Open AccessFlow cytometric analysis of chronic and acute toxicity of copper(II) on the marine dinoflagellate Amphidinium carterae
Author(s) -
Lage Olga M.,
Sansonetty Filipe,
O'Connor JoséEnrique,
Parente Ana M.
Publication year - 2001
Publication title -
cytometry
Language(s) - English
Resource type - Journals
eISSN - 1097-0320
pISSN - 0196-4763
DOI - 10.1002/1097-0320(20010701)44:3<226::aid-cyto1115>3.0.co;2-9
Subject(s) - copper , flow cytometry , toxicity , toxicant , biology , copper toxicity , bioaccumulation , intracellular , autofluorescence , oxidative stress , chemistry , biophysics , biochemistry , fluorescence , microbiology and biotechnology , environmental chemistry , physics , organic chemistry , quantum mechanics
Abstract Background Copper(II) is a heavy metal whose levels have increased in some marine ecosystems to polluting levels. Dinoflagellates, an important phytoplankton group, are at the base of aquatic food chains and bioaccumulation of copper by these microorganisms can result in complex ecosystem alterations, so we investigated how copper disturbs those cells. Methods Cytotoxic effects of sublethal and lethal copper concentrations ranging from 4.2 nM (control condition) to 3.13 μM estimated labile copper were studied in batch cultures of Amphidinium carterae . Cell morphology, motility, autofluorescence, and fluorescein diacetate (FDA)–dependent fluorescence generation were evaluated by flow cytometry (FCM) and microscopy. Results Exposure of A. carterae to toxic levels of copper impaired cell mobility, delayed cell proliferation, led to increased green autofluorescence, and at 3.13 μM labile copper also induced encystment and death. Chlorophyll fluorescence, however, was not affected. Kinetic FCM assay of FDA‐dependent fluorescence generation showed a dose‐dependent enhancement of fluorescein fluorescence immediately after copper addition and in cultures with sustained exposure to this toxicant. Conclusions Our data suggest that copper toxicity occurs quickly at the membrane level in relation to oxidative stress generation. Based on fluorescence kinetic studies, the Na + /H + antiporter seemed to be affected by copper, thereby affecting intracellular pH. Cytometry 44:226–235, 2001. © 2001 Wiley‐Liss, Inc.