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Molecular detection of Cylindrocarpon destructans in infected Chinese ginseng roots and soil

机译:感染人参根和土壤中圆柱果皮的分子检测

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Ginseng (Panax ginseng?C.A. Meyer) is one of the most important medicinal plants in China, but its yields are often reduced by a variety of root pathogens. The root rot of ginseng is a destructive soil-borne disease caused by?Cylindrocarpon destructans(teleomorph:?Neonectria radicicola). A species-specific polymerase chain reaction (PCR) assay was developed for rapid detection of?C. destructans?in diseased ginseng roots and artificially inoculated soil. One pair of specific primers was designed from comparisons of nucleotide sequences of the nuclear ribosomal internal transcribed spacer (ITS) regions of 22 fungal isolates from northeast of China. Under stringent PCR conditions, primers CD-F and CD-R amplified only a 450 bp fragment from?C. destructans?DNA but not from other pathogens or negative control. The sensitivity of detection was 1 pg genomic DNA per 25 μl PCR reaction volume, and?C. destructanscould be specifically detected with CD-F/CD-R from infected ginseng roots and soil. The approach outlined here could be further utilized as a rapid and reliable tool for the diagnosis and monitoring of the root rot of ginseng.
机译:人参(Panax ginseng?C.A。Meyer)是中国最重要的药用植物之一,但其产量常常因各种根部病原体而降低。人参的根腐病是一种破坏性的土传疾病,由“ Cylindrocarpon destructans”(teleomorph:“ Neonectria radicicola”)引起。建立了一种物种特异性聚合酶链反应(PCR)测定法,用于快速检测?C。人参根部和人工接种的土壤中含有“ destructans”。通过比较来自中国东北的22种真菌分离株的核糖体内部转录间隔区(ITS)区域的核苷酸序列,设计了一对特异性引物。在严格的PCR条件下,引物CD-F和CD-R仅从ΔC扩增了450bp的片段。而不是其他病原体或阴性对照的DNA。检测的灵敏度为每25μlPCR反应体积1 pg基因组DNA,以及?C。应该用受感染的人参根和土壤中的CD-F / CD-R特异性地检测到破坏结构。这里概述的方法可以进一步用作诊断和监测人参根腐病的快速可靠的工具。

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