Effects of selected metal oxide nanoparticles on multiple biomarkers in Carassius auratus.

OBJECTIVE: To study the biological effects of nanoscale copper oxide (nCuO), zinc oxide (nZnO), cerium dioxide (nCeO2) and their mixtures on Carassius auratus. METHODS: Juvenile fish (Carassius auratus) were exposed to aqueous suspensions of nCuO, nZnO, and nCeO2 (alone and in mixtures) at concentrations of 20, 40, 80, 160, and 320 mg/L. The biomarkers-acetylcholinesterase (AChE) in brain, sodium/potassium-activated ATPase (Na+/K+-ATPase) in gill, and superoxide dismutase (SOD) and catalase (CAT) in liver-were determined after 4 days of exposure. Integrated biomarker response (IBR) was calculated by combining multiple biomarkers into a single value. RESULTS: AChE and SOD activities were significantly inhibited by all test metal oxide nanoparticles (NPs) at high concentrations (⋝160 mg/L) with the exception of nCeO2. Na+/K+-ATPase induction exhibited bell-shaped concentration-response curves. CAT activity was significantly inhibited at concentrations equal to or higher than 160 mg/L. The order of IBR values was nCeO2 ≈ nZnO/nCeO2 ≈ nCuO/nCeO2 < nCuO/nZnO/nCeO2 < nZnO < nCuO < nCuO/nZnO. The joint effect seemed to be synergistic for nCuO/nZnO mixtures, additive for the ternary mixture and less than additive or antagonistic for the binary mixtures containing nCeO2. CONCLUSION: Concentration-dependent changes of enzymatic activities (AChE, Na+/K+-ATPase, SOD, and CAT) were observed in fish exposed to nanoscale metal oxides. IBR analysis allowed good discrimination between the different exposures and might be a useful tool for the quantification of integrated negative effects induced by NPs toward fish.

[Community Structure and Microbial Function Responses of Biofilms Colonizing on Microplastics with Vertical Distribution in Urban Water].

Microplastics have received increasing attention worldwide due to their carrier effects. In the aquatic environment, microplastics always show a vertical distribution, which thereby may change the structure and function of the attached microbial communities. However, few studies have focused on this alteration. In this study, the structural changes and functional expression responses of the attached bacterial communities to microplastics under vertical distribution were investigated in the field combined with high-throughput sequencing technology. Polyethylene terephthalate (PET) and polyvinyl chloride (PVC) were selected as the target microplastics, which were frequently detected in the aqueous environment. The results showed that the α-diversity of bacterial communities attached to PET microplastics was much higher than that of those attached to PVC microplastics. The abundance and diversity of the bacterial communities attached to PET and PVC both increased with the increase in water depth. The α-diversity index of bacteria attached to the two typical microplastics was significantly higher in deep water (90 cm) than that in water 30 cm and 60 cm deep. The Cyanobacteria, Proteobacteria, Planctomycetes, and Verrucomicrobia were the dominant phyla in the attached bacterial communities. In addition, the deep water distinctly altered the bacteria community attached to different microplastics. The results of functional prediction showed that the functional expression of pyrimidine metabolism, amino sugar and nucleotide sugar metabolism, starch and sucrose metabolism, and aminoacyl-tRNA biosynthesis were positively correlated with water depth. In addition, the functional responses of the bacterial communities attached to microplastics were also increased, especially in deep water. Further, the bacterial functions of those attached to PET were significantly higher than that of those attached to PVC. This suggests that both the microplastic polymer and the water depth could affect the structure and function of the attached bacterial communities and that the water depth was more important, which may be related to the difference in the vertical distribution of light and turbidity. The results of this study provide a new insight into the microbial response to and environmental risk of microplastic pollution.