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首页> 外文期刊>Archives of microbiology >Specific PCR-based detection of Alternaria helianthi: the cause of blight and leaf spot in sunflower.
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Specific PCR-based detection of Alternaria helianthi: the cause of blight and leaf spot in sunflower.

机译:基于PCR的特异链格孢菌检测:向日葵中枯萎和叶斑的原因。

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摘要

Alternaria helianthi is an important seed-borne pathogenic fungus responsible for blight disease in sunflower. The current detection methods, which are based on culture and morphological identification, are time-consuming, laborious and are not always reliable. A PCR-based diagnostic method was developed with species-specific primers designed based on the sequence data of a region consisting of the 5.8S RNA gene and internal transcribed spacers-ITS 1 and ITS 2 of nuclear ribosomal RNA gene (rDNA) repeats of A. helianthi. The specificity of the primer pairs AhN1F and AhN1R designed was verified by PCR analysis of DNA from 18 Alternaria helianthi strains isolated from India, 14 non-target Alternaria spp. and 11 fungal isolates of other genera. A single amplification product of 357-bp was detected from DNA of A. helianthi isolates. No cross-reaction was observed with any of the other isolates tested. The detection limit of the PCR method was of 10?pg from template DNA. The primers could also detect the pathogen in infected sunflower seed. This species-specific PCR method provides a quick, simple, powerful and reliable alternative to conventional methods in the detection and identification of A. helianthi. This is the first report of an A. helianthi-specific primer set.
机译:向日葵链格孢是一种重要的种子传播性病原真菌,可引起向日葵的枯萎病。当前基于培养物和形态学鉴定的检测方法既费时,费力又并不总是可靠的。基于物种的特异性引物,开发了一种基于PCR的诊断方法,该引物基于由5.8S RNA基因和A核糖体RNA基因(rDNA)重复序列的内部转录间隔子ITS 1和ITS 2组成的区域的序列数据而设计向日葵通过PCR分析来自印度的14个非靶标链格孢菌的18种链格孢菌的DNA的PCR分析,验证了设计的引物对AhN1F和AhN1R的特异性。和其他属的11种真菌分离株。从Helianthi分离株的DNA中检测到357bp的单个扩增产物。与测试的任何其他分离物均未观察到交叉反应。 PCR方法的检测限为模板DNA的10µpg。引物还可以检测受感染向日葵种子中的病原体。这种特定于物种的PCR方法在检测和鉴定A. helianthi中提供了一种常规方法的快速,简单,强大和可靠的替代方法。这是A. helianthi特异性引物对的首次报道。

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