College of Plant Protection, Jilin Agricultural University, Changchun 130118, China.
Engineering Research Center of Natural Enemies, Institute of Biological Control, Jilin Agricultural University, Changchun 130118, China.
Plant Dis. 2024 Jun;108(6):1461-1469. doi: 10.1094/PDIS-10-23-2101-SR. Epub 2024 May 22.
Northern corn leaf blight (NCLB), caused by , is one of the most devastating foliar diseases of maize. Rapid and accurate diagnosis for this disease is urgently needed but still limited. Here, we establish a field-deployable diagnostic method to detect based on loop-mediated isothermal amplification (LAMP) assays. A software application called K-mer Elimination by Cross-reference was used to search for the specific sequences belonging to by comparing the whole genome sequence between and other known maize pathogens. Five LAMP primer sets were designed based on specific and single-copy fragments of . Post-LAMP analyses indicated that only the primer set, Et9468_set1, was the most suitable, producing a ladder-like amplification pattern in the agarose gel electrophoresis and a strong fluorescence signal in the presence of SYBR Green I. The LAMP assay using Et9468_set1 primers demonstrated a high level of specificity in distinguishing from six other common fungal pathogens of maize, as well as 12 more fungal and oomycete strains including the epiphytic fungi from maize leaves and other crop pathogens. Moreover, it exhibited remarkable sensitivity by detecting five copies per reaction, which was approximately 10 times more sensitive compared with conventional PCR. The LAMP assay successfully detected in field maize leaves without DNA extraction, demonstrating its suitability for rapid on-spot detection of NCLB. Our study provides a direct LAMP diagnostic method to detect , which enables on-site pathogen detection in the field and the development of preventive strategies for NCLB management.
北方玉米叶枯病(NCLB)由 引起,是玉米最具破坏性的叶部病害之一。快速准确地诊断这种疾病是迫切需要的,但仍然有限。在这里,我们建立了一种基于环介导等温扩增(LAMP)分析的现场可部署诊断方法来检测 。通过比较 与其他已知玉米病原体之间的全基因组序列,使用名为“通过交叉引用消除 K-mer”的软件应用程序搜索属于 的特定序列。基于 的特异和单拷贝片段设计了五个 LAMP 引物组。LAMP 分析后表明,只有引物组 Et9468_set1 是最适合的,在琼脂糖凝胶电泳中产生梯状扩增模式,并且在存在 SYBR Green I 时产生强荧光信号。使用 Et9468_set1 引物的 LAMP 检测方法在区分 与其他六种常见玉米真菌病原体以及包括玉米叶片上的附生真菌和其他作物病原体在内的 12 种更多真菌和卵菌菌株方面表现出高度特异性。此外,它的检测灵敏度非常高,可检测到每个反应五个拷贝,比常规 PCR 灵敏约 10 倍。LAMP 检测方法无需 DNA 提取即可成功检测田间玉米叶片中的 ,证明其适用于快速现场检测 NCLB。我们的研究提供了一种直接的 LAMP 诊断方法来检测 ,这使得能够在现场进行病原体检测,并制定 NCLB 管理的预防策略。