Nguyen Thi Kim Ha , Tran Minh Phu * , Duong Thi My Tien , Tran Son Tuyen and Do Thi Thanh Huong

* Corresponding author (tmphu@ctu.edu.vn)

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Abstract

The study aimed to investigate the effect of beta-glucans on hematological, immunoglobulins and stress parameters of striped catfish. The study included two experiments. In the first experiment, experimental fish (16.2±0.74 g) was fed for 30 days with feed containing different beta-glucans concentrations (0, 0.5, 1.0, 1.5, 2 and 2.5 g/kg). Fish blood were collected after 0, 1, 3, 7, 14 and 30 days of feeding for analysis of hematological parameters, whereas glucose, cortisol concentration and total immunoglobulins (Ig) were analyzed before initiating experiment and after 7, 14 and 30 days of feeding. In the second experiment, experimental fish (18.5±0.65 g) was fed beta-glucans (1.0 g/kg feed) for one, two and three weeks. After beta-glucans feeding with different period, fish was crowded stressing at high density (3000 fish/m3) for four hours then transferred into tanks (500 L) at lower density (60 fish/m3) and blood samples were collected after 24, 48 and 72 hours for analysis of glucose, cortisol concentration and Ig. The result of experiment 1 showed that fish fed 1 g beta-glucan/kg feed had significantly higher red blood cells, white blood cells, hemoglobin, hematocrit and Ig compared to other treatments. Blood glucose and cortisol concentration in treatment fed 1.0 g/kg feed were significantly lower compared to other treatments. In the second experiment, the concentration of glucose and cortisol in fish fed beta-glucans (1g/kg feed) for three weeks were significantly lower compared to fish fed beta-glucans for one and two weeks when fish being stressed at high density. In fish fed beta-glucans for three weeks, total immunoglobulins was significantly higher than those of other treatments. In conclusion, the optimal level of beta-glucans adding into diet of striped catfish fingerlings should be 1.0 g/kg which improved fish health and stress resistance
Keywords: Beta-glucans, cortisol, Ig, stress, striped catfish

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References

Ayyaru, G., Arul, V., 2010. Enhancement of the innate immune system and disease resistant activity in Cyprinus carpio by oral administration of beta-glucan and whole cell yeast. Aquaculture Research. 41:884e92.

Bagni, M., Romano, N., Finoia, M.G., Abelli, L., Scapigliati, G., Tiscar, P.G., 2005. Short- and long-term effects of a dietary yeast β-Glucan (Macrogard) and alginic acid (Ergosan) preparation on immune response in sea bass (Dicentrarchus labrax). Fish and Shellfish Immunology. 18: 311–325.

Barros, M.M., Falcon, D.R., Orsi, R.O., Pezzato, L.E., Fernandes Jr, A.C., Guimarães, I.G., Fernandes Jr, A., Padovani, C.R., Sartori, M.M.P., 2014. Non-specific immune parameters and physiological response of Nile tilapia fed b-glucan and vitamin C for different periods and submitted to stress and bacterial challenge. Fish and Shellfish Immunology. 39: 188-195.

Bridle, A.R., Carter, C.G., Morrison, R.N., Nowak, B.F., 2005. The effect of β-glucan administration on macrophage respiratory burst activity and Atlantic salmon, Salmo salar L., challenged with amoebic gill disease-evidence of inherent resistance. Fish Disease. 28: 347–356.

Chang, C-S., Huang, S-L., Chen, S., Chen, S-N., 2013. Innate immune responses and efficacy of using mushroom beta-glucan mixture (MBG) on orange-spotted grouper, Epinephelus coioides, Aquaculture. Fish and Shellfish Immunology. 35: 115-125.

Couso, N., Castro, R., Magarinos, B., Obach, A., Lamas, J., 2003. Effect of oral administration of glucans on the resistance of gilthead seabream to pasteurellosis. Aquaculture. 219: 99–109.

Crumlish, M., Dung, T.T., Turnbull, J.F., Ngoc, N.T.N., Ferguson, H.W., 2002. Identification of Edwardsiella ictaluri from diseased freshwater catfish, Pangasius hypophthalmus (Sauvage), cultured in the Mekong Delta, Vietnam. Journal of Fish Disease. 25: 733-736.

Dalmo, R.A., Ingebrigtsen, K., Bøgwald, J., 1997. Non-specific defence mechanisms in fish, with particular reference to the reticuloendothelial system (RES). Journal of Fish Diseases. 20(4): 241-273.

De Silva, S.S., Phuong, N.T., 2011. Striped catfish farming in the Mekong Delta, Vietnam: a tumultuous path to a global success. Reviews in Aquaculture. 3: 45–73.

Del Rio-Zaragoza, O.B., Fajer Avila, E.J., Almazan Rueda, P., 2011. Influence of β-glucan on innate immunity and resistance of Lutjanus guttatus to an experimental infection of Dactylogyrid monogeneans. Parasite Immunology. 33: 483–494.

Directorate of Fisheries, 2015. Vietnamese fishery production in 2014. Accessed on 5 October 2015. Available at http://www.fistenet.gov.vn/thong-tin-huu-ich/thong-tin-thong-ke/thong-ke-1/tinh-hinh-san-xuat-thuy-san-nam-2014 (in Vietnamese).

Dung, T.T., Ngoc, N.T.N., Thinh, N.Q., Thy, D.T.M., Tuan, N.A., Shinn, A., Crumlish, M., 2008. Common diseases of Pangasius catfish farmed in Viet Nam. Global aquaculture advocate July/August, Health management, 77-78.

Hang, B.T.B., Milla, S., Gillardin, V., Phuong, N.T., Kestemont, P., 2013. In vivo effects of Escherichia coli lipopolysaccharide on regulation of immune response and protein expression in striped catfish (Pangasianodon hypophthalmus). Fish and Shellfish Immunology, 34(1): 339-347.

Hang, B.T.B., Phuong, N.T., Kestemont, P., 2014. Oral administration of Escherichia coli lipopolysaccharide enhances the immune system of striped catfish, Pangasianodon hypophthalmus (Sauvage). Aquaculture Research. 1-10. doi:10.1111/are.12589

Hrubec, T.C., Cardinale, J.L., Smith, S.A., 2000. Heamatology and plasma chemistry reference intervals for culture tilapia (Oreochromis hybrid). Veterinary Clinical Pathology. 29: 7-12.

Hugget, A.S.G., Nixon, D.A., 1957. Use of glucose oxidase, peroxidase and o-dianisidine in determination of blood and urinary glucose. Lancet. 2: 368-79.

Huong, D.T.T., Dat, N.T., Mai, L.T., Thinh, N.Q., Ha, N.T.K., Kestemont, P., Phuong, N.T., 2012. The efficacy of vitamin C on stress reduction of striped catfish (Pangasianodon hypophthalmus) fingerling under transport conditions. Oral presentation at International Fisheries Symposium at Can Tho, Vietnam from 06-08 December 2012.

Jaafar, R.M., Skov, J., Kania, P.W., Kurt, Buchmann., 2011. Dose dependent effects of dietary immunostimulants on rainbow trout immune parameters and susceptibility to the parasite Ichthyophthirius multifiliis. Aquaculture Research and Development, S3:001. DOI:10.4172/2155-9546.S3-001.

Jeney, G., Galeotti, M., Volpatti, D., Jeney, Z., Anderson, D.P., 1997. Prevention of stress in rainbow trout (Oncorhynchus mykiss) fed diets containing different doses of glucan. Aquaculture. 154: 1–15.

Meena, D.K., Das, P., Kumar, S., Mandal, S.C., Prusty, A.K., Singh, S.K., Akhtar, M.S., Behera, B.K., Kumar, K., Pal, A.K., Mukherjee., 2012. Beta-glucan: an ideal immunostimulant in aquaculture (a review). Fish Physiology and Biochemistry. 39(3): 1 - 27.

Milla, S., Mathieu, C., Wang, N., Lambet, S., Nadzialek, S., Massart, S., Henrotte, E., Douxfil, J., Mélard, C., Mandiki, S.N.M., Kestemont, P., 2010. Spleen immune status is affected after acute handling stress but not regulated by cortisol in Eurasian perch, Perca fluviatilis. Fish and Shellfish Immunology. 28: 931-941.

Misra, C.K., Das, B.K., Mukherjee, S.C., Pattnaik, P., 2006. Effect of long term administration of dietary β-glucan on immunity, growth and survival of Labeo rohita fingerlings. Aquaculture. 255: 82–94.

Natt, M.P., Herrick, C.A., 1952. A new blood diluent for counting erythrocytes and leucocytes of the chicken. Poultry Science. 31: 735–738.

Oser, B.L., 1965. Hawk’s Physiological Chemistry. McGraw-Hill, New York, NY. 14th ed., p. 1096.

Phan, L.T., Bui T.M., Nguyen, T.T.T., Gooley G.J., Ingram B.A., Nguyen, H.V., Nguyen, T.P., De Silva, S.S., 2009. Current status of farming practices of striped catfish, Pangasianodon hypophthalmus in the Mekong Delta, Vietnam. Aquaculture. 296: 227-236.

Rowley, A.F., 1990. Collection, separation and identification of fish leucocytes. In: Stolen, J.S., Fletcher, T.C., Anderson, D.P., Roberson, B.S., van Muiswinkel, W.B., editors. Techniques in fish immunology. New York: SOS Publications, 113-136.

Siwicki, A.K., Anderson, D.P., 1993. An easy spectrophotometric assay for determining total protein and immunoglobulin levels in fish sera: correlation to fish health. Techniques in Fish Immunology. (3): 23-30.

Soltanian, S., Adloo, M.N., Hafeziyeh, M., Ghadimi, N., 2014. Effect of β-Glucan on cold-stress resistance of stripe catfish, Pangasianodon hypophthalmus (Sauvege, 1878). Veterinarni Medicina 59(9): 440 – 446.

Tam, N.T., and Nguyet, N.T.K., 2012. Effects of beta-glucans in giant snakehead nursery. Fishery Business, 156. Accessed on 5 October, 2015. Available at http://vietfish.org/20121228100819692p48c62/tac-dung-cua-betaglucan-trong-uong-nuoi-ca-loc-bong.htm (in Vietnamese)

Thuy, D.N., Nguyen, N.L.T., Hung, L.T., 2012. Effect of mannanooligosaccharide in ActigenTM on growth and fish health of (Pangasianodon hypophthalmus). Proceeding of the third national young scientist in aquaculture conference, 24 – 25 March 2012, holding in Hue City, Vietnam, 222 – 229.

Vetvicka, V., Vannucci, L., Petr, S., 2013. The Effects of β – glucan on fish immunity. North American Journal of Medical Sciences. 5(10): 580 – 588.

Volpatti, D., D’Angelo, L., Jeney, G., Jeney, Z., Anderson, D.P., Galeotti, M., 1998. Nonspecific immune response in fish fed glucan diets prior to induce transportation stress. Applied Ichthyology. 14: 201–206.

Weinreb, E.C., 1958. Studies on the histology and histopathology of the rainbow trout (Salmo gairdneri irideus). I. Hematology under normal and experimental conditions of inflammation. Zoologica, N.Y. 43(4): 145-155.

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