Exposure Of Atlantic Salmon Research Articles

Physiological, molecular, and cellular mechanisms of impaired seawater tolerance following exposure of Atlantic salmon, Salmo salar, smolts to acid and aluminum

We examined the physiological, molecular, and cellular mechanisms of impaired ion regulation in Atlantic salmon, Salmo salar, smolts following acute acid and aluminum (Al) exposure. Smolts were exposed to: control (pH 6.5, 3.4 μg l −1 Al), acid and low Al (LAl: pH 5.4, 11 μg l −1 Al), acid and moderate Al (MAl: pH 5.3, 42 μg l −1 Al), and acid and high Al (HAl: pH 5.4, 56 μg l −1 Al) for two and six days. At each time-point, smolts were sampled directly from freshwater treatment tanks and after a 24 h seawater challenge. Exposure to acid/MAl and acid/HAl led to accumulation of gill Al, substantial alterations in gill morphology, reduced gill Na +/K +-ATPase (NKA) activity, and impaired ion regulation in both freshwater and seawater. Exposure to acid/MAl for six days also led to a decrease in gill mRNA expression of the apical Cl − channel (cystic fibrosis transmembrane conductance regulator I), increased apoptosis upon seawater exposure, an increase in the surface expression of mitochondria-rich cells (MRCs) within the filament epithelium of the gill, but reduced abundance of gill NKA-positive MRCs. By contrast, smolts exposed to acid and the lowest Al concentration exhibited minor gill Al accumulation, slight morphological modifications in the gill, and impaired seawater tolerance in the absence of a detectable effect on freshwater ion regulation. These impacts were accompanied by decreased cell proliferation, a slight increase in the surface expression of MRCs within the filament epithelium, but no impact on gill apoptosis or total MRC abundance was observed. However, MRCs in the gills of smolts exposed to acid/LAl exhibited morphological alterations including decreased size, staining intensity, and shape factor. We demonstrate that the seawater tolerance of Atlantic salmon smolts is extremely sensitive to acute exposure to acid and low levels of Al, and that the mechanisms underlying this depend on the time-course and severity of Al exposure. We propose that when smolts are exposed to acid and moderate to high Al concentrations, impaired seawater tolerance results from extensive gill Al accumulation, damage to the epithelium, reduced MRC and transport protein abundance, and a synergistic stimulation of apoptosis in the gill upon seawater exposure. When smolts are exposed to acid and low levels of Al, loss of seawater tolerance appears to be independent of these mechanisms and may result instead from a shift in the phenotype of MRCs present in the gill epithelium.

Potential physiological effects of pharmaceutical compounds in Atlantic salmon (Salmo salar) implied by transcriptomic analysis

Pharmaceuticals are emerging pollutants widely used in everyday urban activities which can be detected in surface, ground, and drinking waters. Their presence is derived from consumption of medicines, disposal of expired medications, release of treated and untreated urban effluents, and from the pharmaceutical industry. Their growing use has become an alarming environmental problem which potentially will become dangerous in the future. However, there is still a lack of knowledge about long-term effects in non-target organisms as well as for human health. Toxicity testing has indicated a relatively low acute toxicity to fish species, but no information is available on possible sublethal effects. This study provides data on the physiological pathways involved in the exposure of Atlantic salmon as representative test species to three pharmaceutical compounds found in ground, surface, and drinking waters based on the evaluation of the xenobiotic-induced impairment resulting in the activation and silencing of specific genes. Individuals of Atlantic salmon (Salmo salar) parr were exposed during 5 days to environmentally relevant concentrations of three representative pharmaceutical compounds with high consumption rates: the analgesic acetaminophen (54.77+/-34.67 microg L(-1)), the anticonvulsant carbamazepine (7.85+/-0.13 microg L(-1)), and the beta-blocker atenolol (11.08+/-7.98 microg L(-1)). Five immature males were selected for transcriptome analysis in brain tissues by means of a 17k salmon cDNA microarray. For this purpose, mRNA was isolated and reverse-transcribed into cDNA which was labeled with fluorescent dyes and hybridized against a common pool to the arrays. Lists of significantly up- and down-regulated candidate genes were submitted to KEGG (Kyoto Encyclopedia of Genes and Genomes) in order to analyze for induced pathways and to evaluate the usefulness of this method in cases of not completely annotated test organisms. Exposure during 5 days to environmentally relevant concentrations of the selected pharmaceutical compounds acetaminophen, carbamazepine, and atenolol produced differences in the expression of 659, 700, and 480 candidate genes, respectively. KEGG annotation numbers (KO annotations) were obtained for between 26.57% and 33.33% of these differently expressed genes per treatment in comparison to non-exposure conditions. Pathways that showed to be induced did not always follow previously reported targets or metabolic routes for the employed treatments; however, several other pathways have been found (four or more features) to be significantly induced. Energy-related pathways have been altered under exposure in all the selected treatments, indicating a possible energy budget leakage due to additional processes resulting from the exposure to environmental contaminants. Observed induction of pathways may indicate additional processes involved in the mode of action of the selected pharmaceuticals which may not have been detected with conventional methods like quantitative PCR in which only suspected features are analyzed punctually for effects. The employment of novel high-throughput screening techniques in combination with global pathway analysis methods, even if the organism is not completely annotated, allows the examination of a much broader range of candidates for potential effects of exposure at the gene level. The continuously growing number of annotations of representative species relevant for environmental quality testing is facilitating pathway analysis processes for not completely annotated organisms. KEGG has shown to be a useful tool for the analysis of induced pathways from data generated by microarray techniques with the selected pharmaceutical contaminants acetaminophen, carbamazepine, and atenolol, but further studies have to be carried out in order to determine if a similar expression pattern in terms of fold change quantity and pathways is observed after long-term exposure. Together with the information obtained in this study, it will then be possible to evaluate the potential risk that the continuous release of these compounds may have on the environment and ecosystem functioning.

The effects of 4-nonylphenol and atrazine on Atlantic salmon (Salmo salar L) smolts

Abstract Exposure of Atlantic salmon ( Salmo salar L.) smolts in freshwater to environmental levels of the oestrogenic chemical 4-nonylphenol (4-NP) (concentrations 5–20 μl l −1 ) during the peak migration period had no significant effect on gill Na + K + ATPase activity, plasma vitellogenin (VTG) levels or hypoosmoregulatory performance as indicated by survival in sea water. However, where smolts were exposed to mixtures of 4-NP and the pesticide atrazine at concentrations of 5.0/1.0 and 10.0/2.0 μg l −1 , respectively, there were significant differences in the gill Na + K + ATPase activity, plasma Cl − and Na + and increased mortalities when transferred to seawater. Smolts retained for a short period in an estuary with high levels of oestrogenic contamination showed no significant differences in gill Na + K + ATPase activity, plasma vitellogenin (VTG) levels or hypoosmoregulatory performance compared to fish maintained in an adjacent uncontaminated estuary. The results of the study are discussed in relation to the effects of environmental levels of oestrogenic contaminants on smoltification and migration in wild salmon.

Ovulation and egg survival following exposure of Atlantic salmon, Salmo salar L., broodstock to different water temperatures

The timing of ovulation and survival of eggs following exposure of 2-sea-winter Atlantic salmon, Salmo salar L., to different temperature regimes during the spawning season were investigated. Water temperature was either increased from 10 to 13–14°C (warm water), decreased abruptly from 10 to 5–7°C (cold water), or gradually decreased from 10 to 8°C (ambient control) from 1 November onwards. Median ovulation time was delayed by 5 weeks in the warmwater group compared with ambient controls, with 43% of the females remaining non-ovulated at the end of the study. Only minor effects were observed on timing of ovulation in the coldwater group compared with ambient controls. Survival of eggs to the eyed stage was significantly higher in the coldwater group (92·1%), compared with both the ambient control group (84·5%) and the warmwater group (76·6%). The results indicate that high water temperature during the spawning season inhibits ovulation and has a detrimental effect on gamete quality in Atlantic salmon.

Recovery of foraging behavior of atlantic salmon exposed to a simulated commercial application of fenitrothion

Fenitrothion is an organophosphate insecticide, used to control forest pests, that has often been sprayed in areas containing streams inhabited by Atlantic salmon (Salmo salar). This study simulated the exposure of Atlantic salmon during operational spraying of fenitrothion to determine if there would be effects on foraging behavior and the length of time required for recovery from any effect. The foraging sequence of the Atlantic salmon exhibited only minor effects of exposure, and the number of ingested prey was not affected. However, the reaction distance of the salmon to prey decreased significantly for those exposed to fenitrothion. The decline in reaction distance was still evident six weeks after exposure.