Development of a TaqMan probe-based dual real time PCR assay for the identification of NADC34-like PRRSV

IF 1.9 Q2 AGRICULTURE, DAIRY & ANIMAL SCIENCE
Shanshan Han , Tao Qin , Taichun Chen , Xiaocheng Xing , Qiang Zhang
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Abstract

Porcine reproductive and respiratory syndrome virus (PRRSV) is an RNA virus that induces reproductive disorders in sows and respiratory diseases in growing pigs. Recently, the NADC34-like strain of PRRSV has become more prevalent, with outbreaks occurring across pig farms in China. However, a reliable diagnostic method for the clinical detection of this strain has been absent. This study developed a TaqMan probe-based dual real-time quantitative PCR assay targeting the M and GP5 genes to specifically identify the NADC34-like PRRSV strain. The assay exhibited high specificity, detecting exclusively the NADC34-like strain without cross-reactivity with other PRRSV strains. The detection limits for pMD-M and pMD-GP5 plasmids were 2.67 × 10² and 1.35 × 10¹ copies/μL, respectively, indicating high assay sensitivity. The assay also demonstrated excellent reproducibility, with coefficient of variation (CV) values for both recombinant plasmids below 2 %. Among 251 clinical samples, 27 tested positive for NADC34-like PRRSV. This study establishes an accurate, sensitive, and reliable TaqMan dual real-time PCR assay for detecting NADC34-like PRRSV, offering a valuable tool for clinical diagnostics and outbreak management in pig farms.
基于TaqMan探针的双实时PCR方法鉴定nadc34样PRRSV的建立
猪繁殖与呼吸综合征病毒(PRRSV)是一种RNA病毒,可引起母猪繁殖障碍和生长猪呼吸道疾病。最近,nadc34样PRRSV毒株变得更加普遍,在中国的养猪场发生了疫情。然而,临床检测该菌株的可靠诊断方法一直缺乏。本研究建立了一种基于TaqMan探针的双实时定量PCR检测方法,针对M和GP5基因特异性鉴定nadc34样PRRSV菌株。该方法特异性高,只检测到nadc34样菌株,与其他PRRSV株无交叉反应性。pMD-M和pMD-GP5质粒的检出限分别为2.67 × 10²和1.35 × 10¹拷贝/μL,具有较高的灵敏度。该试验还显示了良好的再现性,两种重组质粒的变异系数(CV)值均低于2%。251份临床样本中,27份检测出nadc34样PRRSV阳性。本研究建立了一种准确、灵敏、可靠的TaqMan双实时PCR检测nadc34样PRRSV的方法,为猪场的临床诊断和疫情管理提供了有价值的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Veterinary and Animal Science
Veterinary and Animal Science Veterinary-Veterinary (all)
CiteScore
3.50
自引率
0.00%
发文量
43
审稿时长
47 days
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