Zhengzhou Key Laboratory for Pig Disease Prevention and Control, College of Veterinary Medicine, Henan Agricultural University, Zhengdong New District Longzi Lake 15#, Zhengzhou, 450046, Henan Province, People's Republic of China.
Zhengzhou Key Laboratory for Pig Disease Prevention and Control, College of Veterinary Medicine, Henan Agricultural University, Zhengdong New District Longzi Lake 15#, Zhengzhou, 450046, Henan Province, People's Republic of China.
J Virol Methods. 2021 Jul;293:114152. doi: 10.1016/j.jviromet.2021.114152. Epub 2021 Apr 15.
Porcine circovirus 4 (PCV4) was a novel circovirus identified from diseased pigs in 2019 in Hunan Province, China, and PCV3 and PCV4 co-infection has been reported. In order to detect and differentiate PCV3 and PCV4 simultaneously, the SYBR Green І-based duplex quantitative PCR (qPCR) assay was established in the present study. The two viruses could be easily distinguished by different Tm values: 86.5°C for PCV3 and 79°C for PCV4, while other porcine pathogens did not shown specific melting peaks. The detection limits of this duplex qPCR assay were 51.7 copies/μL for PCV3 and 67.7 copies/μL for PCV4, and both of the intra-assay and inter-assay of the CV analysis of this assay were less than 2.0 %. Sixty-four clinical samples from 22 different swine farms were screened by the duplex qPCR assay. The results showed that the positive detection rate of PCV3 was 37.5 % (24/64) and PCV4 was 34.38 % (22/64), and PCV3 and PCV4 co-infection rate was 17.19 % (11/64). The detection rate of the duplex qPCR assay was higher than that of the conventional PCR assay. The duplex qPCR was of high sensitivity and specificity, being able to provide technical support for clinical detection, differential diagnosis and control of PCV3 and PCV4.
猪圆环病毒 4 型(PCV4)是 2019 年在中国湖南省从患病猪中鉴定出的一种新型圆环病毒,已有报道称 PCV3 和 PCV4 同时感染。为了同时检测和区分 PCV3 和 PCV4,本研究建立了基于 SYBR Green І 的双重实时定量 PCR(qPCR)检测方法。两种病毒可以通过不同的 Tm 值(PCV3 为 86.5°C,PCV4 为 79°C)轻松区分,而其他猪病原体则没有特异性的熔解峰。该双重 qPCR 检测方法的检测限为 PCV3 为 51.7 拷贝/μL,PCV4 为 67.7 拷贝/μL,该方法的 CV 分析的内和间试验重复性均小于 2.0%。用双重 qPCR 检测方法对来自 22 个不同猪场的 64 份临床样本进行了筛查。结果显示,PCV3 的阳性检出率为 37.5%(24/64),PCV4 为 34.38%(22/64),PCV3 和 PCV4 混合感染率为 17.19%(11/64)。双重 qPCR 检测方法的检出率高于常规 PCR 检测方法。双重 qPCR 具有较高的灵敏度和特异性,能够为 PCV3 和 PCV4 的临床检测、鉴别诊断和防控提供技术支持。