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Combined toxicity of erythromycin and roxithromycin and their removal by Chlorella pyrenoidosa.
Ecotoxicol Environ Saf. 2023 Jun 01; 257:114929.EE

Abstract

The ecological effects of antibiotics in surface water have attracted increasing research attention. In this study, we investigated the combined ecotoxicity of erythromycin (ERY) and roxithromycin (ROX) on the microalgae, Chlorella pyrenoidosa, and the removal of ERY and ROX during the exposure. The calculated 96-h median effect concentration (EC50) values of ERY, ROX, and their mixture (2:1 w/w) were 7.37, 3.54, and 7.91 mg∙L[-1], respectively. However, the predicted EC50 values of ERY+ROX mixture were 5.42 and 1.51 mg∙L[-1], based on the concentration addition and independent action models, respectively. This demonstrated the combined toxicity of ERY+ ROX mixture showed an antagonistic effect on Chlorella pyrenoidosa. During the 14-d culture, low-concentration (EC10) treatments with ERY, ROX, and their mixture caused the growth inhibition rate to decrease during the first 12 d and increase slightly at 14 d. In contrast, high-concentration (EC50) treatments significantly inhibited microalgae growth (p < 0.05). Changes in the total chlorophyll contents, SOD and CAT activities, and MDA contents of microalgae suggested that individual treatments with ERY and ROX induced higher oxidative stress than combined treatments. After the 14-d culture time, residual Ery in low and high concentration Ery treatments were 17.75% and 74.43%, and the residual Rox were 76.54% and 87.99%, but the residuals were 8.03% and 73.53% in ERY+ ROX combined treatment. These indicated that antibiotic removal efficiency was higher in combined treatments than that in individual treatments, especially at low concentrations (EC10). Correlation analysis suggested that there was a significant negative correlation between the antibiotic removal efficiency of C. pyrenoidosa and their SOD activity and MDA content, and the enhanced antibiotic removal ability of microalgae benefited from increased cell growth and chlorophyll content. Findings in this study contribute to predicting ecological risk of coexisting antibiotics in aquatic environment, and to improving biological treatment technology of antibiotics in wastewater.

Authors+Show Affiliations

Co-Innovation Center for Sustainable Forestry in Southern China, College of Biology and the Environment, Nanjing Forestry University, Longpan Road 159, Nanjing 210037, China; National Positioning Observation Station of Hung-tse Lake Wetland Ecosystem in Jiangsu Province, Hongze, Jiangsu 223100, China.Co-Innovation Center for Sustainable Forestry in Southern China, College of Biology and the Environment, Nanjing Forestry University, Longpan Road 159, Nanjing 210037, China; National Positioning Observation Station of Hung-tse Lake Wetland Ecosystem in Jiangsu Province, Hongze, Jiangsu 223100, China.Co-Innovation Center for Sustainable Forestry in Southern China, College of Biology and the Environment, Nanjing Forestry University, Longpan Road 159, Nanjing 210037, China; National Positioning Observation Station of Hung-tse Lake Wetland Ecosystem in Jiangsu Province, Hongze, Jiangsu 223100, China.Co-Innovation Center for Sustainable Forestry in Southern China, College of Biology and the Environment, Nanjing Forestry University, Longpan Road 159, Nanjing 210037, China; National Positioning Observation Station of Hung-tse Lake Wetland Ecosystem in Jiangsu Province, Hongze, Jiangsu 223100, China. Electronic address: uwliwei@163.com.Co-Innovation Center for Sustainable Forestry in Southern China, College of Biology and the Environment, Nanjing Forestry University, Longpan Road 159, Nanjing 210037, China; National Positioning Observation Station of Hung-tse Lake Wetland Ecosystem in Jiangsu Province, Hongze, Jiangsu 223100, China.Co-Innovation Center for Sustainable Forestry in Southern China, College of Biology and the Environment, Nanjing Forestry University, Longpan Road 159, Nanjing 210037, China; National Positioning Observation Station of Hung-tse Lake Wetland Ecosystem in Jiangsu Province, Hongze, Jiangsu 223100, China.

Pub Type(s)

Journal Article

Language

eng

PubMed ID

37084660

Citation

Liu, Kai, et al. "Combined Toxicity of Erythromycin and Roxithromycin and Their Removal By Chlorella Pyrenoidosa." Ecotoxicology and Environmental Safety, vol. 257, 2023, p. 114929.
Liu K, Li J, Zhou Y, et al. Combined toxicity of erythromycin and roxithromycin and their removal by Chlorella pyrenoidosa. Ecotoxicol Environ Saf. 2023;257:114929.
Liu, K., Li, J., Zhou, Y., Li, W., Cheng, H., & Han, J. (2023). Combined toxicity of erythromycin and roxithromycin and their removal by Chlorella pyrenoidosa. Ecotoxicology and Environmental Safety, 257, 114929. https://doi.org/10.1016/j.ecoenv.2023.114929
Liu K, et al. Combined Toxicity of Erythromycin and Roxithromycin and Their Removal By Chlorella Pyrenoidosa. Ecotoxicol Environ Saf. 2023 Jun 1;257:114929. PubMed PMID: 37084660.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Combined toxicity of erythromycin and roxithromycin and their removal by Chlorella pyrenoidosa. AU - Liu,Kai, AU - Li,Jiping, AU - Zhou,Yuhao, AU - Li,Wei, AU - Cheng,Hu, AU - Han,Jiangang, Y1 - 2023/04/20/ PY - 2022/07/20/received PY - 2023/03/12/revised PY - 2023/04/16/accepted PY - 2023/5/8/medline PY - 2023/4/22/pubmed PY - 2023/04/21/entrez KW - Antibiotic removal KW - Biodegradation KW - Macrolide antibiotics KW - Microalgae KW - Toxicity SP - 114929 EP - 114929 JF - Ecotoxicology and environmental safety JO - Ecotoxicol Environ Saf VL - 257 N2 - The ecological effects of antibiotics in surface water have attracted increasing research attention. In this study, we investigated the combined ecotoxicity of erythromycin (ERY) and roxithromycin (ROX) on the microalgae, Chlorella pyrenoidosa, and the removal of ERY and ROX during the exposure. The calculated 96-h median effect concentration (EC50) values of ERY, ROX, and their mixture (2:1 w/w) were 7.37, 3.54, and 7.91 mg∙L[-1], respectively. However, the predicted EC50 values of ERY+ROX mixture were 5.42 and 1.51 mg∙L[-1], based on the concentration addition and independent action models, respectively. This demonstrated the combined toxicity of ERY+ ROX mixture showed an antagonistic effect on Chlorella pyrenoidosa. During the 14-d culture, low-concentration (EC10) treatments with ERY, ROX, and their mixture caused the growth inhibition rate to decrease during the first 12 d and increase slightly at 14 d. In contrast, high-concentration (EC50) treatments significantly inhibited microalgae growth (p < 0.05). Changes in the total chlorophyll contents, SOD and CAT activities, and MDA contents of microalgae suggested that individual treatments with ERY and ROX induced higher oxidative stress than combined treatments. After the 14-d culture time, residual Ery in low and high concentration Ery treatments were 17.75% and 74.43%, and the residual Rox were 76.54% and 87.99%, but the residuals were 8.03% and 73.53% in ERY+ ROX combined treatment. These indicated that antibiotic removal efficiency was higher in combined treatments than that in individual treatments, especially at low concentrations (EC10). Correlation analysis suggested that there was a significant negative correlation between the antibiotic removal efficiency of C. pyrenoidosa and their SOD activity and MDA content, and the enhanced antibiotic removal ability of microalgae benefited from increased cell growth and chlorophyll content. Findings in this study contribute to predicting ecological risk of coexisting antibiotics in aquatic environment, and to improving biological treatment technology of antibiotics in wastewater. SN - 1090-2414 UR - https://www.unboundmedicine.com/medline/citation/37084660/Combined_toxicity_of_erythromycin_and_roxithromycin_and_their_removal_by_Chlorella_pyrenoidosa_ DB - PRIME DP - Unbound Medicine ER -