Liu Fuguo, Zhang Chunyun, Li Jiahao, Ma Jinju, Duan Yu, Wang Yuanyuan, Chen Guofu
School of Marine Science and Technology, Harbin Institute of Technology (Weihai), Wenhua West Road, 2#, Weihai, 264209, People's Republic of China.
Jia Sixie College of Agriculture, Weifang University of Science and Technology, Weifang, 262700, People's Republic of China.
Mar Biotechnol (NY). 2025 Jan 13;27(1):28. doi: 10.1007/s10126-024-10407-8.
Recently, the scale and frequency of harmful algae blooms (HABs) have gradually increased, posing a serious threat to human health, marine ecosystems and economic development. For early warning, a method is required that can quickly detect and monitor microalgae. It is proposed to use aptamer targeted to Prorocentrum minimum, along with exonuclease III (Exo III), gold nanoparticles, target single-stranded DNA and hairpin structure probe to construct a new method, i.e. aptamer-lateral flow dipstick (LFD) based on Exo III-assisted signal amplification assay (ALBEA). The key conditions, including signal amplification and LFD detection, are optimized. Under the optimal conditions, the detection limit of ALBEA was 1.25 cells mL. The cross-reactivity test showed no positive result except for P. minimum, indicating that the method is highly specific. The anti-interference test confirmed that the technique was not affected by the presence of other microalgae. The tested results of P. minimum cultured under different nutrient conditions and different growth stages demonstrated that the method is not affected by the cell state. Furthermore, the test results of simulated natural water samples further validated the practicality of the ALBEA. In conclusion, the established ALBEA offers a sensitive, specific and user-friendly tool, which can be used for the rapid detection of P. minimum and also provides a reference for the detection of other microalgae.
近年来,有害藻华(HABs)的规模和频率逐渐增加,对人类健康、海洋生态系统和经济发展构成严重威胁。为了进行预警,需要一种能够快速检测和监测微藻的方法。本文提出利用针对微小原甲藻的适配体,结合核酸外切酶III(Exo III)、金纳米颗粒、靶标单链DNA和发夹结构探针构建一种新方法,即基于Exo III辅助信号放大分析(ALBEA)的适配体侧流试纸条(LFD)。对包括信号放大和LFD检测在内的关键条件进行了优化。在最佳条件下,ALBEA的检测限为1.25个细胞/毫升。交叉反应试验表明,除微小原甲藻外无阳性结果,表明该方法具有高度特异性。抗干扰试验证实该技术不受其他微藻存在的影响。对不同营养条件和不同生长阶段培养的微小原甲藻的测试结果表明,该方法不受细胞状态的影响。此外,模拟天然水样的测试结果进一步验证了ALBEA的实用性。总之,所建立的ALBEA提供了一种灵敏、特异且用户友好的工具,可用于快速检测微小原甲藻,也为其他微藻的检测提供了参考。