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首页> 外文期刊>Annals of Applied Biology >Molecular detection of Colletotrichum falcatum causing red rot disease of sugarcane (Saccharum officinarum) using a SCAR marker.
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Molecular detection of Colletotrichum falcatum causing red rot disease of sugarcane (Saccharum officinarum) using a SCAR marker.

机译:使用SCAR标记分子检测导致甘蔗红腐病( Saccharum officinarum )红腐病的Coletotrichum falcatum

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摘要

Red rot disease of sugarcane caused by Colletotrichum falcatum is one of the most destructive diseases of sugarcane (Saccharum officinarum) worldwide. The pathogen spreads primarily through infected sugarcane setts and hence the use of disease-free planting materials is essential for preventing disease development in the field. In the present study a polymerase chain reaction (PCR) assay was developed for accurate and sensitive detection of C. falcatum in planting materials. Randomly amplified polymorphic DNA (RAPD) analysis identified a 566 bp PCR fragment that was specific to C. falcatum. The DNA sequence of this fragment was determined and used to design oligonucleotides amplifying a 442 bp sequence characterised amplified region (SCAR). The specificity of the SCAR primers was evaluated using purified DNA from C. falcatum and other Colletotrichum spp. as templates in PCR. The results indicated that the SCAR primers were highly specific to C. falcatum since the 442 bp fragment was amplified only from DNA of isolates and races of C. falcatum but not from any other Colletotrichum spp. tested. The detection sensitivity of C. falcatum was 0.1 ng for genomic DNA of C. falcatum and 5 ng for DNA extracted from infected sugarcane tissue. This new PCR-based assay is a convenient tool for detection of this important pathogen in seed canes to ensure production of sugarcane.
机译:Colletotrichum falcatum 引起的甘蔗红腐病是全球最具破坏力的甘蔗( Saccharum officinarum )疾病之一。病原体主要通过受感染的甘蔗定居点传播,因此,使用无病的种植材料对于防止田间疾病的发展至关重要。在本研究中,开发了用于精确和灵敏地检测C的聚合酶链反应(PCR)分析方法。种植材料中的falcatum 。随机扩增的多态性DNA(RAPD)分析鉴定了一个566 bp的PCR片段,该片段对C特异。 falcatum 。确定该片段的DNA序列,并将其用于设计扩增442bp特征序列的扩增区域(SCAR)的寡核苷酸。使用来自iC的纯化DNA评估SCAR引物的特异性。 falcatum 和其他 Colletotrichum spp。作为PCR中的模板。结果表明,SCAR引物对iC具有高度特异性。 falcatum 因为442 bp的片段仅从 C的分离株和小种的DNA中扩增而来。 falcatum ,但不是来自其他 Colletotrichum spp。经过测试。 i C的检测灵敏度。对于 C的基因组DNA,法则含量为0.1 ng。从被感染的甘蔗组织中提取的DNA含量为5 ng。这种基于PCR的新检测方法是检测种子甘蔗中重要病原体以确保甘蔗生产的便捷工具。

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