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A novel SERS-based lateral flow assay for differential diagnosis of wild-type pseudorabies virus and gE-deleted vaccine

机译:一种基于SERS的新型侧向流分析方法,用于鉴别野生型伪狂犬病病毒和缺失gE的疫苗

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摘要

Pseudorabies virus (PRV) is a pathogen that causes an acute infectious disease in pigs, which could lead to huge losses to the farming industry. The Bartha-K61 strain of PRV, commonly used as a gE-deleted vaccine, does not always protect against the wild-type virus infection effectively. Therefore, the prompt detection of viral infection in gE-deleted vaccine vaccinated pigs is crucial for in-time measures to prevent the spread of diseases. In this study, we developed a Surface-enhanced Raman spectroscopy(SERS) based lateral flow assay based on antigen-antibody reaction to meet the demand. Our method was rapid (15 min), sensitive (LOD: 5 ng mL(-1)), selective for wild-type PRV detection, and quantitatively or semi-quantitatively (DLR: 41-650 ng mL(-1)) compatible. The detection results from this method were consistent with results from the gE-specific PCR, indicating that this SERS-based lateral flow assay could be used as a new tool to differentially diagnose wild-type PRV and gE-deleted vaccine.
机译:伪狂犬病病毒(PRV)是一种病原体,可引起猪的急性传染病,并可能给养殖业造成巨大损失。 PRV的Bartha-K61株通常被用作gE缺失疫苗,但并不总是能有效地防止野生型病毒感染。因此,及时检出已接种gE疫苗的猪中的病毒感染对于及时预防疾病传播至关重要。在这项研究中,我们开发了基于抗原-抗体反应的基于表面增强拉曼光谱(SERS)的侧向流动测定法,以满足需求。我们的方法快速(15分钟),灵敏(LOD:5 ng mL(-1)),对野生型PRV检测具有选择性,并且定量或半定量(DLR:41-650 ng mL(-1))兼容。该方法的检测结果与gE特异性PCR的结果一致,表明该基于SERS的侧向流动测定法可以用作鉴别野生型PRV和gE缺失疫苗的新工具。

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