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High sensitive method detection of plant RNA viruses by Electrochemiluminescence reverse transcription PCR

机译:化学发光逆转录PCR高灵敏度检测植物RNA病毒

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摘要

It is well known that plant and animal viruses had widely spread the whole of world, and made a big loss in farming and husbandry. It is necessary that a highly efficient and accurate virus's detection method was developed. This research combines reverse transcription polymerase chain reaction (RT-PCR) technique with electrochemiluminescence method, to detect plant RNA viruses for the first time. Biotin-probe hybridizes with PCR product to specific select the target for detection, thus can avoid pseudo-positive result. TBR-probe hybridizes with PCR product to emit light for ECL detection. Specific nucleic acid sequences (20bp) were added to 5' terminal all of the primers, which can improve the chance of hybridization between TBR-probe and PCR product. At the same time, one of the PCR product chain can hybridize two Ru-probes, the ECL signal is intensified. The method was used to detect Odntoglossum ringspot virus ORSV, Sugarcane mosaic virus ScMV, Sorghum mosaic virus SrMV, and Maize dwarf mosaic virus MDMV, the experiment results show that this method could reliably identity virus infected plant samples. In a word, this method has higher sensitivity and lower cost than others. It can effectively detect the plant viruses with simplicity, stability, and high sensitivity.
机译:众所周知,动植物病毒已在全世界广泛传播,给农牧业造成了巨大损失。有必要开发一种高效,准确的病毒检测方法。这项研究结合了逆转录聚合酶链反应(RT-PCR)技术和电化学发光方法,首次检测到植物RNA病毒。生物素探针与PCR产物杂交,可以特异性地选择要检测的靶标,从而避免了假阳性结果。 TBR探针与PCR产物杂交以发光以进行ECL检测。将特异性核酸序列(20bp)添加到所有引物的5'末端,这可以提高TBR探针与PCR产物之间杂交的机会。同时,一条PCR产物链可以杂交两个Ru探针,增强了ECL信号。该方法用于检测犬牙牙rings环斑病毒ORSV,甘蔗花叶病毒ScMV,高粱花叶病毒SrMV和玉米矮花叶病毒MDMV,实验结果表明该方法能够可靠地鉴定被病毒感染的植物样品。总之,该方法比其他方法具有更高的灵敏度和更低的成本。它可以简单,稳定和高灵敏度地有效检测植物病毒。

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