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Updated: May 15, 2025

Zebrafish as a Model to Assess the Teratogenic Potential of Nitrite
Published on: February 16, 2016
Zebrafish embryos ecotoxicity traceability of pharmaceutical wastewater during simultaneous
Shuyan Chen1, Linya Yi1, Yuancai Chen1
1Ministry of Education Key Laboratory of Pollution Control and Ecological Remediation for Industrial Agglomeration Area, School of Environment and Energy, South China University of Technology, Guangzhou 510006, China.
None:
Toxicity assessments based on transcriptomics and metabolomics at target organs are magnitude difference due to the tremendous variations in the sensitivity of receptor binding sites (subunits), which often require expensive instrumentation using quantitative whole-body autoradiography. In this study, zebrafish embryos combined with toxicity identification evaluation (TIE) and ECOSAR toxicity prediction were applied to monitor comprehensive toxicity changes of fermentation pharmaceutical wastewater (FPW) in the expanded granular sludge bed (EGSB) and the modified simultaneous nitrification-denitrification (SND) process. FPW with high toxicity (30.93 TU) was predominately detoxified (to 4.04 TU) in anaerobic EGSB process, in which chlortetracycline (CTC) was degraded via demethylation, dechlorination and ring-cleaving. TIE results showed that non-polar pollutants contributed to the major toxicity and existed in the whole process. The pH adjustment significantly influenced the toxicities of CTC and its mixture with NH4+-N (MCTC+NH4+) or NO2--N (MCTC+NO2-) due to the hydrolysis and chelation. Noticeably, nearly no nitrite/nitrate were accumulated in SND treatment process, which greatly alleviated the toxicities of MCTC+NH4+ and MCTC+NO2- due to no generation of free ammonia and free nitrous acid. MCTC+NH4+ exhibited antagonistic toxicity in all test pH, but MCTC+NO2- converted from synergistic (pH i) to antagonistic (pH 7.5). This study deepened the detoxification mechanistic interpretations of FPW in the modified EGSB-SND process as well as related toxicity variation information.

