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Simple and rapid method for routine screening of bovine leukemia virus by loop-mediated isothermal amplification assay

机译:环介导的等温扩增法简便快速地常规筛查牛白血病病毒

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摘要

Various techniques for screening and detection of bovine leukemia virus (BLV) were compared to ascertain a rapid and simple technique for routine examination. The performance of real-time PCR, nested PCR and loop-mediated isothermal amplification (LAMP) assays was compared using DNA extracted from whole blood instead of white blood cells (WBCs) of 23 cattle. Real-time PCR, LAMP and nested PCR detected 18, 16 and 11 BLV-positive cattle, respectively. These results suggest that LAMP using DNA from whole blood could enable rapid examination, as isolation of WBCs and electrophoresis is time-consuming and could be useful as a simple and rapid method for routine screening of BLV.
机译:比较了各种筛选和检测牛白血病病毒(BLV)的技术,以确定常规检查的快速简便的技术。使用从23头牛的全血而非白细胞(WBC)中提取的DNA对实时PCR,巢式PCR和环介导的等温扩增(LAMP)分析的性能进行了比较。实时PCR,LAMP和巢式PCR分别检测到18、16和11个BLV阳性牛。这些结果表明,使用LAMP从全血中提取DNA可以进行快速检查,因为白细胞分离和电泳非常耗时,可以作为常规筛查BLV的简便方法。

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