Key Laboratory of Marine Environment and Ecology, College of Environmental Science and Engineering, Ocean University of China, Ministry of Education, Qingdao, 266100, China.
Laboratory for Marine Ecology and Environmental Science, Pilot National Laboratory for Marine Science and Technology (Qingdao), Qingdao, 266237, China.
Mar Biotechnol (NY). 2024 Jun;26(3):475-487. doi: 10.1007/s10126-024-10310-2. Epub 2024 Apr 11.
Prorocentrum lima, a widely distributed dinoflagellate known for its production of harmful biotoxins, poses a significant threat to humans, aquaculture, and marine ecosystems. As a result, the detection of this toxic alga in coastal waters has become an urgent research focus. In this study, a rapid, sensitive, and cost-effective detection method based on loop-mediated isothermal amplification (LAMP) was developed to identify P. lima. In this method, cell extracts of P. lima were diluted and used directly as templates for amplification, eliminating the need for nucleic acid purification and simplifying the detection process. Hydroxy naphthol blue (HNB) was incorporated into the reaction mix to facilitate result interpretation, enabling visual determination of the amplification outcome with the naked eye. The entire detection process, from DNA extraction to template amplification and product detection, could be completed within 80 min using a simple constant temperature-control device. This LAMP-based detection method demonstrated excellent reliability, specificity, and a low detection limit of 5.87 cells/mL for DNA crude extract. The assay offered an efficient alternative to PCR for rapid detection of P. lima. By streamlining the detection process and offering a visual readout, this technique holds promise for efficient and routine monitoring of harmful algal species, benefitting both research efforts and environmental management strategies.
利马原甲藻是一种分布广泛的甲藻,其产生的有害生物毒素对人类、水产养殖和海洋生态系统构成了重大威胁。因此,检测近岸水域中的这种有毒藻类已成为当务之急。本研究建立了一种快速、灵敏、经济的基于环介导等温扩增(LAMP)的利马原甲藻检测方法。该方法以利马原甲藻细胞提取物为模板进行扩增,无需核酸提取,简化了检测过程。在反应体系中加入羟萘蓝(HNB),便于结果判读,可通过肉眼直接观察判断扩增结果。采用简单的恒温水浴设备,从 DNA 提取到模板扩增和产物检测,整个检测过程可在 80 min 内完成。该 LAMP 检测方法具有良好的可靠性、特异性,对 DNA 粗提物的检测限低至 5.87 个细胞/mL。与 PCR 相比,该方法具有快速检测利马原甲藻的优势。该技术简化了检测过程并提供了可视化结果,有望用于有害藻类的高效常规监测,有益于研究工作和环境管理策略。