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Separation of endogenous viral elements from infectious Penaeus stylirostris densovirus using recombinase polymerase amplification

机译:用重组酶聚合酶扩增法分离猪传染性对虾线粒体病毒的内源性病毒成分

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摘要

Non-infectious Penaeus stylirostris densovirus (PstDV)-related sequences in the shrimp genome cause false positive results with current PCR protocols. Here, we examined and mapped PstDV insertion profile in the genome of Australian Penaeus monodon. A DNA sequence which is likely to represent infectious PstDV was also identified and used as a target sequence for recombinase polymerase amplification (RPA)-based approach, developed for specifically detecting PstDV. The RPA protocol at 37 degrees C for 30 min showed no cross-reaction with other shrimp viruses, and was 10 times more sensitive than the 309F/R PCR protocol currently recommended by the World Organization for Animal Health (OIE) for PstDV diagnosis. These features, together with the simplicity of the protocol, requiring only a heating block for the reaction, offer opportunities for rapid and efficient detection of PstDV. (C) 2014 Elsevier Ltd. All rights reserved.
机译:虾基因组中非感染性对虾对虾病毒(PstDV)相关序列在当前的PCR方案中导致假阳性结果。在这里,我们检查并绘制了澳大利亚斑节对虾基因组中的PstDV插入图谱。还鉴定了可能代表传染性PstDV的DNA序列,并将其用作基于重组酶聚合酶扩增(RPA)的方法的靶序列,该方法已开发用于特异性检测PstDV。 RPA协议在37°C持续30分钟时未显示与其他虾类病毒的交叉反应,并且比目前由世界动物卫生组织(OIE)推荐用于PstDV诊断的309F / R PCR协议高10倍。这些功能以及操作流程的简单性,只需一个加热块即可进行反应,为快速,有效地检测PstDV提供了机会。 (C)2014 Elsevier Ltd.保留所有权利。

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