Zhang Ting, Xu Han, Liu Mengdi, Zhang Wei
Institute of Plant Inspection and Quarantine, Chinese Academy of Inspection and Quarantine, Beijing, China.
Marine College, Shandong University, Weihai, China.
Front Plant Sci. 2025 Jan 20;15:1502052. doi: 10.3389/fpls.2024.1502052. eCollection 2024.
Noxious plants pose a significant threat to human and livestock health, as well as to the safety of agricultural and forestry ecosystems. Accurate and rapid identification of these plants is crucial for risk prevention. This paper explores for the first time the development and application of a rapid detection technology for noxious plants based on a novel isothermal amplification technique. We targeted the seeds, leaves, and grain impurities of four major noxious weeds: , the complex, , and , we designed and screened primers and probes suitable for this isothermal amplification method, determined their limit of detection, optimized the genomic DNA extraction methods, and verified the method. We developed genomic DNA extraction methods for single tissue components of plant seeds and leaves, as well as for mixed tissue components. Ultimately, we established standardized detection protocols for different tissue forms of each species, significantly enhancing detection efficiency. This study enables the detection positive samples in seeds or leaves within 10 to 15 minutes and positive samples from mixtures within 12 to 18 minutes. The entire process, from sample collection, genomic DNA preparation to reaction completion, takes approximately 35 minutes. This detection technology, which marks the first development of an isothermal amplification-based method for noxious plants, meets the needs for on-site rapid testing, aiding in the timely identification of risks and the implementation of corresponding prevention and control measures.
有毒植物对人类和牲畜健康以及农业和林业生态系统安全构成重大威胁。准确、快速地识别这些植物对于风险预防至关重要。本文首次探索了基于一种新型等温扩增技术的有毒植物快速检测技术的开发与应用。我们针对四种主要有害杂草的种子、叶片和谷粒杂质,即 、 复合体、 和 ,设计并筛选了适用于这种等温扩增方法的引物和探针,确定了它们的检测限,优化了基因组DNA提取方法,并对该方法进行了验证。我们开发了针对植物种子和叶片单一组织成分以及混合组织成分的基因组DNA提取方法。最终,我们为每个物种的不同组织形式建立了标准化检测方案,显著提高了检测效率。本研究能够在10至15分钟内检测出种子或叶片中的阳性样本,在12至18分钟内检测出混合物中的阳性样本。从样本采集、基因组DNA制备到反应完成的整个过程大约需要35分钟。这种检测技术标志着首次开发出基于等温扩增的有毒植物检测方法,满足了现场快速检测的需求,有助于及时识别风险并实施相应的预防和控制措施。