Antibiotics and malachite green residues in farmed rainbow trout (Oncorhynchus mykiss) from the Iranian markets: A risk assessment

Antibiotic and malachite green residues in farmed rainbow trout muscles were determined by high-performance liquid chromatography for a food risk assessment. The surveillance was carried out on total of 120 rainbow trout fillets, all fishes were randomly sampled from 20 fish markets of Iran. All antibiotics were detected in the range of 0.42–1.20 μg/g for Oxytetracycline, 0.02–0.34 μg/g for Enrofloxacin, 0.21–2.61 μg/g for Florfenicol, and finally 0.02–0.89 μg/g for Malachite green. Our results showed that 99 (82.5%), 36 (30%), 56 (46.6%), and 70 (58.4%) samples contained detectable residues of Oxytetracycline, Enrofloxacin, and Florfenicol antibiotics, and Malachite green, respectively. Our results showed that fish farmers use these drugs in large scale. Further investigations are needed to prevent: the foodborne risk to consumers, the possible environmental contamination, and the antimicrobial resistances.     

Differentiation of the rainbow trout (Oncorhynchus mykiss) from Atlantic salmon (Salmon salar) by the AFLP-derived SCAR

A species-specific SCAR marker for rainbow trout, which was used to detect adulteration and fraudulent labeling in Atlantic salmon products, has been developed based on the AFLP analysis and evaluated in this study. The SCAR marker could be amplified and visualized in 1% agarose gel in all tested rainbow trout samples and absent in all salmon samples. Using DNA admixtures, the detection of 1% (0.5 ng), 10% (5 ng) rainbow trout DNA in Atlantic salmon DNA for fresh and processed samples, respectively was readily achieved. The molecular approach was sensitive and demonstrated to be a rapid and reliable method for identifying frauds in salmon products and could be extended for applications of species identification in food industry.     

Influence of environmental temperature on composition of lipids in edible flesh of rainbow trout (Oncorhynchus mykiss)

The adaptative changes in the fatty acid composition of the main lipid classes in rainbow trout (Oncorhynchus mykiss) edible flesh in response to environmental variation in water temperature were investigated. The research was carried out on intensively farmed trout sampled at different times of the year. Neutral lipids (NL), phosphatidylcholine (PC) and phosphatidylethanolamine (PE) were separated using flash chromatography. Compared with summer acclimatisation, a decrease in neutral lipids of about 19% was observed in winter, accompanied by increases in phosphatidylethanolamine and phosphatidylcholine of about 41 and 29%, respectively. The metabolic adjustment in cold adaptation caused an increase in the levels of unsaturated fatty acids and monoenes of the oleic acid ω9 family and an increase in the levels of unsaturated fatty acids of the linoleic acid ω3 family. At the same time a reduction in the levels of saturated and monounsaturated fatty acids of the oleic acid ω9 family was observed. This pattern turned out to be particularly evident in phosphatidylcholine. The net result of these changes in composition was a significant increase in the polyunsaturated/saturated and polyunsaturated/monoenic fatty acid ratios in the edible flesh. Copyright © 2003 Society of Chemical Industry     

Potential use of a microalga (Chlorella vulgaris) in the pigmentation of rainbow trout (Oncorhynchus mykiss) muscle

The main purpose of this work was to evaluate the colouring effect of carotenoids present in dry biomass obtained from stressed cells ofChlorella vulgaris. Total carotenoids represented only 0.2% of dry algal biomass and consisted mainly of canthaxanthin, lutein, astaxanthin and their esters. — A rainbow trout feeding trial was conducted in order to investigate the effects of dietary algal incorporation as a pigment source, in comparison to that obtained with synthetic pigments, both astaxanthin and canthaxanthin. — The colour intensities measured in muscle were compared, in each case, with those which constitute the Salmonids Roche Colour Card, and proved similar after both 3 and 6 weeks feeding, with a significant increase detected, but at the end of experiment (9 weeks) the increase was shown only in spectrophotometric (quantitative) results.Chlorella vulgaris biomass, which is storable without any special precautions, thus appears to be a promising source of carotenoids to use in commercial fish finishing diets, quite comparable in efficiency with the existing synthetic pigments. Algal biomass micronization, which was also tried out, was not found to be advantageous for the efficiency of colouring, no evidence having been found of any difference in its absorption and in the distribution of pigment through muscle, even if a 150-g rainbow trout, which has a rather short digestive tract, was used.     

Effect of gamma irradiation and frozen storage on chemical and sensory characteristics of rainbow trout (Oncorhynchus mykiss) fillet

The present study was conducted to evaluate the combined effect of low‐dose gamma irradiation (1, 3 and 5 kGy) and frozen storage (5 months at ?20 °C) on chemical and sensory characteristics of rainbow trout (Oncorhynchus mykiss) fillet. Our statistical analysis showed that irradiation process and frozen storage time had a significant effect (P < 0.05) on total volatile nitrogen (TVN), peroxide value (PV), thiobarbituric acid (TBA) and pH. The level of all of these factors increased with increasing frozen storage time. At the end of the fifth month of frozen storage, the lowest and the highest level of TVN, PV and TBA were corresponding to the irradiated samples at 3 and 5 kGy, respectively. In terms of the overall acceptability of their texture, odour, colour and taste, irradiated samples at 3 kGy had the best quality and remained acceptable after 5 months frozen storage. The optimum dose of gamma radiation of rainbow trout fillets according to chemical and sensory analysis was obtained at 3 kGy.     

Investigation of the sensory properties of the flesh of rainbow trout (Oncorhynchus mykiss) fed diets with astaxanthin, shrimp waste meal and red pepper meal

Sensory properties (colour, general appearance and taste) were investigated in rainbow trout, Oncorhynchus mykiss, fed standard diets supplemented with either 60 mg/kg astaxanthin, shrimp waste meal or red pepper meal. The fish were divided into three experimental groups (fed diets supplemented with pigments) and one control group, and fed experimental and control diets for 100 days. After the feeding period, the fish were evaluated for sensory properties. Colour was evaluated using a colour card for salmonids. General appearance and taste were evaluated using hedonic scaling. Significant differences between the fish fed diets with and without pigment supplementation were found. Feeding of rainbow trout with diets supplemented with pigments affected their sensory properties.     

Tissue distribution and residue depletion of metronidazole in rainbow trout (Oncorhynchus mykiss)

Tissue distribution and residue depletion of metronidazole (MNZ) was studied in rainbow trout (Oncorhynchus mykiss) following oral administration of MNZ in feed at the average dose of 25 mg kg^?1 body weight day^?1 for 7 days at 11 ± 2°C. The MNZ concentration in feed was 0.25% while daily feed intake was 1% of body weight. The concentrations of MNZ and its main metabolite, hydroxymetronidazole (MNZOH), in fish tissues were determined by LC-MS/MS. The drug was well distributed in tissues with maximum concentrations on day 1 post-administration. At this time, the mean MNZ concentrations in muscle, skin, kidney, liver and gill were 14 999, 20 269, 15 070, 10 102 and 16 467 µg kg^?1 respectively. MNZ was converted into MNZOH with the ratio of MNZOH:MNZ up to 7% in all fish tissues throughout the withdrawal period. This shows that MNZ itself is the main residue in rainbow trout. MNZ was detected at the level close to the decision limit (0.20 µg kg^?1) in muscle, skin and muscle with adhering skin up to 42 days, while in kidney, liver and gill it was up to 28 days post-administration. MNZOH was eliminated more rapidly from fish tissues and it was present in muscle alone up to 21 days. The elimination half-lives of MNZ and MNZOH in rainbow trout tissues were 1.83–2.53 and 1.24–2.12 days, respectively. When muscle without skin was analysed, higher MNZ and MNZOH concentrations were detected, and for a longer period of time, than in muscle with adhering skin. Thus muscle alone could be more appropriate for the effective residue control of MNZ in rainbow trout. For the same reason, it is also essential to ensure direct cooling immediately after sampling, since MNZ and its metabolite degrade in fish muscle and skin stored in non-freezing conditions.     

Variation in sensory profile of individual rainbow trout (Oncorhynchus mykiss) from the same production batch

The variation in sensory profile of rainbow trout (Oncorhynchus mykiss), belonging to the same aquaculture production batch and handled the same way, was explored by using objective sensory profiling on heat-treated minced fillets. In addition, quality index, mechanical texture, pH, fat, and water content were measured. Different groups of fish were sampled 3 different times during a production day. The results showed significant differences in the sensory profiles of individual fish within all 3 groups as well as significant differences between the groups. Differences in mechanical texture were found between individuals in 2 of the 3 groups and between the groups. No differences were found in quality index neither between individuals nor groups. A significant negative correlation between lipid content and firm texture was observed, but in general, the chemical and physical measurements could not explain the differences in the sensory profiling or in the mechanical texture measurements. The results showed that significant differences in the sensory profiles of individual fish from the same aquaculture production batch may occur. Furthermore, the results also showed sensory differences between groups of samples taken at different times during a production day.     

Effects of diesel on survival, growth, and gene expression in rainbow trout (Oncorhynchus mykiss) fry

Diesel spills are all too frequent disturbances of freshwater ecosystems, largely as a result of the quantities transported and consumed. Assessing the risk that such events may pose to aquatic life remains a difficult process, because of the complexity of this hydrocarbon mixture and our limited knowledge of its toxicity. A diesel spike experiment with rainbow trout (Oncorhynchus mykiss) fry was carried out to fill this knowledge gap. Survival, growth, and gene expression changes were assessed and toxicity thresholds were determined. Whereas the biological end points were consistent in the determination of (sub)lethal doses, microarrays supplied additional information on the mechanism of toxicity (oxygen deprivation) and potential long-term effects (feminization, immune system alterations) of diesel exposure on salmonids. Hemoglobins, prostaglandins, cytochromes, and gluthathion-S-transferases were among the molecular biomarkers proposed for use in future risk assessments based on microarray results. By bridging traditional toxicity testing with recent microarray technologies, this study shows the potential of genomics tools in ecotoxicity studies as well as industrial applications, including risk assessment, in the near future.     

Kinetics of degradation of adenosine triphosphate in chill-stored rainbow trout (Oncorhynchus mykiss)

Trout that had been held in freshwater or in sea water were stored at 0, 5, or 10 °C, and in the case of sea‐water‐held trout, also at 15 °C. Samples were taken during storage for analysis of ATP‐derived metabolites. The kinetics of degradation of ATP were investigated using two mathematical models, one depending on only endogenous enzymes acting in a sequence of consecutive first order reactions, and one assuming inosine was additionally converted to hypoxanthine by bacterial action. The former model adequately fitted the data from trout held in sea water, but the latter model was a better fit to data from the trout held in freshwater. The activation energy of loss of inosine monophosphate was estimated to be 17.4 kcal mol^?1.     

Determination of the exposure parameters that maximise the concentrations of the anaesthetic/sedative eugenol in rainbow trout (Oncorhynchus mykiss) skin-on fillet tissue

Studies were conducted to determine the anaesthetic/sedative concentrations and durations that would maximise anaesthetic/sedative residue concentrations in rainbow trout (Oncorhynchus mykiss) skin-on fillet tissue. Rainbow trout (167–404 g) were exposed to 50 mg l^?1 AQUI-S^® 20E (10% active ingredient, eugenol) in 17°C freshwater for durations up to 1440 min, 100 and 250 mg l^?1 AQUI-S^® 20E for durations up to 240 min, and 500 and 1000 mg l^?1 AQUI-S^® 20E for durations up to 90 min. Fish exposed to 100 mg l^?1 AQUI-S^® 20E for durations of 30, 60, 120 and 240 min had the greatest eugenol concentrations in the fillet tissue, 50, 58, 54 and 62 µg g^?1, respectively. All other exposure concentrations and durations resulted in significantly lower eugenol concentrations, i.e. all < 39 µg g^?1.     

Effect of chitosan edible coating enriched with lemon verbena extract and essential oil on the shelf life of vacuum rainbow trout (Oncorhynchus mykiss)

In this research, the antioxidant and antibacterial characteristics of the chitosan (CH) coating incorporated with lemon verbena essential oil (LVEO) and extract (LVE) on the quality of the rainbow trout packed by vacuum packaging at 4°C were investigated. Samples evaluated include the following: Control, VP, CH, CH-LVE 2%, CH-LVEO 1%, and CH-LVE 1%-LVEO 0.5% for 16 days at 3 days intervals. All of the samples significantly reduced Psychrotrophic bacteria, total viable counts, Enterobacteriaceae, and H₂S producing bacteria as compared with control during keeping time. Thiobarbituric acid reactive substance, peroxide value, total volatile basic nitrogen, and pH value were detected lower in all of the samples than control. CH incorporated with LVE and LVEO gave an agreeable effect on sensory characteristics. Samples containing CH-LVE 1%-LVEO 0.5% was often in priority by sensory assessors. Generally, LV can be applied as a substitution for chemical preservatives in fish meat.     

Activities of antioxidant enzymes in rats fed with hot-smoked rainbow trout (Oncorhynchus mykiss)

The activities of antioxidant enzymes in rats fed with hot‐smoked rainbow trout (Oncorhynchus mykiss) was investigated. Four diets containing fresh and hot‐smoked rainbow trout flesh and vitamin were prepared and commercial pellet food purchased. Four groups of rats were fed with the diets for 28 days. Body weight was checked weekly. No significant (P > 0.05) differences were found in weight between groups. Malondialdehyde (MDA) values of group B and group D were found to be significantly increased (P < 0.05). Differences in glutathione peroxidase (GPX) and glutathione reductase (GR) values were not significant (P > 0.05) between groups. The difference in superoxide dismutase (SOD) and catalase (CAT) values was found to be significant (P < 0.05). The hot smoked process led to significant changes as decreased in the antioxidant enzymes activities. Our results indicate that determination of MDA, GPX, GR, SOD and CAT parameters in blood may help to point out cancer risk in humans.     

Biochemical changes in freshwater rainbow trout (Oncorhynchus mykiss) during chilled storage†

The sensory characteristics and biochemical freshness-indicator contents of rainbow trout (Oncorhynchus mykiss) stored for up to 12 days (a) in ice without previous gutting (group A), (b) in ice after gutting (group B) and (c) under refrigeration (4–5 °C) after gutting and vacuum-packing (group C) were compared. Acceptable freshness was maintained for five days in groups A and C, and for six days in group B. The results indicate that the hypoxanthine ratio ie hypoxanthine content: (inosine monophosphate + inosine + hypoxanthine content) and K₁ ie (inosine + hypoxanthine content): (inosine monophosphate + inosine + hypoxanthine content) are both useful indicators of the freshness of trout stored in ice, regardless of whether or not they have been gutted beforehand. © 1999 Society of Chemical Industry     

A practical quality index method (QIM) developed for aquacultured rainbow trout (Oncorhynchus mykiss)

Quality index method (QIM) was developed for whole (W) and gutted (G) rainbow trout during ice storage. Draft schemes were modified and final schemes consisted of 30 and 15 demerit points, and 12 and 14 days of shelf life was found for whole and gutted rainbow trout, respectively. Linear regression was calculated with storage time and correlation of QI scores was found to be 0.98 and 0.99 for W and G samples, respectively. Moreover, the developed QIM for W and G rainbow trout with this study is a nondestructive and rapid method for the sensory evaluation of rainbow trout.     

Effect of dietary levels of fat, α-tocopherol and astaxanthin on colour and lipid oxidation during storage of frozen rainbow trout (Oncorhynchus mykiss) and during chill storage of smoked trout

 Female rainbow trout (Oncorhynchus mykiss) with an initial weight of 0.8–0.9 kg were raised in two experiments including a total of 2550 fish divided into 17 groups. The fish were raised for 6 months on 13 different feeds (four fish groups were replicates) varying in dietary levels of fat (27% or 32%), astaxanthin (40, 70 or 100 mg astaxanthin/kg feed) and vitamin E (α-tocopherol; 100, 300 or 600 mg all-rac-α-tocopheryl acetate/kg feed). The levels of fat, astaxanthin and α-tocopherol in the fillets all increased with increasing dietary levels of each feed component. Furthermore, astaxanthin deposition was found to be significantly improved by increasing the dietary fat level from 27% to 32%, but was not affected by dietary levels of α-tocopherol. The highest deposition of α-tocopherol was found in fish fed the lowest level of astaxanthin (40 mg/kg), whereas α-tocopherol deposition was unaffected by the dietary fat level. Frozen storage (–28  °C) of gutted, cleaned and glazed raw fish for 18 months significantly reduced astaxanthin and α-tocopherol levels, while lipid oxidation, measured as thiobarbituric acid reactive substances (TBARS) was limited. In the first experiment, the highest TBARS levels were found during frozen storage in fish fed the lowest level of astaxanthin (40 mg/kg versus 70 mg/kg or 100 mg/kg); unaffected by dietary levels of α-tocopherol (100 mg/kg versus 600 mg/kg), whereas the dietary astaxanthin level (70 mg/kg versus 100 mg/kg) did not influence lipid oxidation in frozen fish in the second experiment. After brine injection, fillets of fish were smoked and a vacuum-packed (95%), sliced product in a transparent laminate was produced. The quality (pigmentation and lipid oxidation) during 3 weeks of illuminated, chill storage (3  °C) was compared for smoked products produced from fresh fish and from fish stored at –28  °C for 12 months and 18 months. Smoked fillets from fish fed 32% fat were found to be less red than those from fish fed 27% fat, and the astaxanthin content and surface redness of the smoked product decreased during chill storage. Lipid oxidation was pronounced in smoked trout, but a high level of α-tocopherol in the fillet significantly reduced lipid oxidation during chill storage of the smoked product. Lipid oxidation in smoked fillets from fish fed 32% fat was more pronounced than in fish fed 27% fat, but increasing the dietary α-tocopherol level from 300 mg/kg feed to 600 mg/kg feed effectively counteracted the negative effect of the high-fat diet on lipid oxidation in the smoked product. Astaxanthin did not affect lipid oxidation in the chill-stored smoked product, in contrast to the frozen, raw fish. Astaxanthin seems to protect against the very early stages of lipid oxidation, while α-tocopherol is more important as an antioxidant at more advanced stages of lipid oxidation. Received: 8 January 1998 / Revised version: 23 March 1998