Perez-Liñan Amira, Abele Cedric, Pierozan Paula, Breitholtz Magnus, Karlsson Oskar
Science of Life Laboratory, Department of Environmental Science, Stockholm University, 114 18 Stockholm, Sweden.
Department of Environmental Science, Stockholm University, 114 18 Stockholm, Sweden.
Environ Sci Technol. 2025 Sep 2;59(34):18023-18032. doi: 10.1021/acs.est.5c03309. Epub 2025 Aug 21.
There is an increasing need for new approach methodologies (NAMs) to generate relevant ecotoxicological data. This study demonstrates the strengths of calcein AM, a highly sensitive fluorescent stain for esterase activity, in an automated image-based multiwell plate assay for detecting sublethal effects in . Sample processing and feeding conditions were optimized to ensure a uniform dye distribution. The protocol was validated using two esterase inhibitors, triphenyl phosphate and netilmicin sulfate, and subsequently applied to test the environmental contaminants methoxychlor, lindane, tributyltin chloride, pentachlorophenol, diuron, and ethofumesate. The test organisms were imaged using automated confocal microscopy, and fluorescence intensity was quantified to generate concentration-response curves. The effects of triphenyl phosphate and netilmicin sulfate were observed at concentrations 3-fold and 6-fold lower, respectively, than in the OECD 202 immobilization test. All tested contaminants also inhibited esterase activity, with concentrations resulting in no esterase activity at 48 h, correlating with mortality observed at 48 h. This method provides a new sensitive fluorescent tool for detecting sublethal chemical effects in , with the added advantage of visualizing intracellular processes .
越来越需要新的方法学(NAMs)来生成相关的生态毒理学数据。本研究证明了钙黄绿素乙酰甲酯(一种对酯酶活性高度敏感的荧光染料)在基于图像的自动化多孔板测定中检测[具体受试生物]亚致死效应的优势。优化了样品处理和喂食条件以确保染料均匀分布。使用两种酯酶抑制剂磷酸三苯酯和硫酸奈替米星对该方案进行了验证,随后将其应用于测试环境污染物甲氧滴滴涕、林丹、三丁基氯化锡、五氯苯酚、敌草隆和乙氧呋草黄。使用自动共聚焦显微镜对受试生物进行成像,并对荧光强度进行定量以生成浓度-反应曲线。观察到磷酸三苯酯和硫酸奈替米星的效应分别比经合组织202号固定化试验中的浓度低3倍和6倍。所有测试的污染物也都抑制了酯酶活性,在48小时导致无酯酶活性的浓度与48小时观察到的死亡率相关。该方法为检测[具体受试生物]中的亚致死化学效应提供了一种新的灵敏荧光工具,还具有可视化细胞内过程的额外优势。