TABLE 6.
Studies linking exposure to polybrominated diphenyl ethers and microbiota changes.
References | Animal model | PBDE dose | Microbiota changes | Health effects |
Studies in animals | ||||
Chen et al. (2018b) | Zebrafish | PBDE mixture (DE-71) (5 ng/L) | • Higher relative abundance of Firmicutes and Bacteroidetes in the gut of male fish, but a lower Firmicutes/Bacteroidetes ratio was observed. • DE-71 led to decreased Bacteroidetes in the gut of female fish with a higher Firmicutes/Bacteroidetes ratio. • Mycoplasma, Ruminiclostridium, unclassified Firmicutes sensu stricto and Fusobacterium were not detected in the gut of male and female fish. |
• In males, an alteration in intestinal health was observed due to exposure to DE-71, which led to disruptions of the neural signaling, of the integrity of the epithelial barrier, inflammatory response, oxidative stress and antioxidant capacity, as well as disruptions of the detoxifying capacity. • In females, the physiological activities of the intestine remained unchanged. |
Wang et al. (2018) | Mice | PBDE-47 (0, 0.002 and 0.2 mg/kg) | • Exposure resulted in decreased abundance of Bacteroidetes and Proteobacteria and in an increase of Actinobacteria at the phylum level. • Exposure resulted in increased abundance of Candidatus_Saccharimonas, Ruminococcaceae_UCG-013, Staphylococcus, Gemella, Eubacterium_nodatum_group, Corynebacterium_1 and Paenalcaligenesen and in a decrease in the abundance of Turicibacter and Anaerotruncus at the genus level. |
• High fat diet-induced obesity increased as a result of the exposure to BDE-47. • Steatosis of the liver, disturbances in glucose homeostasis, metabolic dysfunction, and altered levels of gene mRNAs involved in lipid metabolism were found in mice fed high-fat diet and exposed BDE-47. |
Li et al. (2017) | Male C57BL/6 mice | PBDE-47 (10–100 μmol/kg) and PBDE-99 (10–100 μmol/kg) | _ | • Absence of gut microbiome increased PBDE-99-mediated upregulation of many genes involved in drug metabolism and it also affected hydroxylation of PBDEs. • Exposure to PBDE increased unconjugated bile acids in multiple bio-compartments in a gut microbiota-dependent manner. |
Studies in humans | ||||
Laue et al. (2019) | Children | PBDE-47, PBDE-99, PBDE-100, PBDE-153 (environmental exposure) | • Exposure to PBDE-99 was associated with a decrease in uncultured bacteria within the Ruminococcaceae NK4A214 group and exposure to PBDE-47 led to differences in Ruminococcus 2. | _ |
PBDEs: Polybrominated diphenyl ethers; DE-71: PBDE mixture; PBDE-47: 2, 2′, 4, 4′-tetrabromodiphenil ether; PBDE-99: 2, 2′, 4, 4′, 5-pentabromodiphenil ether; PBDE-100: 2,2′,4,4′,6-pentabromodiphenyl ether; PBDE-153: 2,2′,4,4′,5,5′-Hexabromodiphenyl ether.