4.7 Article

Assessment of toxic mechanisms and mode of action to three different levels of species for 14 antibiotics based on interspecies correlation, excess toxicity, and QSAR

Journal

CHEMOSPHERE
Volume 317, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2023.137795

Keywords

Antibiotics; Daphnia magna; Pseudokirchneriella subcapitata; Vibrio fischeri; Excess toxicity; Mode of action

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In this study, the mode of action (MOA) of antibiotics against nontarget organisms was investigated using 14 antibiotics and three different species. The results showed that there were poor interspecies toxicity correlations and that antibiotics exhibited excess toxicity to algae and Daphnia magna but not to Vibrio fischeri. Molecular docking simulations and QSAR models revealed that the interactions between antibiotics and target receptors played key roles in their toxicity. These results provide valuable insights into the toxic mechanisms and MOA of antibiotics in different species.
Antibiotics have received much attention owing to their ecotoxicity toward nontarget aquatic creatures. How-ever, the mode of action (MOA) of toxicity against nontarget organisms is unclear in some aquatic organisms. In this study, the comparison of toxicities through interspecies correlations, excess toxicity calculated from toxicity ratio, and quantitative structure-activity relationship (QSAR) was carried out to investigate the MOAs for 14 antibiotics among Daphnia magna, Vibrio fischeri, and Pseudokirchneriella subcapitata. The results showed that interspecies toxicity correlations were very poor between any two of the three species for the 14 antibiotics. The toxicity ratio revealed that most antibiotics exhibited excess toxicity to algae and Daphnia magna but not to V. fischeri, demonstrating that some antibiotics share the same MOA, but some antibiotics share different MOAs among the three different levels of species. P. subcapitata was the most sensitive species, and V. fischeri was the least sensitive species. This is because of the differences in the biouptake and interactions of antibiotics with the target receptors between the three different trophic levels of the species. Molecular docking simulations sug-gested that the toxicity of antibiotics depends highly on their interactions with target receptors through hydrogen bonds, electrostatic or polar interactions, pi bond interactions, and van der Waals forces. QSAR models demon-strated that hydrogen bonding and electrophilicity/nucleophilicity play key roles in the interaction of antibiotics with different receptors in the three species. The toxic mechanisms of antibiotics are attributed to the interactions between electrophilic antibiotics and biological nucleophiles, and hydrogen-bond interactions. These results are valuable for understanding the toxic mechanisms and MOA of the three different levels of species.

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