Development and Application of a Multiplex Real-Time TaqMan qPCR Assay for the Simultaneous Detection of African Swine Fever Virus, Classical Swine Fever Virus, Porcine Reproductive and Respiratory Syndrome Virus, Pseudorabies Virus, and Porcine Circovirus Type 2

伪狂犬病 猪繁殖与呼吸综合征病毒 非洲猪瘟病毒 猪圆环病毒 猪瘟 病毒学 生物 病毒 塔克曼 猪细小病毒 多路复用 动脉瘤 实时聚合酶链反应 多重聚合酶链反应 聚合酶链反应 基因 医学 遗传学 病理 疾病 传染病(医学专业) 2019年冠状病毒病(COVID-19)
作者
Dongdong Yin,Shuangshuang Xu,Yayun Liu,Hao Guo,M.D. Lan,Lei Yin,Jieru Wang,Yin Dai,Xuehuai Shen,Kai Zhan,Xiaocheng Pan
出处
期刊:Microorganisms [Multidisciplinary Digital Publishing Institute]
卷期号:13 (7): 1573-1573
标识
DOI:10.3390/microorganisms13071573
摘要

Since its emergence in China in 2018, African swine fever virus (ASFV) has posed a severe threat to the pig farming industry due to its high transmissibility and mortality rate. The clinical signs of ASFV infection often overlap with those caused by other swine viruses such as classical swine fever virus (CSFV), porcine reproductive and respiratory syndrome virus (PRRSV), pseudorabies virus (PRV), and porcine circovirus type 2 (PCV2), making timely and precise diagnosis a considerable challenge. To address this, we established a TaqMan-based multiplex real-time quantitative PCR (qPCR) assay capable of simultaneously detecting ASFV, CSFV, PRRSV, PRV, and PCV2. Specific primer-probe sets were developed targeting conserved genomic regions: the ASFV P72 gene, CSFV 5’UTR region, PRRSV ORF6, PCV2 cap gene, and PRV gB gene. After thorough optimization, the assay demonstrated robust analytical performance, exhibiting strong target specificity with no cross-detection of non-target pathogens. The detection threshold was determined to be 10 copies/μL per virus, indicating high assay sensitivity. Repeatability analysis revealed low variability, with intra- and inter-assay coefficient of variation values remaining below 2.3%. When applied to 95 clinical samples, the multiplex assay yielded results that were fully consistent with those obtained using commercially available singleplex qPCR kits. In conclusion, the multiplex TaqMan qPCR method developed in this study is characterized by high specificity, sensitivity, and reproducibility. It provides a reliable and efficient diagnostic tool for the simultaneous detection and differential diagnosis of ASFV and other clinically similar viral infections in swine, thereby offering robust technical support for swine disease surveillance and control.
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