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利用环介导等温扩增技术快速诊断立枯丝核菌引起的大豆幼苗疫病和菜豆壳球孢引起的大豆炭腐病

Rapid Diagnosis of Soybean Seedling Blight Caused by Rhizoctonia solani and Soybean Charcoal Rot Caused by Macrophomina phaseolina Using LAMP Assays.

作者信息

Lu Chenchen, Song Bi, Zhang HaiFeng, Wang YuanChao, Zheng XiaoBo

机构信息

Department of Plant Pathology, College of Plant Protection, Nanjing Agricultural University, and Key Laboratory of Integrated Management of Crop Diseases and Pests, Ministry of Education, Nanjing 210095, China.

出版信息

Phytopathology. 2015 Dec;105(12):1612-7. doi: 10.1094/PHYTO-01-15-0023-R. Epub 2015 Nov 25.

Abstract

A new method of direct detection of pathogenic fungi in infected soybean tissues has been reported here. The method rapidly diagnoses soybean seedling blight caused by Rhizoctonia solani and soybean charcoal rot caused by Macrophomina phaseolina, and features loop-mediated isothermal amplification (LAMP). The primers were designed and screened using internal transcribed spacers (ITS) as target DNAs of both pathogens. An ITS-Rs-LAMP assay for R. solani and an ITS-Mp-LAMP assay for M. phaseolina that can detect the pathogen in diseased soybean tissues in the field have been developed. Both LAMP assays efficiently amplified the target genes over 60 min at 62°C. A yellow-green color (visible to the naked eye) or intense green fluorescence (visible under ultraviolet light) was only observed in the presence of R. solani or M. phaseolina after addition of SYBR Green I. The detection limit of the ITS-Rs-LAMP assay was 10 pg μl⁻¹ of genomic DNA; and that of the ITS-Mp-LAMP assay was 100 pg μl⁻¹ of genomic DNA. Using the two assays described here, we successfully and rapidly diagnosed suspect diseased soybean samples collected in the field from Jiangsu and Anhui provinces.

摘要

本文报道了一种直接检测受感染大豆组织中致病真菌的新方法。该方法可快速诊断由立枯丝核菌引起的大豆幼苗猝倒病和由菜豆壳球孢引起的大豆炭腐病,其特点是采用环介导等温扩增技术(LAMP)。以两种病原菌的内部转录间隔区(ITS)作为靶DNA设计并筛选引物。已开发出用于立枯丝核菌的ITS-Rs-LAMP检测法和用于菜豆壳球孢的ITS-Mp-LAMP检测法,可在田间患病大豆组织中检测病原菌。两种LAMP检测法均在62℃下60分钟内有效扩增了靶基因。加入SYBR Green I后,仅在存在立枯丝核菌或菜豆壳球孢的情况下观察到黄绿色(肉眼可见)或强烈绿色荧光(紫外光下可见)。ITS-Rs-LAMP检测法的检测限为10 pg μl⁻¹基因组DNA;ITS-Mp-LAMP检测法的检测限为100 pg μl⁻¹基因组DNA。使用本文所述的两种检测法,我们成功快速地诊断了从江苏和安徽两省田间采集的疑似患病大豆样本。

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