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ABSTRACT Mussels (Mytilus spp.) are used frequently in biological effects studies and biomonitoring programs either as transplanted groups or native populations. However, as a result of the similarities in the [...]

Early molecular events with correlation to disease, such as aberrant DNA methylation, emphasize the importance of DNA methylation as a potential environmental biomarker. Currently, little is known regarding how various environmental contaminants and mixtures alter DNA methylation in aquatic organisms, and testing is both time- and labor-consuming. Therefore, the potential of an in vitro screening method was evaluated by exposing zebrafish liver cells (ZF-L) for 96 h to the nonmutagenic model substance 5′-azacytidine (AZA), as well as a selection of environmental pollutants such as sodium arsenite (NAS), 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), 17α-ethinylestradiol (EE2), and diethylstilbestrol (DES). Six single genes with reported and anticipated importance in cancer were selected for analysis. Methylation of gene promoter areas was monitored by bisulfite conversion and high-resolution melt (HRM) analysis after exposure to sublethal concentrations of the test compounds. Subsequently, results were validated with direct bisulfite sequencing. Exposure of ZF-L cells to 0.5 μMAZA for 96 h led to hypomethylation of genes with both low and high basal methylation indicating similarity to mechanism of action in mammals. Further, NAS, EE2, and DES were shown to induce significant alterations in methylation, whereas TCDD did not. It was concluded that cell line exposure in combination with HRM may provide an initial contaminant screening assay by quantifying DNA methylation alterations with high throughput capacity. In addition, the rapid determination of effects following contaminant exposure with this in vitro system points to the possibility for new in vivo applications to be useful for environmental monitoring. [ABSTRACT FROM PUBLISHER]

The purpose of this study was to investigate the cytotoxicity and oxidative stress responses of selected engineered carbon and titanium dioxide (TiO2) nanomaterials to rainbow trout (Oncorhynchus mykiss) primary hepatocytes. The engineered nanomaterials tested were C60 fullerenes, multiwall nanotubes (MWNT), single-wall nanotubes (SWNT) (functionalized and nonfunctionalized), and TiO2 of 5 and 200 nm in size. Characterization of these materials showed that they were typically present in solution as agglomerates. The engineered nanoparticle agglomerates were cytotoxic at nominal concentrations of >3 mg/L, and certain MWNT and SWNT produced significant intracellular reactive oxygen species (ROS) production as well as cytotoxicity. Analyses of the MWNT responsible for ROS production and cytotoxicity for selected transition metals demonstrated the presence of residual cobalt (Co), which was not present in the nonreactive/non-bioactive MWNT. Cobalt alone was not able to induce the observed effects in hepatocyte cells; however, coexposure with MWNT resulted in an increase in cytotoxicity. Data suggest that trace metals often associated with commercial nanotubes are responsible for the observed biological effects. In addition, other mechanisms, such as the proposed facilitated transport (e.g., Trojan horse) type mechanism of uptake, may provoke an increased response compared to aqueous exposures of trace metals in the absence of carbon nanoparticles. [ABSTRACT FROM AUTHOR]

The Norwegian water column monitoring program investigates the biological effects of offshore oil and gas activities in Norwegian waters. In three separate surveys in 2006, 2008, and 2009, bioaccumulation and biomarker responses were measured in mussels (Mytilus edulis) and Atlantic cod (Gadus morhua) held in cages at known distances from the produced water (PW) discharge at the Ekofisk oil field. Identical monitoring studies performed in all three years have allowed the biological effects and bioaccumulation data to be compared, and in addition, enabled the potential environmental benefits of a PW treatment system (CTour), implemented in 2008, to be evaluated. The results of the 2009 survey showed that caged animals were exposed to low levels of PW components, with highest tissue concentrations in mussels located closest to the PW discharge. Mussels located approximately 1-2 km away demonstrated only background concentrations of target compounds. Concentrations of polycyclic aromatic hydrocarbons (PAH) and alkyl phenol (AP) metabolites in the bile of caged cod were elevated at stations 200-250 m from the discharge. There was also a signal of exposure relative to discharge for the biomarkers CYP1A in fish and micronuclei in mussels. All other fish and mussel biomarkers showed no significant exposure effects in 2009. The mussel bioaccumulation data in 2009 indicated a lower exposure to the PW effluent than seen previously in 2008 and 2006, resulting in an associated general improvement in the health of the caged mussels. This was due to the reduction in overall discharge of PW components (measured as oil in water) into the area in 2009 compared to previous years as a result of the improved PW treatment system. [ABSTRACT FROM AUTHOR]