ZFIN ID: ZDB-PUB-170911-3
Imazalil exposure induces gut microbiota dysbiosis and hepatic metabolism disorder in zebrafish
Jin, C., Luo, T., Zhu, Z., Pan, Z., Yang, J., Wang, W., Fu, Z., Jin, Y.
Date: 2017
Source: Comparative biochemistry and physiology. Toxicology & pharmacology : CBP   202: 85-93 (Journal)
Registered Authors: Luo, Ting
Keywords: Gut microbiota, Imazalil, Metabolism, Zebrafish
MeSH Terms:
  • Animals
  • Chemical and Drug Induced Liver Injury/pathology*
  • Dose-Response Relationship, Drug
  • Fungicides, Industrial/toxicity*
  • Gastrointestinal Microbiome/drug effects*
  • Imidazoles/administration & dosage
  • Imidazoles/toxicity*
  • Liver/metabolism*
  • Male
  • Water Pollutants, Chemical/toxicity
  • Zebrafish
PubMed: 28888875 Full text @ Comp. Biochem. Physiol. C Toxicol. Pharmacol.
ABSTRACT
The fungicide imazalil (IMZ) is used extensively to preserve freshness, prevent decay and control fungal infections in fruits, vegetables or other plants. Recently, some studies have reported that the real in aquatic systems have reached very high levels. Here, male adult zebrafish were exposed to 100 and 1000μg/L IMZ for 1, 7, 21days, and the gut microbiota and hepatic metabolism were evaluated. Exposure to a high concentration of IMZ for 21days decreased mucin secretion in the gut. Sequencing of the V3-V4 region of the bacterial 16S rRNA gene revealed a significant increase in the diversity of gut microbiota in male zebrafish. At the phylum level, the composition of Proteobacteria and Bacteroidetes was decreased, while those Fusobacteria and Firmicutes increased in the gut after exposure to 1000μg/L IMZ for 21days. At the genus level, 29 species of microorganisms were significantly changed after IMZ exposure. Based on GC/MS metabolomics analysis, 101 metabolites were observably significantly altered in the 1000μg/L IMZ-treatment group. These changed metabolites were mainly associated with the pathway of glycolysis, amino acid metabolism, and lipid metabolism. In addition, the transcription of some genes related to glycolysis and lipid metabolism, including Aco, Cpt1, Acc1, Srebp1a and Fas, was decreased significantly in the liver of zebrafish when exposed to 100 and 1000μg/L IMZ for 7 or 21days. These results indicated that exposure to IMZ could cause gut microbiota dysbiosis and metabolic disorders in adult zebrafish.
ADDITIONAL INFORMATION