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我国甜菜褐斑病菌的PCR快速检测

Rapid detection of Cercospora leaf spot fungus in sugar beet using specific Cebe2 primers in China

中文摘要英文摘要

甜菜褐斑病是甜菜生产中的世界性重要真菌病害之一,给甜菜生产造成严重的经济损失。由于其病原菌甜菜尾孢菌(Cercospora beticola)菌落形态、分生孢子形态变异较大,田间初期症状难判定,后期症状典型时往往已错过了最佳防治适期,因此,传统诊断方法存在一定缺陷。为筛选适宜的甜菜尾孢菌特异分子检测技术,本文对已报道的三种分子方法进行了比较,结果表明,由于尾孢属不同种病原菌的actin gene和rRNA-genes的ITS区同源性均较高,因而ITS及actin引物很难特异性地检测C. beticola,而利用引物Cebe2可以特异性地检测C. beticola,甚至可以检测出单一病斑的病原菌。同时,利用特异引物Cebe2对采集到的我国主要甜菜产区137份病样进行了检测,其中有119份样本检测到了C. beticola。本文选择的检测体系为C. beticola鉴定和病害发生的早期诊断提供了非常有效的方法。

ercospora leaf spot (CLS) in sugar beet causesd by Cercospora beticola is one of the major fungal diseases of sugar beet world-wide and causes a great economic loss for sugar beet production. It’s difficult to diagnose CLS with traditional method because of some variation of colony morphology and conidia, especially hardly diagnose the initial of field symptoms and it would miss the best control period when typical symptoms showed. For selection of suitable C.beticoa-specific molecular detection techniques, this paper has compared three kinds of the reported molecular methods. The results show that high homology of the coding region of the actin gene and the ITS-region of the rRNA-genes in genus Cercospora makes unambiguous identification and detection more complicated by amplied with primers ITS and actin. Fortunately, primer Cebe2 is sufficiently specific to identify and detect C. beticola even C. beticola from individual lesion. And 137 samples collected from the major sugar beet-producing areas across China were detected with the primer Cebe2, there are 119 samples positive to infection by C.beticola. In conclusion, the Cebe2 system provides a very effective method for identification of C. beticola and early diagnosis of CLS.

吴学宏、林杰、韩成贵、李大伟、任志山、于嘉林、刘梅

植物保护分子生物学植物学

甜菜尾孢菌引物Cebe2ITS区域肌动蛋白基因快速检测

ercospora beticolaprimers Cebe2ITS regionactin generapid detection

吴学宏,林杰,韩成贵,李大伟,任志山,于嘉林,刘梅.我国甜菜褐斑病菌的PCR快速检测[EB/OL].(2010-02-08)[2025-08-02].http://www.paper.edu.cn/releasepaper/content/201002-379.点此复制

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