PUBLICATION
BDE-209-induced genotoxicity, intestinal damage and intestinal microbiota dysbiosis in zebrafish (Danio Rerio)
- Authors
- Wang, J., Liu, C., Wang, S.P., Zhang, T.X., Chen, J.Y., Zhou, Q., Hou, Y., Yan, Z.G.
- ID
- ZDB-PUB-230914-54
- Date
- 2023
- Source
- The Science of the total environment 905: 167009 (Journal)
- Registered Authors
- Wang, Jing
- Keywords
- BDE-209, Genotoxicity, Intestinal damage, Intestinal microbiota
- MeSH Terms
-
- Adult
- Animals
- Dysbiosis/chemically induced
- Flame Retardants*/metabolism
- Flame Retardants*/toxicity
- Gastrointestinal Microbiome*
- Halogenated Diphenyl Ethers/metabolism
- Humans
- Lipid Metabolism Disorders*
- Male
- RNA, Ribosomal, 16S
- Steroids/metabolism
- Zebrafish/metabolism
- PubMed
- 37704147 Full text @ Sci. Total Environ.
Citation
Wang, J., Liu, C., Wang, S.P., Zhang, T.X., Chen, J.Y., Zhou, Q., Hou, Y., Yan, Z.G. (2023) BDE-209-induced genotoxicity, intestinal damage and intestinal microbiota dysbiosis in zebrafish (Danio Rerio). The Science of the total environment. 905:167009.
Abstract
The environmental presence of polybrominated diphenyl ethers (PBDEs) is ubiquitous due to their wide use as brominated flame retardants in industrial products. As a common congener of PBDEs, decabromodiphenyl ether (BDE-209) can pose a health risk to animals as well as humans. However, to date, few studies have explored BDE-209's toxic effects on the intestinal tract, and its relevant mechanism of toxicity has not been elucidated. In this study, adult male zebrafish were exposed to BDE-209 at 6 μg/L, 60 μg/L and 600 μg/L for 28 days, and intestinal tissue and microbial samples were collected for analysis to reveal the underlying toxic mechanisms. Transcriptome sequencing results demonstrated a dose-dependent pattern of substantial gene differential expression in the group exposed to BDE-209, and the differentially expressed genes were mainly concentrated in pathways related to protein synthesis and processing, redox reaction, and steroid and lipid metabolism. In addition, BDE-209 exposure caused damage to intestinal structure and barrier function, and promoted intestinal oxidative stress, inflammatory response, apoptosis and steroid and lipid metabolism disorders. Mechanistically, BDE-209 induced intestinal inflammation by increasing the levels of TNF-α and IL-1β and activating the NFκB signaling pathway, and might induce apoptosis through the p53-Bax/Bcl2-Caspase3 pathway. BDE-209 also significantly inhibited the gene expression of rate-limiting enzymes such as Sqle and 3βhsd (p < 0.05) to inhibit cholesterol synthesis. In addition, BDE-209 induced lipid metabolism disorders through the mTOR/PPARγ/RXRα pathway. 16S rRNA sequencing results showed that BDE-209 stress reduced the richness and diversity of intestinal microbiota, and reduced the abundance of probiotics (e.g., Bifidobacterium and Faecalibacterium). Overall, the results of this study help to clarify the intestinal response mechanism of BDE-209 exposure, and provide a basis for evaluating the health risks of BDE-209 in animals.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping