Zhang, Xiyu [2 ]
Li, Wanyan [1 ]
Li, Bingxin [1 ]
Tian, Yunbo [1 ]
Xu, Danning [1 ]
机构
[1] Zhongkai Univ Agr & Engn, Coll Anim Sci & Technol, Guangdong Prov Key Lab Waterfowl Hlth Breeding, Guangzhou, Peoples R China
[2] Nanjing Agr Univ, Coll Vet Med, MOE Joint Int Res Lab Anim Hlth & Food Safety, Nanjing, Peoples R China
基金
中国博士后科学基金;
关键词
triplex qRT-PCR; FCV; FPV; FHV-1; clinical detection; CHLAMYDOPHILA-FELIS; RESPIRATORY-TRACT; MUCOSAL SWABS; CATS; MULTIPLEX; MICROBIOLOGY; VALIDATION; INFECTION; SYSTEMS; VIRUS;
D O I
10.3389/fvets.2021.792322
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
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.
引用
收藏
页数:10
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