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作 者:吴文涛 李梅云[2] 许姗姗 薛美静 张靖 魏环宇[1] 王扬[1] ]WU Wentao;LI Meiyun;XU Shanshan;XUE Meijing;ZHANG Jing;WEI Huanyu;WANG Yang(College of Plant Protection, Yunnan Agricultural University, Kunming, Yunnan 650201, China;Yunnan Academy of Agricultural Sciences of Tobacco, Kunming, Yunnan 650021, China)
机构地区:[1]云南农业大学植物保护学院,云南昆明650201 [2]云南省烟草农业科学研究院,云南昆明650021
出 处:《生物安全学报》2019年第1期59-64,共6页Journal of biosafety
基 金:口岸及边贸区;自贸区入侵生物本底调查与动态分布(2016YFC1202104);国家自然科学基金(31560502;311060361)
摘 要:【目的】建立一种基于环介导等温扩增(loop-mediated isothermal amplification,LAMP)技术,从植物罹病组织中直接检测3种常见的根结线虫,为根结线虫的监测和防治提供技术支持。【方法】分别采用3种根结线虫的种类特异性引物对所选择的根结线虫的DNA片段进行PCR扩增,扩增产物纯化、回收并测序。根据3种根结线虫的测序结果,针对种类特异区段,采用PrimerExplorerV4软件,分别设计3种根结线虫的LAMP引物。设计的引物组人工合成后,以提取的纯化种群线虫DNA为模板,分别进行引物组的特异性测试,筛选出分别针对3种根结线虫的最佳引物组。【结果】研究设计的3种根结线虫的LAMP特异性引物能够直接从植物根结中检测出南方、花生、爪哇3种常见根结线虫,LAMP快速检测体系为:dNTPS浓度为1 mmol·L^(-1),Mg^(2+)的浓度为5 mmol·L^(-1),不添加甜菜碱,反应时间为45 min。【结论】本实验建立的南方、花生、爪哇根结线虫LAMP快速分子检测方法,具有特异性强、灵敏度高、简单、快速、经济等特征,能够从罹病植物组织中快速准确地检测出南方、花生和爪哇根结线虫,具有极高的实践应用价值。【Aim】 The objective of this study is to establish a rapid diagnostic method for three species of root-knot nematode attacking plants based on the loop-mediated isothermal amplification (LAMP). This could provide technical support for monitoring and preventing the root-knot nematode infestation.【Method】 The DNA fragments of the selected root-knot nematodes were amplified by PCR using species-specific primers of the three root-knot nematodes. The amplified products were purified, recovered and sequenced. Based on the sequencing results of the three root-knot nematodes, three primers were designed using PrimerExplorerV4 software for species-specific segments. The designed primer sets were artificially synthesized, and the purified primer population DNA was used as a template to test the specificity of the primer sets. The best primer sets for three root-knot nematodes were selected.【Result】 The LAMP-specific primers of the three root-knot nematodes could directly detect the three common root-knot nematodes from the roots of plants, LAMP rapid detection system included 1 mmol·L ^-1 dNTPS, 5 mmol·L^-1 Mg^ 2+, without betaine, and at a reaction time of 45 min. The rapid detection of Meloidogyne incognita , Meloidogyne arenaria , Meloidogyne javanica by LAMP was assembled.【Conclusion】 The method was highly specific, sensitive, and economical, which made it possible for quick and accurate detection of M.incognita , M.arenaria and M.javanica from the infected plant root tissues, with high actual application value.
分 类 号:S432.45[农业科学—植物病理学]
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