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首页> 外文期刊>Archives of virology >Rapid detection of bovine herpesvirus 1 in bovine semen by loop-mediated isothermal amplification (LAMP) assay
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Rapid detection of bovine herpesvirus 1 in bovine semen by loop-mediated isothermal amplification (LAMP) assay

机译:通过环介导的等温扩增(LAMP)分析快速检测牛精液中的牛疱疹病毒1

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Bovine herpesvirus 1 (BoHV-1) is the most common viral pathogen found in bovine semen, causing numerous reproductive disorders leading to economic losses to the cattle industry. For rapid detection of BoHV-1 in bovine semen, in this study, we applied a loop-mediated isothermal amplification (LAMP) assay. The assay could be completed within 90 min, including total DNA isolation, target amplification, and visual interpretation of positive or negative results with the naked eye. The assay detected as little as 10 fg of BoHV-1 DNA per reaction. The analytical sensitivity of the assay was 0.2 TCID50 BoHV-1 per reaction, which was 100 times more sensitive than conventional PCR and comparable to TaqMan real-time PCR. The applicability of the assay was assessed by analysing 118 semen samples collected from breeding bulls. On comparison with TaqMan real-time PCR, the LAMP assay had a diagnostic sensitivity of 97 %, specificity of 100 %, and accuracy of 99.2 % for detection of BoHV-1 in bovine semen. The LAMP assay developed in this study is a rapid, sensitive, and cost-effective alternative for detection of BoHV-1 in bovine semen.
机译:牛疱疹病毒1(BoHV-1)是在牛精液中发现的最常见的病毒病原体,它引起许多繁殖障碍,给养牛业造成经济损失。为了快速检测牛精液中的BoHV-1,在这项研究中,我们应用了环介导的等温扩增(LAMP)分析。该测定可在90分钟内完成,包括总DNA分离,靶标扩增以及用肉眼目测对阳性或阴性结果的观察。该测定每个反应可检测到低至10 fg的BoHV-1 DNA。该方法的分析灵敏度为每个反应0.2 TCID50 BoHV-1,比常规PCR灵敏度高100倍,与TaqMan实时PCR相当。通过分析从种公牛收集的118份精液样品,评估了该测定方法的适用性。与TaqMan实时PCR相比,LAMP测定法对牛精液中BoHV-1的诊断灵敏度为97%,特异性为100%,准确度为99.2%。在这项研究中开发的LAMP测定法是一种快速,灵敏且经济高效的替代方法,可用于检测牛精液中的BoHV-1。

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