Development of a Real-Time Quantitative RT-PCR Assay for Detection of Bovine Rhinitis B Virus

被引:6
|
作者
Xie, Yi-Lun [1 ,2 ]
Lv, Dian-Hong [2 ]
Wen, Xiao-Hui [2 ]
Zhai, Qi [2 ]
Luo, Man-Lin [1 ]
Wei, Wen-Kang [2 ,3 ]
Chen, Qin-Ling [2 ,3 ]
Zhai, Shao-Lun [2 ]
机构
[1] South China Agr Univ, Coll Vet Med, Guangzhou, Peoples R China
[2] Guangdong Acad Agr Sci, Inst Anim Hlth, Key Lab Anim Dis Prevent Guangdong Prov,Minist Ag, Sci Observat & Expt Stn Vet Drugs & Diagnost Tech, Guangzhou, Peoples R China
[3] Guangdong Acad Agr Sci, Agrobiol Gene Res Ctr, Guangzhou, Peoples R China
关键词
bovine rhinitis B virus; RT-qPCR; TaqMan probe; detection; assay; DISEASE; CALF;
D O I
10.3389/fvets.2021.680707
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Bovine rhinitis B virus (BRBV) has been frequently identified in cattle diagnosed with bovine respiratory disease complex (BRDC) in recent years, suggesting its potential contribution to BRDC. The goal of this study was to develop a TaqMan-based real-time quantitative RT-PCR assay for efficient BRBV detection. A pair of primers and a probe were designed based on the 3D gene of the BRBV genome. The assay was specific for BRBV and able to exclude bovine rhinitis A virus, foot-and-mouth disease virus and Senecavirus A. The limit of detection of the assay was 4.46 copies per reaction. A standard curve was plotted, with a coefficient of determination of 0.999 in the concentration range of 10(0)-10(8) copies/mu l. The reproducibility of the assay was acceptable, with the standard deviations of cycle threshold values lower than 1.00 in both intra- and inter-assay. Of 200 samples collected from 150 head of cattle in recent years in China, 11% (22/200) of the samples tested positive in the assay, i.e., 4.6% (7/150) of the cattle were BRBV positive. This study provides an efficient diagnostic tool for the epidemiological investigations of BRBV.
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页数:6
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