Department of Plant Pathology and The Key Laboratory of Plant Immunity, Nanjing Agricultural University, Nanjing, Jiangsu 210095, China.
The Key Laboratory of Integrated Management of Crop Diseases and Pests (Ministry of Education), Nanjing, Jiangsu 210095, China.
Plant Dis. 2021 Oct;105(10):2888-2897. doi: 10.1094/PDIS-01-21-0068-RE. Epub 2021 Nov 9.
, , and ' Pythium huanghuaiense' are closely related species and important pathogens of soybean that cause root rot. However, the sequences of commonly used molecular markers, such as rDNA internal transcribed spacer 2 and cytochrome oxidase 1 gene, are similar among these species, making it difficult to design species-specific primers for loop-mediated isothermal amplification (LAMP) assays. The genome sequences of these species are also currently unavailable. Based on a comparative genomic analysis and de novo RNA-sequencing transcript assemblies, we identified and cloned the sequences of the gene, a conserved but highly polymorphic single-copy gene encoding a Puf family RNA-binding protein among oomycetes. After primer design and screening, three LAMP assays were developed that specifically amplified the targeted DNA sequences in . and . at 62°C for 70 min and in ' Pythium huanghuaiense' at 62°C for 60 min. After adding SYBR Green I, a positive yellow-green color (under natural light) or intense green fluorescence (under ultraviolet light) was observed by the naked eye only in the presence of the target species. The minimum concentration of target DNA detected in all three LAMP assays was 100 pg·μl. The assays also successfully detected the target spp. with high accuracy and sensitivity from inoculated soybean seedlings and soils collected from soybean fields. This study provides a method for identification and cloning of candidate detection targets without a reference genome sequence and identified as a novel specific target for molecular detection of three species causing soybean root rot.
卵菌纲的疫霉属、终极腐霉属和腐霉属的种密切相关,是引起大豆根腐病的重要病原菌。然而,这些种常用的分子标记物,如核糖体 DNA 内转录间隔区 2 和细胞色素氧化酶 1 基因的序列在种间非常相似,这使得难以设计用于环介导等温扩增(LAMP)检测的种特异性引物。这些种的基因组序列目前也不可用。基于比较基因组分析和从头 RNA 测序转录组装,我们鉴定并克隆了基因的序列,该基因是编码后生动物 Puf 家族 RNA 结合蛋白的保守但高度多态性的单拷贝基因。在进行引物设计和筛选后,开发了三种 LAMP 检测方法,它们可以在 62°C 下分别特异性扩增目标 DNA 序列,时间分别为 70 分钟(在 和 中)和 60 分钟(在 'Pythium huanghuaiense' 中)。在添加 SYBR Green I 后,只有在存在目标种的情况下,才能通过肉眼观察到阳性的黄绿色(自然光下)或强烈的绿色荧光(紫外线光下)。在所有三种 LAMP 检测方法中,检测到的目标 DNA 的最小浓度均为 100pg·μl。该检测方法还成功地从接种大豆幼苗和从大豆田中采集的土壤中准确和敏感地检测到了目标 种。本研究提供了一种在没有参考基因组序列的情况下鉴定和克隆候选检测靶标的方法,并确定 为分子检测引起大豆根腐病的三种 种的新型特异靶标。