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Development and Evaluation of a Novel and Rapid Detection Assay for Botrytis cinerea Based on Loop-Mediated Isothermal Amplification

机译:基于环介导的等温扩增的灰葡萄孢新型快速检测方法的开发和评估

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摘要

Botrytis cinerea is a devastating plant pathogen that causes grey mould disease. In this study, we developed a visual detection method of B. cinerea based on the Bcos5 sequence using loop-mediated isothermal amplification (LAMP) with hydroxynaphthol blue dye (HNB). The LAMP reaction was optimal at 63°C for 45 min. When HNB was added prior to amplification, samples with B. cinerea DNA developed a characteristic sky blue color after the reaction but those without DNA or with DNA of other plant pathogenic fungi did not. Results of HNB staining method were reconfirmed when LAMP products were subjected to gel electrophoresis. The detection limit of this LAMP assay for B. cinerea was 10−3 ng µL−1 of genomic DNA per reaction, which was 10-fold more sensitive than conventional PCR (10−2 ng µL−1). Detection of the LAMP assay for inoculum of B. cinerea was possible in the inoculated tomato and strawberry petals. In the 191 diseased samples, 180 (94.2%) were confirmed as positive by LAMP, 172 (90.1%) positive by the tissue separation, while 147 (77.0%) positive by PCR. Because the LAMP assay performed well in aspects of sensitivity, specificity, repeatability, reliability, and visibility, it is suitable for rapid detection of B. cinerea in infected plant materials prior to storage and during transportation, such as cut flowers, fruits and vegetables.
机译:灰葡萄孢是导致灰霉病的破坏性植物病原体。在这项研究中,我们开发了一种基于Bcos5序列的灰葡萄芽孢杆菌的视觉检测方法,使用了带有羟基萘酚蓝染料(HNB)的环介导的等温扩增(LAMP)。 LAMP反应在63℃下45分钟是最佳的。在扩增前加入HNB时,具有灰葡萄芽孢杆菌DNA的样品在反应后会呈现出特征性的天蓝色,而没有DNA或其他植物病原性真菌的DNA则没有。当对LAMP产品进行凝胶电泳时,可以再次确认HNB染色方法的结果。此灰质芽孢杆菌的LAMP测定的检测限是每个反应基因组DNA的10 −3 ng µL −1 ,比常规PCR灵敏度高10倍( 10 −2 ng µL −1 )。在接种的番茄和草莓花瓣中,可以检测到灰葡萄孢菌接种物的LAMP测定。在191个患病样本中,通过LAMP确认为阳性(180个,占94.2%),通过组织分离确认为172个(90.1%),而通过PCR确认为147(77.0%)。由于LAMP分析在敏感性,特异性,可重复性,可靠性和可见性方面表现良好,因此适合在存储和运输之前(如切花,水果和蔬菜)快速检测受感染植物材料中的灰霉病。

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