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An In Vivo Fluorescence Image Analysis Tool for Esterase Activity Quantification in Daphnia: Using Calcein AM in Ecotoxicological Studies
Stockholm University, Faculty of Science, Department of Environmental Science. Stockholm University, Science for Life Laboratory (SciLifeLab).ORCID iD: 0009-0000-1027-5938
Stockholm University, Faculty of Science, Department of Environmental Science. Stockholm University, Science for Life Laboratory (SciLifeLab).ORCID iD: 0009-0003-0101-1510
Stockholm University, Science for Life Laboratory (SciLifeLab). Stockholm University, Faculty of Science, Department of Environmental Science.ORCID iD: 0000-0002-6111-7435
Stockholm University, Faculty of Science, Department of Environmental Science.ORCID iD: 0000-0002-4984-8323
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Number of Authors: 52025 (English)In: Environmental Science and Technology, ISSN 0013-936X, E-ISSN 1520-5851, Vol. 59, no 34, p. 18023-18032Article in journal (Refereed) Published
Abstract [en]

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 Daphnia magna. 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 in vivo 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 D. magna, with the added advantage of visualizing intracellular processes in vivo.

Place, publisher, year, edition, pages
2025. Vol. 59, no 34, p. 18023-18032
Keywords [en]
calcein AM, Daphnia, ecotoxicology, fluorescence imaging, high-content screening
National Category
Environmental Sciences
Identifiers
URN: urn:nbn:se:su:diva-247339DOI: 10.1021/acs.est.5c03309ISI: 001555755900001PubMedID: 40841535Scopus ID: 2-s2.0-105015047879OAI: oai:DiVA.org:su-247339DiVA, id: diva2:2000875
Available from: 2025-09-25 Created: 2025-09-25 Last updated: 2025-09-25Bibliographically approved

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Perez-Liñan, AmiraAbele, CedricPierozan, PaulaBreitholtz, MagnusKarlsson, Oskar

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