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Supplemented feeds stimulate immune systems of gilthead sea bream - Responsible Seafood Advocate

Supplemented feeds stimulate immune systems of gilthead sea bream

S. Ceulemans L. Tort J. Rotllant

Barcelona study evaluates the effect of feed supplements on immune indicators

gilthead sea bream
A major aquaculture species in Europe, sea bream are affected by immune suppression associated with cold temperatures.

Gilthead seabream (Sparus aurata) is the top aquacultured marine fish species in Europe, with over 70,000 metric tons (MT) produced in 2001. In colder regions of the Mediterranean, the species is affected by winter disease, a complex syndrome that has been related to cold stress-induced immune suppression.

A recent study at the Universidad Autónoma de Barcelona, Spain evaluated the effect of immune-enhancing feed supplements on the immune indicators of gilthead seabream during prolonged administration and a temperature and photoperiod ramp that simulated winter and early spring.

Nonspecific immune system

In fish, nonspecific immune mechanisms are a first line of defense that – in contrast to mammals – represents a significant part of the fish immune response. If pathogens pass the first barrier of the nonspecific immune system, which includes the skin and mucus, cellular and humoral components are triggered to kill the infectious agents.

When the nonspecific immune response fails to stop an infection, fish develop the disease. This leads to the induction of specific defense mechanisms mediated by macrophages and lymphocytes, and the production of antibodies. The nonspecific immune system plays a role in the activation of the specific immune response, which functions as an immunological memory to prevent new infections caused by past pathogens.

Nutrition and disease 

Nutrition plays an important role in the development of an adequate immune response. The amount of nutrients supplied in the diet for normal growth may not be sufficient to support an optimal response by the immune system. Furthermore, antinutritional factors, mycotoxins, and nutritional imbalances can have adverse effects on the capability of fish to resist infection. Many studies have shown that health and immunology are dependent on an adequate supply of key nutrients like vitamins, phospholipids, essential fatty acids, nucleotides, trace minerals and carotenoids.

Immunostimulants

Several compounds, mostly derived from the cell envelopes of microorganisms, have been identified as immunostimulants. The efficacy of immunostimulants to improve resistance to stress and disease strongly depends on the type of compound and supply of adjuvant nutrients essential to support the build-up of the immune system.

Experimental design

Seabream of 70 to 80 grams were stocked in 500-liter tanks (two tanks per treatment) at a density of 6 kilograms per cubic meter. Fish were fed twice daily according to standard feeding tables. Feeding was stopped when the fish refused to eat. Nitrite, ammonia, and pH were kept within acceptable limits for seabream. During the trial, no diseases or infections were observed.

Blood sampling, preparation

Blood was sampled from eight fish per treatment at the start of the test (S1), after four weeks feeding at a constant temperature of 18 degrees-C (S2), after gradual temperature decrease to 11 degrees C (S3), after two weeks at 11 degrees C (S4), and after gradual temperature increase up to 18 degrees-C (S5). The photoperiod simulated the natural photoperiod, starting as 13 hours light per 11 hours dark and decreasing progressively to 11 light per 13 dark at the end of the experiment.

For blood sampling, fish were placed in anesthetic and sampled through caudal puncture with a syringe. Fresh blood was placed in heparinized tubes for nitro-blue tetrazolium determination and lymphocyte count. The rest of the blood was left to clot at 4 degrees-C for two hours. After removing the clot by centrifugation, the serum was aliquoted and deep frozen until the analytical determinations of lysozyme, complement, and agglutination (Fig. 1).

gilthead sea bream
Fig. 1: Tort et al. (1996, 1998) outlined the following immune indicators used to determine the immune status of seabream.
  • Lymphocyte number: Count of white blood cells responsible for proliferation and synthesis of antibodies following an infection.
  • Phagocytosis: Process responsible for the elimination of infectious organisms, initiated by a liberation of free radicals by granulocytes during the so-called “respiratory burst,” which results in a strong microbicidal action. Evaluated by the color change of nitro blue tetrazolium.
  • Lysozyme: Enzyme capable of killing bacteria by breaking the peptidoglycan layers of the bacterial cell envelope.
  • Complement: Complex of soluble factors involved in the direct elimination of infectious organisms and enhancement of the specific immune system.
  • Agglutination: Specific mechanism induced by agglutinating molecules in the serum (immunoglobulins and lectins), which may agglutinate antigens and thus prevent the activity of pathogens.
  • Immunoglobulins: Proteins in IgM fish that act specifically against pathogens.

Experimental feeds

gilthead sea bream
Fig. 2: Immune indicators of gilthead sea bream after feeding during four weeks at a temperature of 18 degrees-C (sampling point S2) on feeds containing various feed supplements. Data represent average and standard error of eight fish. Different letters denote significant differences at p < 0.1 (Tuckey’s HSD).

A standard diet for sea bream (48 percent protein, 17 percent fat) incorporating herring meal, soybean flour and meal, wheat flour, wheat gluten, fish oil, and a 1 percent vitamin-mineral premix was used as a base formulation. In a control diet, 2.5 percent cellulose was added as filler, while the experimental feeds used three feed supplements at 2.5 percent inclusion:

  • Glucan, a supplement based on purified betaglucan
  • Supplement based on treated yeast
  • Aquastim-F, a commercial feed supplement with a blend of natural immunostimulating compounds (including betaglucans and mannans) and nutrients (vitamins, amino acids, nucleotides, micronutrients, and antioxidants).

Immunostimulatory activity

After one month of feeding, fish were sampled at the control temperature. Significant differences were not easily detected due to individual variability. Nevertheless, the diet with the commercial feed supplement gave a higher degree of stimulation in the nonspecific defense indicators of lymphocyte count, phagocytic activity, lysozyme activity, and complement than the other feeds.

gilthead sea bream
Fig. 3: Lysozyme activity (Kunits/l).

Lysozyme activity was stimulated in the groups fed the Aquastim- and glucan-based feeds. No changes were observed in specific responses (agglutination activity and immunoglobulin levels) due to the addition of the feed supplements, which could be expected from the absence of infections during the trial. The diet containing the commercial feed supplement showed better immunostimulatory activity at the control temperature (Fig. 2).

Effect of cold shock 

The decrease of temperature from 18 to 11 degrees-C in seven days showed a clear effect in the levels of both nonspecific and specific immune indicators. The temperature change decreased complement and lysozyme (Fig. 3), increased lymphocytes and phagocytosis activity (Fig. 4), and decreased agglutination activity and total immunoglobulins.

Tort et al. (1998) and Padros et al. (1996) observed a similar decrease of complement, plasma lysozyme, and agglutination activity in seabream during an outbreak of winter syndrome in cage cultures in northeast Spain. Increased immunocompetence, which suggests a better degree of protection, was noted in animals fed the diets containing the glucan and Aquastim.

Maintaining phagocytosis and lysozyme activity

gilthead sea bream
Fig. 4: Phagocytosis (mmol nbt reduction).

Fish maintained at 11 degrees-C for two weeks after the cold shock showed lower values in phagocytosis and lysozyme activity. The experimental feed supplements enhanced these immune indicators differently. The Aquastim-based feed produced enhanced levels of both phagocytosis and lysozyme activity. The glucan- and treated yeast diets resulted in a moderate increase of phagocytosis, and only the treated yeast boosted lysozyme activity.

No differences among groups were observed for agglutination and immunoglobulin levels. These parameters recovered during the course of the cold period regardless of the dietary treatment. This indicated that during prolonged exposure to cold, feed supplements can maintain levels of phagocytosis and lysozyme activity.

Figs. 3 and 4: Effect of temperature/photoperiod ramps on immune indicators of gilthead seabream fed nutritional supplements. Temperature (degrees-C) follows the right axis. Data represent average of eight fish. Different letters within the sampling denote significant differences at p < 0.5 (abc) or p > 0.1 (ABC) Tuckey’s HSD test.

Restoring immunocompetency during temperature recovery 

After recuperation from 11 to 18 degrees-C in one week, followed by one more week at 18 degrees-C, specific defense levels recovered and nonspecific indicators showed a recovery that was not complete for complement. The high variability between individuals during this phase of the trial did not allow detecting dietary effects on the immune parameters. However, higher phagocytosis activity seemed to persist in the group whose feed contained the commercial feed supplement, and agglutination levels increased at the end of the temperature rise regardless of the dietary treatment.

Conclusion

The simulation of winter temperature/photoperiod in the laboratory affects both the nonspecific and specific immune indicators of gilthead sea bream. During this study, the inclusion of a feed supplement based on a blend of immune-enhancing compounds and nutrients boosted the nonspecific immune parameters of gilthead sea bream prior to and during a temperature/photoperiod ramp. This boost was less pronounced when feed supplements were based on pure immune stimulants such as betaglucans or treated yeast.

(Editor’s Note: This article was originally published in the October 2002 print edition of the Global Aquaculture Advocate.)

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