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实时荧光定量PCR检测与鉴别南方玉米锈病菌和普通玉米锈病菌多堆柄锈菌和高粱柄锈菌

Real-Time PCR Detection and Discrimination of the Southern and Common Corn Rust Pathogens Puccinia polysora and Puccinia sorghi.

作者信息

Crouch Jo Anne, Szabo Les J

机构信息

United States Department of Agriculture-Agricultural Research Service (USDA-ARS), Cereal Disease Laboratory, University of Minnesota, St. Paul 55108.

出版信息

Plant Dis. 2011 Jun;95(6):624-632. doi: 10.1094/PDIS-10-10-0745.

Abstract

Over the past several years, southern corn rust (SCR) outbreaks caused by the fungus Puccinia polysora have become increasingly problematic for corn growers in the United States. SCR is currently diagnosed through the visual examination of disease symptoms and pathogen morphology, including pigmentation, size, shape, and location of fruiting structures. However, these characteristics are similar to those produced by the common corn rust fungus P. sorghi, confounding accurate visual diagnosis of SCR. Here we report the development of a real-time polymerase chain reaction assay that discriminates between P. polysora and P. sorghi. Sequences of the rDNA internal transcribed spacer region were determined for P. polysora and P. sorghi. 5-Carboxyfluorescein fluorophore-labeled hydrolysis probes that differed at 14 nucleotide positions between the species were developed from these data and used to screen DNA extracted directly from rust-infected corn leaves. Species-specific, reproducible identifications of the pathogens were made from as little as 50 pg of DNA within 30 min, and were reliably performed from both recent collections and herbarium specimens. This assay will be useful for rapid and accurate diagnosis of SCR, and could serve as a tool to monitor the distribution and incidence of the disease in the United States.

摘要

在过去几年中,由真菌多堆柄锈菌(Puccinia polysora)引起的南方玉米锈病(SCR)疫情给美国玉米种植者带来了越来越多的问题。目前,SCR是通过对病害症状和病原体形态进行目视检查来诊断的,包括色素沉着、大小、形状和产孢结构的位置。然而,这些特征与常见玉米锈菌高粱柄锈菌(P. sorghi)产生的特征相似,这使得对SCR的准确目视诊断变得困难。在此,我们报告了一种能区分多堆柄锈菌和高粱柄锈菌的实时聚合酶链反应检测方法的开发。测定了多堆柄锈菌和高粱柄锈菌的核糖体DNA内转录间隔区序列。根据这些数据开发了在这两个物种之间14个核苷酸位置不同的5-羧基荧光素荧光团标记的水解探针,并用于直接从感染锈病的玉米叶片中提取的DNA的筛选。在30分钟内,从低至50 pg的DNA中就能对病原体进行物种特异性的、可重复的鉴定,并且对近期采集的样本和植物标本馆标本都能可靠地进行鉴定。该检测方法将有助于快速准确地诊断SCR,并可作为监测该疾病在美国的分布和发病率的工具。

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