Proteomic changes in brain tissues of marine medaka (Oryzias melastigma) after chronic exposure to two antifouling compounds: Butenolide and 4,5-dichloro-2-n-octyl-4-isothiazolin-3-one (DCOIT)
Au, Doris W T
Bajic, Vladimir B.
KAUST DepartmentBioscience Core Lab
Computer, Electrical and Mathematical Sciences and Engineering (CEMSE) Division
Applied Mathematics and Computational Science Program
Computational Bioscience Research Center (CBRC)
Permanent link to this recordhttp://hdl.handle.net/10754/563888
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AbstractSeaNine 211 with active ingredient of 4,5-dichloro-2-n-octyl-4-isothiazolin-3-one (DCOIT) has been used as a "green" antifouling agent worldwide but has raised serious biosafety concerns in coastal environments. DCOIT has the potential to disrupt the neurotransmission in nervous system, but the underlying mechanism has not been clarified. In the present study, we used TMT six-plex labeling coupled with two-dimensional LC-MS/MS analysis to investigate the protein expression profiles in brain tissues of the marine medaka (Oryzias melastigma) after a 28-day exposure to environmentally-realistic concentration of DCOIT at 2.55. μg/L (0.009. μM) or butenolide, one promising antifouling compound, at 2.31. μg/L (0.012. μM). DCOIT and butenolide induced differential expression of 26 and 18 proteins in male brains and of 27 and 23 proteins in female brains, respectively. Distinct mechanisms of toxicity were initiated by DCOIT and butenolide in males, whereas the protein expression profiles were largely similar in females treated by these two compounds. In males, DCOIT exposure mainly led to disruption of mitogen-activated protein kinase (MAPK) signaling pathway, while butenolide affected proteins related to the cytoskeletal disorganization that is considered as a general response to toxicant stress. Furthermore, a sex-dependent protein expression profile was also noted between male and female fish, as evident by the inverse changes in the expressions of common proteins (5 proteins for butenolide- and 2 proteins for DCOIT-exposed fish). Overall, this study provided insight into the molecular mechanisms underlying the toxicity of DCOIT and butenolide. The extremely low concentrations used in this study highlighted the ecological relevance, arguing for thorough assessments of their ecological risks before the commercialization of any new antifouling compound.
SponsorsThis study was supported by grants from China Mineral Resources Research and Development Association (COMR-RDA12SC01) and from the Research Grant Council of HKSAR government (662413), and the King Abdullah University of Science and Technology (SA-C0040/UK-C0016) and the State Key Laboratory in Marine Pollution, City University of Hong Kong. VB was supported by the Base Research Fund from King Abdullah University of Science and Technology.
- Comparative safety of the antifouling compound butenolide and 4,5-dichloro-2-n-octyl-4-isothiazolin-3-one (DCOIT) to the marine medaka (Oryzias melastigma).
- Authors: Chen L, Ye R, Xu Y, Gao Z, Au DW, Qian PY
- Issue date: 2014 Apr
- Hepatic proteomic responses in marine medaka (Oryzias melastigma) chronically exposed to antifouling compound butenolide [5-octylfuran-2(5H)-one] or 4,5-dichloro-2-N-octyl-4-isothiazolin-3-one (DCOIT).
- Authors: Chen L, Sun J, Zhang H, Au DW, Lam PK, Zhang W, Bajic VB, Qiu JW, Qian PY
- Issue date: 2015 Feb 3
- Chronic Exposure of Marine Medaka (Oryzias melastigma) to 4,5-Dichloro-2-n-octyl-4-isothiazolin-3-one (DCOIT) Reveals Its Mechanism of Action in Endocrine Disruption via the Hypothalamus-Pituitary-Gonadal-Liver (HPGL) Axis.
- Authors: Chen L, Zhang W, Ye R, Hu C, Wang Q, Seemann F, Au DW, Zhou B, Giesy JP, Qian PY
- Issue date: 2016 Apr 19
- Degradation kinetics of a potent antifouling agent, butenolide, under various environmental conditions.
- Authors: Chen L, Xu Y, Wang W, Qian PY
- Issue date: 2015 Jan
- Identification of Molecular Targets for 4,5-Dichloro-2-n-octyl-4-isothiazolin-3-one (DCOIT) in Teleosts: New Insight into Mechanism of Toxicity.
- Authors: Chen L, Au DW, Hu C, Peterson DR, Zhou B, Qian PY
- Issue date: 2017 Feb 7