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A more sensitive and rapid multiplex RT-PCR assay combining with magnetic nanobeads for simultaneous detection of viruses in sweet potato

机译:结合磁性纳米珠的更灵敏,快速的多重RT-PCR测定法,可同时检测甘薯中的病毒

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摘要

An improved multiplex RT-PCR assay combined with magnetic nanobeads (MNB-RT-PCR) was developed for simultaneous detection of four sweet potato viruses, Sweet potato virus G (SPVG), Sweet potato feathery mottle virus (SPFMV), Sweet potato virus C (SPVC) and Sweet potato chlorotic fleck virus (SPCFV). Four primer pairs specific for each virus were designed and the corresponding PCR products were 169, 357, 516 and 900 bp in length for SPVG, SPFMV, SPVC and SPCFV, respectively. The specificity of the method was tested using different combinations of virus templates, and the identities of the amplification products were confirmed by sequencing. The limits of detection for all four viruses by single and multiplex MNB-RT-PCR assays were comparable. The assay was further evaluated using laboratory and field samples compared with a conventional CTAB-RT-PCR assay, and the comparative results showed that the MNB-RT-PCR assay was more rapid and sensitive. These results suggest that the multiplex MNB-RT-PCR assay is an effective and preferable method for virus detection in sweet potato
机译:建立了一种改进的与磁性纳米珠相结合的多重RT-PCR分析方法(MNB-RT-PCR),用于同时检测四种甘薯病毒,甘薯病毒G(SPVG),甘薯羽毛斑驳病毒(SPFMV),甘薯病毒C (SPVC)和红薯褪绿斑点病毒(SPCFV)。设计了对每种病毒特异的四个引物对,相应的PCR产物的SPVG,SPFMV,SPVC和SPCFV的长度分别为169、357、516和900 bp。使用病毒模板的不同组合测试了该方法的特异性,并通过测序确认了扩增产物的身份。通过单次和多重MNB-RT-PCR分析对所有四种病毒的检测限是可比较的。与常规CTAB-RT-PCR分析相比,使用实验室和野外样品进一步评估了该分析,比较结果表明MNB-RT-PCR分析更快速,更灵敏。这些结果表明,多重MNB-RT-PCR检测是检测甘薯中病毒的有效且优选的方法

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