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A Loop-Mediated Isothermal Amplification Assay for Rapid Detection of Pectobacterium aroidearum that Causes Soft Rot in Konjac

机译:快速检测导致魔芋软腐的无胶油菌的环介导的等温扩增测定

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摘要

Bacterial soft rot caused by Pectobacterium species is a serious disease in konjac (Amorphophallus konjac), a healthy source of starch particularly in East Asia. An effective diagnostic method is crucial to control the disease and reduce losses in konjac production. In this study, we evaluated a loop-mediated isothermal amplification (LAMP) assay with a specific primer set for the rapid and accurate detection of P. aroidearum. A comparative genomics approach was used to identify the specific genes suitable for the design of LAMP primers. The candidate target genes were determined through a first-round comparison with a 50-genome nucleotide database, and subjected to a second-round screening with the GenBank NR database. As a result, nine specific genes of P. aroidearum were selected for LAMP primer design. After screening of the primers, the primer set 1675-1 was chosen for LAMP detection owing to its high specificity and sensitivity. The LAMP assay could detect the presence of P. aroidearum genomic DNA at a concentration as low as 50 fg and 1.2 × 104 CFU/g artificially infected soil within 40 min at 65 °C. Subsequently, this primer set was successfully used to specifically detect P. aroidearum in naturally infected and non-symptomatic plant samples or soil samples from the field. This study indicates that a comparative genomic approach may facilitate the development of highly specific primers for LAMP assays, and a LAMP diagnostic assay with the specific primer set 1675-1 should contribute to the rapid and accurate detection of soft-rot disease in konjac at an early stage.
机译:果胶杆菌引起的细菌性软腐病是魔芋中的一种严重疾病,魔芋是健康的淀粉来源,尤其是在东亚。有效的诊断方法对于控制疾病和减少魔芋生产的损失至关重要。在这项研究中,我们评估了具有特定引物组的环介导的等温扩增(LAMP)分析,以快速,准确地检测无冠假单胞菌。比较基因组学方法用于鉴定适合于LAMP引物设计的特定基因。通过与50个基因组核苷酸数据库的第一轮比较确定候选目标基因,并通过GenBank NR数据库进行第二轮筛选。结果,选择了九种P.apearearum特异基因进行LAMP引物设计。筛选引物后,由于其高特异性和敏感性,选择了用于LAMP检测的引物组1675-1。 LAMP法可在65°C的40分钟内检测到浓度低至50 fg和1.2×10 4 CFU / g人工感染土壤的无冠假单胞菌基因组DNA。随后,该引物组成功用于特异性检测自然感染和无症状植物样品或田间土壤样品中的无冠假单胞菌。这项研究表明,比较基因组学方法可能有助于开发用于LAMP测定的高度特异性引物,并且具有1675-1特异性引物对的LAMP诊断测定应有助于快速准确地检测魔芋中的软腐病。早期。

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