Levofloxacin and sulfamethoxazole induced alterations of biomolecules in Pseudokirchneriella subcapitata

Abstract

Levofloxacin (LEV) and sulfamethoxazole (SMX) are two extensively used antibiotics. Most investigations have been concentrated on the toxic effects of antibiotics on algal species evaluated with traditional ecotoxicological endpoints; however, limited information is available on the alterations in biomolecules induced by antibiotics. Here we investigated alterations in the structure and function of biomolecules to a model species Pseudokirchneriella subcapitata following exposure of LEV and SMX by applying Fourier transform infrared spectroscopy (FTIR). The growth inhibition tests revealed that both LEV and SMX had negative effects on algal growth, while SMX was found to be more toxic to P. subcapitata than LEV. Based on the FTIR analysis, alterations in the structure, composition and function of lipids and proteins were observed on microalgal cells, which were correlated with the dosage of LEV and SMX. As a result of lipid peroxidation induced by LEV and SMX, an increase in the lipid/protein ratio and decrease in the ratios of CH2/lipid, CH3/lipid, carbonyl ester/lipid and olefinic = CH/lipid were observed in all treatment groups with respect to the reference control. Moreover, alterations in the composition and secondary structure of proteins were also observed in accompany with a decrease in the Amide I/Amide II ratio and an increase of the loose β-sheet structure protein. LEV caused an elevated level of lipid peroxidation, while SMX induced a more obvious protein aggregation. The findings from this study showed that FTIR could reveal the toxic mechanism of these two antibiotics to algae at the biochemical level by linking alterations in biomolecules to biochemical dynamics and function.