Tu Yiyi, Wang Yuchun, Jiang Hong, Ren Hengze, Wang Xinchao, Lv Wuyun
College of Tea Science and Tea Culture, Zhejiang A&F University, Hangzhou 311300, China.
Tea Research Institute, Chinese Academy of Agricultural Sciences/National Center for Tea Improvement/Key Laboratory of Biology, Genetics and breeding of Special Economic Animals and Plants, Ministry of Agriculture and Rural Affairs, Hangzhou 310008, China.
J Fungi (Basel). 2024 Jul 3;10(7):467. doi: 10.3390/jof10070467.
Tea leaf spot caused by is an important disease that threatens the healthy growth of tea plants () and results in reductions in the productivity and quality of tea leaves. Early diagnosis of the disease is particularly important for managing the infection. Loop-mediated isothermal amplification (LAMP) assay is an efficient diagnostic technique with the advantages of simplicity, specificity, and sensitivity. In this study, we developed a rapid, visual, and high-sensitivity LAMP assay for detection based on sequence-characterized amplified regions. Two pairs of amplification primers (external primers F3 and B3 and internal primers FIP and BIP) were designed based on a specific sequence in (NCBI accession number: OR987684). Compared to common pathogens of other genera in tea plants and other species in the genus (, , and ), the LAMP method is specific for detecting the species . The assay was able to detect at a minimal concentration of 1 fg/μL genomic DNA at an optimal reaction temperature of 65 °C for 60 min. When healthy leaves were inoculated with in the laboratory, the LAMP method successfully detected in diseased tea leaves at 72 h post inoculation. The LAMP assays were negative when the DNA samples were extracted from healthy leaves. Leaf tissues with necrotic lesions from 18 germplasms of tea plants tested positive for the pathogen by the LAMP assay. In summary, this study established a specific, sensitive, and simple LAMP method to detect , which provides reliable technical support for estimating disease prevalence and facilitates sustainable management of tea leaf spot.
由[病原体名称]引起的茶叶斑病是一种威胁茶树健康生长的重要病害([茶树学名]),会导致茶叶产量和品质下降。该病害的早期诊断对于控制感染尤为重要。环介导等温扩增(LAMP)检测法是一种高效的诊断技术,具有操作简单、特异性强和灵敏度高的优点。在本研究中,我们基于序列特征扩增区域开发了一种快速、可视化且高灵敏度的LAMP检测法用于[病原体名称]的检测。根据[病原体名称]中的一个特定序列(NCBI登录号:OR987684)设计了两对扩增引物(外部引物F3和B3以及内部引物FIP和BIP)。与茶树中其他属的常见病原体以及[病原体所属属名]中的其他物种([物种名称1]、[物种名称2]和[物种名称3])相比,LAMP方法对检测[病原体名称]具有特异性。该检测法在65℃的最佳反应温度下60分钟能够检测到低至1 fg/μL基因组DNA浓度的[病原体名称]。在实验室中,当用[病原体名称]接种健康叶片时,LAMP方法在接种后72小时成功检测到患病茶叶中的[病原体名称]。从健康叶片中提取的DNA样本进行LAMP检测时结果为阴性。通过LAMP检测,对18个茶树种质中带有坏死病斑的叶片组织检测到该病原体呈阳性。总之,本研究建立了一种特异性强、灵敏度高且操作简单的LAMP方法来检测[病原体名称],为评估病害流行情况提供了可靠的技术支持,并有助于茶叶斑病的可持续管理。