Toxicity of the cyanobacterial cyclic heptapeptide toxins microcystin-LR and -RR in early life-stages of the African clawed frog (Xenopus laevis)

Citation
Wj. Fischer et Dr. Dietrich, Toxicity of the cyanobacterial cyclic heptapeptide toxins microcystin-LR and -RR in early life-stages of the African clawed frog (Xenopus laevis), AQUAT TOX, 49(3), 2000, pp. 189-198
Citations number
31
Categorie Soggetti
Aquatic Sciences
Journal title
AQUATIC TOXICOLOGY
ISSN journal
0166445X → ACNP
Volume
49
Issue
3
Year of publication
2000
Pages
189 - 198
Database
ISI
SICI code
0166-445X(200006)49:3<189:TOTCCH>2.0.ZU;2-0
Abstract
Numerous cyanobacterial species are capable of producing potent toxins, whi ch have been known to cause intoxications and fatalities in wildlife, lives tock and humans. Microcystis is amongst the most ubiquitously distributed b lue-green algal genus and almost invariably produces cyclic heptapeptide to xins called microcystins (MC). These toxins are highly persistent in water (several weeks). Highest concentrations are found in shallow littoral areas , the primary environment for aquatic early life-stage development. Therefo re, the present study focussed on the potential embryotoxic effects of MC ( MC-LR and -RR) in early life-stages of the amphibian Xenopus laevis. The en dpoints chosen were mortality, malformation and growth inhibition. To achie ve an improved dose-response relationship the uptake of MC was quantified s imultaneously, using a radiolabeled derivative of MC-LR. As one of the best described molecular mechanisms of MC toxicity involves the specific inhibi tion of serine/threonine protein phosphatases-l and -2A (PP), essential enz ymes involved in the mechanisms of cell cycle regulation and maintenance of cellular morphology, the inhibition of PP in X. laevis exposed to MC was m onitored. For this the presence of both PP-I and PP-2A was confirmed by mea ns of SDS-PAGE and immunoblotting. Second, the capacity of MC to inhibit X. laevis embryo-larval PP was corroborated by in vitro incubation of embryo- larval homogenates with MC-LR and -RR and subsequent determination of PP-in hibition. No increased mortality, malformation; or growth inhibition was ob served even at the highest MC concentrations employed. MC had neither a dem onstrable inhibitory effect on X. laevis PP-activity in vivo in the first 9 6 h of exposure. However, as of 96 and 120 h exposure a significant inhibit ion of PP activity was observed at the highest dose (2000 mu g/l) in MC-LR and MC-RR exposed embryo-larvae, respectively. By the same token, no notabl e amounts of radiolabeled [H-3]-MC-LR were taken up during the first 96 h, whereas a drastic increase in [H-3]-MC-LR was observed after feeding of the larvae had commenced. The [H-3]-MC-LR concentration was consistently found to be highest in the viscerothoracal sections of the larvae (2112 +/- 429 mu g MC/kg dry weight after 120 h). The present findings indicate that tran schorional/transdermal absorption of MC in X. laevis is minimal or absent a nd that oral uptake of MC with ambient water is necessary for the developme nt of MC related toxicity. Furthermore, the comparison of the MC doses used in this study with the concentrations reported in surface waters indicate that early life-stages of amphibians (up to 5 days of development) are unli kely to be affected by cyanobacterial blooms producing MC-LR and -RR. (C) 2 000 Elsevier Science B.V. All rights reserved.