Zhang Pian, Ren Zhaowen, Gao Xiaopeng, Zhao Mengpo, Wang Yanyun, Chen Jing, Wang Gang, Xiang Hua, Cai Rujian, Luo Shengjun, Wang Xiaohu
Key Laboratory of Livestock Disease Prevention of Guangdong Province, Key Laboratory for Prevention and Control of Avian Influenza and Other Major Poultry Diseases, Ministry of Agriculture and Rural Affairs, Guangdong Provincial Observation and Research Station for Animal Disease, Institute of Animal Health, Guangdong Academy of Agricultural Sciences, Guangzhou, China.
College of Veterinary Medicine, South China Agricultural University, Guangzhou, China.
Front Vet Sci. 2024 Apr 26;11:1353439. doi: 10.3389/fvets.2024.1353439. eCollection 2024.
Porcine circoviruses disease (PCVD), caused by porcine circovirus (PCVs), is an important swine disease characterized by porcine dermatitis, nephrotic syndrome and reproductive disorders in sows. However, diseases caused by PCV2, PCV3, or PCV4 are difficult to distinguish, so a simple, rapid, accurate and high-throughput diagnostic and identification method is urgently needed to differentiate these three types. In this study, specific primers and probes were designed based on the conserved region sequences of the Rep gene of PCV2, and the Cap gene of PCV3 and PCV4. A multiplex qPCR assay was developed and optimized that the limit of detection concentration could reach as low as 3.8 copies/μL, with all correlation coefficients (R) exceeding 0.999. Furthermore, the method showed no cross-reaction with other crucial porcine viral pathogens, and both intra-repeatability and inter-reproducibility coefficients of variation were below 2%. The assay was applied to the detection of 738 pig samples collected from 2020 to 2021 in Guangdong Province, China. This revealed positive infection rates of 65.18% for PCV2, 29.27% for PCV3, and 0% for PCV4, with a PCV2/PCV3 co-infection rate of 23.17%. Subsequently, complete genome sequences of 17 PCV2 and 4 PCV3 strains were obtained from the above positive samples and pre-preserved positive circovirus samples. Nucleotide sequence analysis revealed that the 17 PCV2 strains shared 96.7-100% complete nucleotide identity, with 6 strains being PCV2b and 11 strains being PCV2d; the 4 PCV3 strains shared 98.9-99.4% complete nucleotide identity, with 2 strains being PCV3a-1 and 2 strains being PCV3b. This research provides a reliable tool for rapid PCVs identification and detection. Molecular epidemiological investigation of PCVs in pigs in Guangdong Province will help us to understand PCV2 and PCV3 epidemiological characteristics and evolutionary trends.
猪圆环病毒病(PCVD)由猪圆环病毒(PCVs)引起,是一种重要的猪病,其特征为猪皮炎、肾病综合征以及母猪繁殖障碍。然而,由PCV2、PCV3或PCV4引起的疾病难以区分,因此迫切需要一种简单、快速、准确且高通量的诊断和鉴定方法来区分这三种类型。在本研究中,基于PCV2的Rep基因、PCV3和PCV4的Cap基因的保守区域序列设计了特异性引物和探针。开发并优化了一种多重qPCR检测方法,其检测限浓度可低至3.8拷贝/μL,所有相关系数(R)均超过0.999。此外,该方法与其他重要的猪病毒病原体无交叉反应,重复内和重复间变异系数均低于2%。该检测方法应用于对2020年至2021年在中国广东省采集的738份猪样本的检测。结果显示,PCV2的阳性感染率为65.18%,PCV3为29.27%,PCV4为0%,PCV2/PCV3共感染率为23.17%。随后,从上述阳性样本和预先保存的阳性圆环病毒样本中获得了17株PCV2和4株PCV3毒株的完整基因组序列。核苷酸序列分析表明,17株PCV2毒株的完整核苷酸同一性为96.7 - 100%,其中6株为PCV2b,11株为PCV2d;4株PCV3毒株的完整核苷酸同一性为98.9 - 99.4%,其中2株为PCV3a - 1,2株为PCV3b。本研究为快速鉴定和检测PCVs提供了可靠工具。对广东省猪群中PCVs的分子流行病学调查将有助于我们了解PCV2和PCV3的流行病学特征及进化趋势。