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利用环介导等温DNA扩增技术(LAMP)检测小麦粒中稻腥黑粉菌、光腥黑粉菌和矮腥黑粉菌的污染情况。

Detection of Tilletia caries, Tilletia laevis and Tilletia controversa wheat grain contamination using loop-mediated isothermal DNA amplification (LAMP).

作者信息

Pieczul Katarzyna, Perek Agnieszka, Kubiak Krzysztof

机构信息

Institute of Plant Protection - National Research Institute, Władysława Węgorka, Poznań 2060-318, Poland.

出版信息

J Microbiol Methods. 2018 Nov;154:141-146. doi: 10.1016/j.mimet.2018.10.018. Epub 2018 Oct 28.

Abstract

The study describes a novel diagnostic protocol based on a loop-mediated isothermal DNA amplification (LAMP) for identification of wheat grains infection by Tilletia laevis, Tilletia caries (common bunt) and Tilletia controversa (draft bunt). The presented data showed that the LAMP analysis is a simple, specific and rapid method that could be used for detection of Tilletia spp. in contaminated grain samples. The lowest DNA concentration required for the successful detection of Tilletia spp. strains were estimated to be 0.001 ng/μl. Simultaneously the detection limit for wheat grain contamination by T. caries and T. laevis teliospores was estimated at 20 μg per 100 g of grain. For T. controversa detection limit was lower and was approximately 20 mg of teliospores per 100 g of grain. The negative results of the LAMP reactions were achieved for the most common fungal species colonizing wheat grain like Fusarium spp., Alternaria sp., Cladosporium sp., Helminthosporium sp., and Penicillium sp.

摘要

该研究描述了一种基于环介导等温DNA扩增(LAMP)的新型诊断方案,用于鉴定小麦粒是否受到光腥黑粉菌、网腥黑粉菌(普通腥黑穗病)和矮腥黑粉菌(矮化腥黑穗病)的感染。所呈现的数据表明,LAMP分析是一种简单、特异且快速的方法,可用于检测受污染谷物样本中的腥黑粉菌属。成功检测腥黑粉菌属菌株所需的最低DNA浓度估计为0.001 ng/μl。同时,网腥黑粉菌和光腥黑粉菌冬孢子对小麦粒污染的检测限估计为每100 g谷物20 μg。对于矮腥黑粉菌,检测限较低,约为每100 g谷物20 mg冬孢子。对于定殖在小麦粒上的最常见真菌物种,如镰刀菌属、链格孢属、枝孢属、长蠕孢属和青霉属,LAMP反应均得到阴性结果。

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