Zhang Yongzhe, Wang Meiqi, Sun Yajuan, Xiao Xingyu, Wang Songsong, Li Peng, Liu Yansong, Zhao Hongri, Meng Yan, Yin Rui
College of Biological and Pharmaceutical Engineering, Jilin Agricultural Science and Technology University, Jilin 132101, China.
Department of Neurology, China-Japan Union Hospital of Jilin University, Changchun 130033, China.
Vet Sci. 2024 Jun 28;11(7):289. doi: 10.3390/vetsci11070289.
To establish a rapid real-time RT-PCR method for differentiating wild-type classical swine fever virus (CSFV) strains from vaccine strains (HCLV), we designed a universal primer targeting the gene to detect wild-type CSFV strains and vaccine strains simultaneously, and two TaqMan-MGB probes were designed to differentiate between wild-type and vaccine strains. After optimizing the RT-qPCR conditions, a rapid dual TaqMan-MGB RT-qPCR method for the detection and identification of CSFV and HCLV was developed. The results showed that method could specifically detect CSFV and HCLV with no cross-reactivity with other swine pathogens. The analytic sensitivity for the gene of CSFV and HCLV were 1.67 × 10 copies/μL, respectively. For precision testing, the repeatability and reproducibility of the test was less than 2%. This method was successfully used for the rapid detection of 193 biological samples collected from CSFV-vaccinated pigs. This fast and accurate detection technology can be used for the detection of CSFV and is suitable for differentiating between wild-type CSFV strains and vaccine strains.
为建立一种快速实时RT-PCR方法以区分野生型经典猪瘟病毒(CSFV)毒株和疫苗株(HCLV),我们设计了一对靶向 基因的通用引物,用于同时检测野生型CSFV毒株和疫苗株,并设计了两条TaqMan-MGB探针以区分野生型和疫苗株。优化RT-qPCR条件后,建立了一种用于检测和鉴定CSFV及HCLV的快速双TaqMan-MGB RT-qPCR方法。结果表明,该方法能特异性检测CSFV和HCLV,与其他猪病原体无交叉反应。CSFV和HCLV的 基因分析灵敏度分别为1.67×10拷贝/μL。在精密度测试中,该检测的重复性和再现性均小于2%。该方法成功用于对193份来自接种CSFV疫苗猪的生物样品的快速检测。这种快速准确的检测技术可用于CSFV的检测,适用于区分野生型CSFV毒株和疫苗株。