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首页> 外文期刊>Journal of Virological Methods >Use of dried high-phenolic laden host leaves for virus and viroid preservation and detection by PCR methods.
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Use of dried high-phenolic laden host leaves for virus and viroid preservation and detection by PCR methods.

机译:使用干燥的高酚满载宿主叶进行病毒和类病毒的保存以及通过PCR方法检测。

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摘要

The efficiency of RNA extraction for Apricot latent virus (ApLV), Plum bark necrosis stem pitting associated virus (PBNSPaV), Prunus necrotic ring spot virus (PNRSV), Potato virus Y (PVY), and Apple scar skin viroid (ASSVd) from infected hosts is of great importance for molecular diagnosis by the polymerase chain reaction (PCR). A method is described for drying tissue to overcome phenolic inhibitors of viral RNA. This study showed that the infected host leaves, dried at 65 degrees C for 2 days and conserved at 4 degrees C in air proof conditions, serve as good sources for detection of viral and viroid pathogens by PCR methods. Preliminary results suggest that ApLV, PNRSV, PVY, and ASSVd were detected easily by reverse transcriptase-polymerase chain reaction (RT-PCR) and PBNSPaV by nested-RT-PCR with high amplification yields. No significant difference was observed between ethidium bromide-stained band profiles of dried compared to fresh leaves of infected samples. The RNA derived from dry leaf samples was suitable for detection studies. This simple and inexpensive method has proved very effective for long term conservation of virus and viroid isolates.
机译:RNA提取受感染的杏潜伏病毒(ApLV),李子树皮坏死茎凹陷相关病毒(PBNSPaV),李属坏死环斑病毒(PNRSV),马铃薯病毒Y(PVY)和苹果疤痕皮肤类病毒(ASSVd)的效率宿主对于通过聚合酶链反应(PCR)进行分子诊断非常重要。描述了一种用于干燥组织以克服病毒RNA的酚类抑制剂的方法。这项研究表明,感染的寄主叶片在65摄氏度下干燥2天,并在4摄氏度的空气条件下保存,是通过PCR方法检测病毒和类病毒病原体的良好来源。初步结果表明,通过逆转录酶-聚合酶链反应(RT-PCR)和PBNSPaV可以通过巢式RT-PCR轻松检测到ApLV,PNRSV,PVY和ASSVd,且扩增率很高。与感染样品的新鲜叶子相比,干燥的溴化乙锭染色的条带图谱之间没有观察到显着差异。从干叶样品中提取的RNA适用于检测研究。事实证明,这种简单且廉价的方法对于长期保存病毒和类病毒分离株非常有效。

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