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1.The Experimental Teaching Center, College of Animal Sciences, Zhejiang University, Hangzhou 310058, China
2.MOA Key Laboratory of Animal Virology, Zhejiang University Center for Veterinary Sciences, Hangzhou 310058, China
收稿:2025-11-13,
修回:2026-02-24,
网络首发:2026-08-13,
纸质出版:2026-08-13
金玉兰,季暄,董伟仁等.基于gN基因的伪狂犬病病毒TaqMan qPCR分型方法的建立及应用[J].浙江大学学报(英文版)(B辑:生物医学和生物技术),2026,27(08):923-926.
Yulan JIN, Xuan JI, Weiren DONG, et al. Development and application of a novel TaqMan qPCR assay targeting the
金玉兰,季暄,董伟仁等.基于gN基因的伪狂犬病病毒TaqMan qPCR分型方法的建立及应用[J].浙江大学学报(英文版)(B辑:生物医学和生物技术),2026,27(08):923-926. DOI: 10.1631/jzus.B2500729.
Yulan JIN, Xuan JI, Weiren DONG, et al. Development and application of a novel TaqMan qPCR assay targeting the
伪狂犬病是由伪狂犬病病毒(PRV)引起的一种严重危害全球养猪业的传染病,由于不同基因型毒株的致病性与流行特征存在差异,临床上需建立一种能够快速、准确区分PRV基因I型和基因II型的分型检测方法。本研究首次以
gN
基因为靶标,基于其保守区域鉴别稳定差异序列,成功建立了一种TaqMan三重实时荧光定量聚合酶链式反应(PCR)检测方法。该方法不仅可检测PRV感染,而且能有效区分其基因型。该检测方法具有特异性强、灵敏度高、重复性好及操作简便等优点。该检测体系仅需一对引物和三个探针即可完成分型鉴定,极大简化了反应体系,降低了引物错配及非特异性扩增的风险。对实验动物来源样本初步应用的结果显示,该方法能准确检测PRV的感染情况及其基因型。本研究为PRV的分子流行病学监测提供了实用、高效的技术工具,也为猪群中PRV的净化工作提供了有力支持。
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