Antibiotics can cause severe ecological problems for aquatic ecosystems due to their wide use and incomplete removal. Microcystis aeruginosa was exposed to different levels of erythromycin (ERY) and sulfamethoxazole (SMX) separately to assess their cytotoxic effects on harmful cyanobacteria. The production and release of the toxin MC-LR was measured, and several endpoints were investigated using flow cytometry (FCM) for 7 d. ERY resulted in cell membrane hyperpolarization and a hormesis effect on growth rate and chlorophyll a fluorescence at environmentally relevant concentrations (0.5 and 5 μg/L). Microcystis exhibited elevated photosynthesis and hyperpolarization at 50 and 125 μg/L of SMX. An increase of metabolically non-active cells was observed in either ERY or SMX cultures while stimulation of esterase activity was also found at 7 d. ERY and SMX caused damage of membrane integrity due to the overproduction of ROS, which led to increased release of MC-LR. MC-LR production apparently was induced by ERY (0.5-500 μg/L) and SMX (50 and 125 μg/L). In conclusion, ERY and SMX can disrupt the physiological status of Microcystis cells and stimulate the production and release of MC-LR, which can exacerbate potential risks to water systems.
Keywords: Antibiotics toxicity; Cell membrane properties; Flow cytometry; Microcystins; Microcystis aeruginosa.
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