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一种用于快速检测导致魔芋软腐病的的环介导等温扩增检测方法。

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

机构信息

The Key Lab of Plant Pathology of Hubei Province, Huazhong Agricultural University, Wuhan 430070, China.

Yichang Academy of Agricultural Science, Yichang 443004, China.

出版信息

Int J Mol Sci. 2019 Apr 19;20(8):1937. doi: 10.3390/ijms20081937.

Abstract

Bacterial soft rot caused by species is a serious disease in 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 . 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 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 genomic DNA at a concentration as low as 50 fg and 1.2 × 10 CFU/g artificially infected soil within 40 min at 65 °C. Subsequently, this primer set was successfully used to specifically detect 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.

摘要

种引起的细菌性软腐病是魔芋()的一种严重疾病,魔芋是东亚地区特别是淀粉的健康来源。一种有效的诊断方法对于控制疾病和减少魔芋生产损失至关重要。在本研究中,我们评估了一种使用特定引物组的环介导等温扩增(LAMP)检测法,用于快速准确地检测。采用比较基因组学方法鉴定适合设计 LAMP 引物的特定基因。通过与 50 个基因组核苷酸数据库的第一轮比较确定候选靶基因,并使用 GenBank NR 数据库进行第二轮筛选。结果,选择了 种的 9 个特异性基因用于 LAMP 引物设计。在筛选引物后,由于其高特异性和灵敏度,选择了引物 1675-1 用于 LAMP 检测。LAMP 检测可以在 65°C 下 40 分钟内检测到低至 50 fg 和 1.2×10 CFU/g 人工感染土壤中存在的 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本或田间土壤样本中的 。本研究表明,比较基因组学方法可能有助于开发用于 LAMP 检测的高度特异性引物,并且使用特异性引物 1675-1 的 LAMP 诊断检测法应该有助于在早期快速准确地检测魔芋软腐病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a994/6514923/589c67bd72db/ijms-20-01937-g001.jpg

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