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一种用于区分伪狂犬病病毒野生分离株和gE缺失疫苗株的等温重组酶聚合酶测定法与侧向流动试纸条联用

An isothermal recombinase polymerase assay coupled with lateral flow dipstick for differentiation of pseudorabies virus wild isolates and gE-deleted vaccine strains.

作者信息

Ma L, Wang Y, Wang X, Zhang M, Zhu M

机构信息

School of Biotechnology and Food Engineering, Anyang Institute of Technology, Anyang, China.

出版信息

Pol J Vet Sci. 2024 Dec;27(4):621-630. doi: 10.24425/pjvs.2024.152952.

Abstract

Pseudorabies virus (PRV) is one of the most important infectious diseases which leads to significant economic losses in the global swine industry. The gE-deleted vaccine is widely used to prevent susceptible pigs from PRV infection. There is no report of the differentiation of PRV wild strain and vaccine strain by recombinase polymerase amplification (RPA) coupled with a lateral flow dipstick (LFD) method. In the present study, the gD and gE gene-targeted primer-probe sets were designed. The RPA-LFD assay could discriminate between the PRV wild strain and the vaccine strain. The RPA reaction conditions were also evaluated. The optimal reaction temperature and reaction time for the RPA-LFD assay were 37℃ and 20 min. The detection limit was 10 genome copies per reaction for PRV wild strain and gE-deleted vaccine strain. The assay did not have cross-reaction with other common swine viral pathogens. The effectiveness of the RPA-LFD assay for detecting the clinical samples was evaluated by testing 80 samples. The result of the assay was compared with that of the conventional PCR. The positive rate of PRV wild strain by the RPA-LFD assay was 20%, whereas the positive rate of PRV wild strain by the PCR assay was 18.8%. The assay therefore provides a novel alternative for differentiation of PRV wild strain and vaccine strain.

摘要

伪狂犬病病毒(PRV)是导致全球养猪业重大经济损失的最重要传染病之一。缺失gE基因的疫苗被广泛用于预防易感猪感染PRV。目前尚无关于通过重组酶聚合酶扩增(RPA)结合侧向流动试纸条(LFD)方法区分PRV野毒株和疫苗株的报道。在本研究中,设计了靶向gD和gE基因的引物-探针组。RPA-LFD检测方法能够区分PRV野毒株和疫苗株。同时还评估了RPA反应条件。RPA-LFD检测方法的最佳反应温度和反应时间分别为37℃和20分钟。PRV野毒株和缺失gE基因的疫苗株的检测限均为每个反应10个基因组拷贝。该检测方法与其他常见猪病毒病原体无交叉反应。通过检测80份临床样本评估了RPA-LFD检测方法检测临床样本的有效性。将该检测方法的结果与传统PCR的结果进行了比较。RPA-LFD检测方法检测PRV野毒株的阳性率为20%,而PCR检测方法检测PRV野毒株的阳性率为18.8%。因此,该检测方法为区分PRV野毒株和疫苗株提供了一种新的选择。

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