Department of Studies in Biotechnology, Asian Seed Health Centre, University of Mysore, Manasagangotri, Mysore 570006, Karnataka, India.
Arch Microbiol. 2012 Nov;194(11):923-32. doi: 10.1007/s00203-012-0826-x. Epub 2012 Jun 22.
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.
黄萎轮枝菌是一种重要的种子携带致病性真菌,可导致向日葵枯萎病。目前的检测方法基于培养和形态鉴定,既费时费力,又不一定可靠。本研究基于黄萎轮枝菌的核糖体 RNA 基因(rDNA)重复区的 5.8S RNA 基因和内部转录间隔区-ITS1 和 ITS2 的序列数据,设计了种特异性引物,建立了基于 PCR 的诊断方法。通过对从印度分离的 18 株黄萎轮枝菌、14 株非靶标链格孢属真菌和 11 株其他属真菌分离物的 DNA 进行 PCR 分析,验证了引物对 AhN1F 和 AhN1R 的特异性。从黄萎轮枝菌分离物的 DNA 中检测到 357-bp 的单一扩增产物。与测试的其他任何分离物均未观察到交叉反应。PCR 方法的检测限为模板 DNA 的 10pg。该引物还可以检测感染向日葵种子中的病原体。与传统方法相比,该种特异性 PCR 方法为黄萎轮枝菌的检测和鉴定提供了一种快速、简单、强大和可靠的替代方法。这是首次报道黄萎轮枝菌特异性引物组。