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The Modulating Effect of β-1, 3/1, 6-glucan Supplementation in the Diet on Performance and Immunological Responses of Broiler Chickens

  • Zhang, Bo (State Key Laboratory of Animal Nutrition, College of Animal Science and Technology China Agricultural University) ;
  • Guo, Yuming (State Key Laboratory of Animal Nutrition, College of Animal Science and Technology China Agricultural University) ;
  • Wang, Zhong (State Key Laboratory of Animal Nutrition, College of Animal Science and Technology China Agricultural University)
  • Received : 2007.04.11
  • Accepted : 2007.07.23
  • Published : 2008.02.01

Abstract

The object of this trial was to investigate the effect of dietary ${\beta}$-1,3/1,6-glucan supplementation on the performance and immunological response of broiler chickens. Two hundred and forty 1-day old male broilers ($39{\pm}1g$) were separated into six treatments which were given six different feeds containing 0 (control), 25, 50, 75, 100 and 125 mg/kg dietary ${\beta}$-1,3/1,6-glucan supplementation. On days 21 and 42, body weight gain, feed consumption and feed conversation rate were recorded as measures of growth performance. The levels of key cytokines in the immuno-regulating pathway: interleukin-1 (IL-1), interleukin-2 (IL-2), interferon $\gamma$(IFN-$\gamma$, tumor necrosis factor $\alpha$(TNF-$\alpha$, and the concentrations of signal molecules: peripheral blood plasma globulin, serum Immunoglobulin G (IgG) and intestinal secretary Immunoglobulin A (sIgA), were measured as indices of the immune response to determine suitable levels of dietary ${\beta}$-1,3/1,6-glucan supplementation. The results indicated that performance was elevated quadratically with dietary ${\beta}$-1,3/1,6-glucan supplementation. Maximal growth performance and an enhanced immunological response were obtained at a supplemented level of 50 mg/kg.

Keywords

References

  1. Ai, G. P., Y. P. Su and T. M. Cheng. Structure and function of intestinal mucosal immunity. China Immunol. J. 16(4):82-84.
  2. Bahl, A. K. and N. Sorgente. 2002. $Immustim^{\circledR}$, a nutricine biomodulator: Controlling necrotic enteritis without growth promotion antibiotics: A field evaluation. Poult. Sci. 80(Suppl1):116(Abstr.).
  3. Bohn, J. A. and J. N. BeMiller. 1995. (1-3)-$\beta$-D-Glucans as biological response modifiers: A review of structure-functional activity relationships. Carbohydrate Polymers 28:3-14. https://doi.org/10.1016/0144-8617(95)00076-3
  4. Castro, M., N. V. Ralston and T. I. Morqenthaler. 1994. Candida albicans stimulates arachidonic acid liberation from alveolar macrophages through alpha-mannan and beta-glucan cell wall components. Infection and Immunity 62:3138-3145.
  5. Cheng, Y. H., D. N. Lee, C. M. Wen and C. F. Weng. 2004. Effects of $\beta$-glucan supplementation on lymphocyte proliferation, macrophage chemotaxis and specific immune responses in broilers. Asian-Aust. J. Anim. Sci. 17(8):1145-1149. https://doi.org/10.5713/ajas.2004.1145
  6. Cleary, J. A., G. E. Kelly and A. J. Husband. 1999. The effect of molecular weight and beta-1,6-linkages on priming of macrophage function in mice by (1,3)-beta-D-glucan. Immunol. Cell Biol. 77:395-403. https://doi.org/10.1046/j.1440-1711.1999.00848.x
  7. Danielle, A. M., Kerckhoffs and F. Brouns. 2002. Effects on the human serum lipoprotein profile of $\beta$-glucan, soy protein and are flavones, plant sterols and stanols, garlic and tocotrienols. J. Nutr. 132(9):2494-2505. https://doi.org/10.1093/jn/132.9.2494
  8. Dritz, S. S., J. Shi, T. L. Kielian, J. L. Nelssen, M. D. Tokach, M. M. Chengappa, J. E. Smith and F. Blecha. 1995. Influence of dietary $\beta$-glucan on growth performance, nonspecific immunity, and resistance to Streptococcus suis infection in weanling pigs. J. Anim. Sci. 73:3341-3350. https://doi.org/10.2527/1995.73113341x
  9. Gordon, D., J. Brown and S. Gordon. 2001. A new receptor for $\beta$-glucans. Macmillan Magazines 36-37.
  10. Guo, Y. M, R. A. Ali and M. A. Qureshi. 2003. The influence of $\beta$-glucan on immune responses in broiler chicks. Immunopharmacol. Immunotoxicol. 25(3):461-472. https://doi.org/10.1081/IPH-120024513
  11. Hoqaboam, C. M., M. L. Steinhauser and H. Schock. 1998. Therapeutic effects of nitric oxide inhibition during experimental fecal peritonitis: Role of interleukin-10 and monocyte chemo attractant protein1. Infection and Immunity 66:650-655.
  12. Huff, G. R., W. E. Huff, N. C. Rath and G. Tellez. 2006. Limited treatment with $\beta$-1,3/1,6-Glucan improves production values of broiler chickens challenged with escherichia coli. Poult. Sci. 85(4):613-618. https://doi.org/10.1093/ps/85.4.613
  13. Huff, G. R., W. E. Huff, J. M. Balog, P. Holt and N. C. Rath. 2002. Effect of dietary treatment with $\beta$-1,3/1,6-glucan (Immustim) on disease resistance of turkeys challenged with Escherichia coli. Poult. Sci. 80(Suppl. 1):18(Abstr.).
  14. Kramer, D. R., R. M. Sutherland and S. Bao. 1995. Cytokine mediated effects in mucosal immunity. J. Immunol Cell Biol. 73:389-396. https://doi.org/10.1038/icb.1995.61
  15. Kulicke, W-M., A. I. Lettau and H. Thielking. 1997. Correlation between immunological activity, molarmass, and molecular structure of different (1,3)-$\beta$-D-glucans. Carbohydrate Res. 297:135-143. https://doi.org/10.1016/S0008-6215(96)00273-X
  16. Li, Z. Q., Y. M. Guo and J. M. Yuan. 2004. Effects of $\beta$-glucan on performance and immune response of broiler chicks. China Poult. 26(9):39-42.
  17. Liu, Y., Y. M. Guo and J. M. Yuan. 2003. Effects of $\beta$-1,3/1,6- glucan on performance and immune response of broilers. J. China Agric. Univ. 8(1):91-94.
  18. Lowry, V. K., M. B. Farnell, P. J. Ferro, C. L. Swaggerty, A. Bahl, M. H. Kogut. 2005. Purified $\beta$-glucan as an abiotic feed additive up-regulates the innate immune response in immature chickens against Salmonella enterica serovar Enteritidis. Interl J. Food Microbiol. 98:309-318. https://doi.org/10.1016/j.ijfoodmicro.2004.06.008
  19. Mansell, P. W. A., G. Rowden and C. Hammer. 1978. Clinical experiences with the use of glucan. In Immune Modulation and Control of Neoplasia by Adjuvant Therapy. Raven Press, New York, NY.
  20. Mao, X. F., X. S. Piao, C. H. Lai, D. F. Li, J. J. Xing and B. L. Shi. 2005. Effects of $\beta$-glucan obtained from the Chinese herb Astragalus membranaceus and lipopolysaccharide challenge on performance, immunological, adrenal, and somatotropic responses of weaning pigs. J. Anim. Sci. 83:2775-2782. https://doi.org/10.2527/2005.83122775x
  21. National Research Council. 1994. Nutrient requirements of poultry H. 9th Ed. National Academy press, Washington DC.
  22. Pins, J. J., J. M. Keenan, L. L. Curry, M. J. Goulson and L. W. Kolberg. 2005a. Extracted barley beta-glucan improves metabolic control and blood lipid in metabolic syndrome population. Presented at first international congress on prediabetic and metabolic syndrome, Berlin, Germany, April 13-16.
  23. Pins, J. J., J. M. Keenan, M. J. Goulson, L. W. Kolberg and N. E. Knutson. 2005b. Extracted barley betaglucan improves metabolic control and blood lipids in metabolic syndrome population. Poster presented at American College of Nutrition Annual Meeting, Charleston, SC, Sept. 22-25.
  24. Poutsiaka, D. D., M. Menggozzi and E. Vannier. 1993. Cross-linking of the beta-glucan receptor on human monocytes results in interleukin-1 receptor antagonist but not interleukin-1 production. Blood, 82:3695-3700.
  25. Ramaswamy, K., D. N. Correa and R. Bell. 1996. Local intestinal immune responses to infections with trichinella spiralis. J. Immunol. 156(11):4328-4337.
  26. Reynolds, J. A., M. D. Kastello, D. G. Harrington, C. L. Crabbs, C. J. Peters, J. V. Jemski, G. H. Scott and N. R. Di Luzio. 1980. Glucan-induced enhancement of host resistance to selected infectious diseases. Infection and Immunity 30:51-57.
  27. Rinsten, L., T. Stenberg and R. Andersson. 2003. Determination of $\beta$-glucan molecular weight using SEC with calcofluor detection in cereal extracts. Cereal Chemistry, 80(4):485-490. https://doi.org/10.1094/CCHEM.2003.80.4.485
  28. Sakurai, T., K. Hashimoto, I. Suzuki, N. Ohno, S. Oikawa, A. Masuda and T. Yadomae. 1992. Enhancement of murine alveolar macrophage functions by orally administered $\beta$-glucan. Interl J. Immunopharmacol. 14:821-830. https://doi.org/10.1016/0192-0561(92)90080-5
  29. Schoenherr, W. D., D. S. Pollmann and J. A. Coalson. 1994. Titration of macroGards on growth performance of nursery pigs. J. Anim. Sci. 72(Suppl.2):57(Abstr.).
  30. Sohn, K. S., M. K. Kim, J. D. Kim and In. K. Han. 2000. The role of immunostimulants in monogastric animal and fish -review. Asian-Aust. J. Anim. Sci. 13(8):1178-1187. https://doi.org/10.5713/ajas.2000.1178
  31. SPSS Inc. 2001. SPSS user's guide: statistics, Version 11.0.0 Ed (SPSS for Windows, Release 11.0.0).
  32. Suphantharika, M., P. Khunrae and P. Thanardkit. 2003. Preparation of spent brewer's yeast $\beta$-glucan with a potential application as an immunostimulant for black tiger shrimp, Penaeusmomodon. Bioresource Technology 88:55-60. https://doi.org/10.1016/S0960-8524(02)00257-2
  33. Thanardkit, P., P. Khunrae and M. Suphantharika. 2002. Glucan from spent brewer's yeast: preparation, analysis and use as a potential immunostimulant in shrimp feed. World J. Microbiol. Biotechnol. 18:527-539. https://doi.org/10.1023/A:1016322227535
  34. Tokunaka, K., N. Ohno and Y. Adachi. 2000. Immunopharmacological and immunotoxicological activities of a water-soluble (1$\rightarrow$3)- $\beta$-D-glucan, CSBG from Candida spp. Interl J. Immunopharmacol. 22:383-394. https://doi.org/10.1016/S0192-0561(99)00093-4
  35. Tzianabos, A. O. 2000. Polysaccharide immunomodulators as therapeutic agents: Structural aspects and biologic function. Clinic. Microbiol. Reviews 13:523-533. https://doi.org/10.1128/CMR.13.4.523-533.2000
  36. Vetvicka, V. and J-C. Yvin. 2004. Effects of marine $\beta$-glucan on immune reactions. Interl Immunopharmacol. 4:721-730. https://doi.org/10.1016/j.intimp.2004.02.007
  37. Wang, Z., Y. M. Guo and G. Q. Niu. 2006. Effect of $\beta$-1,3/1,6-glucan from Saccharomyces cerevisiae on growth performance and immune function of suckling piglets. China J. Anim. Sci. 42(21):19-22.
  38. Williams, D. L. and N. R. Di Luzio. 1979. Glucan induced modification of experimental Staphylococcus aureus infection in normal, leukemic and immunosuppressed mice. Adv. Experi. Medicine Biol. 121(A):291-306.
  39. Williams, S. B., J. R. Rose, L. Rott, M. A. Franco, H. B. Greenberg, E. C. Butcher. 1998. The memory B cell sunset responsible for the secretory IgA response and protective humoral immunity to rotavirus express the intestinal homing receptor, ${\alpha}4{\beta}7$. J. Immunol. 161(8):4227-4235.
  40. Young, S. H., J. Ye, D. G. Frazer, X. Shi and V. Castranova. 2001. Molecular mechanism of tumor necrosis factor-alpha production in 1-3-$\beta$-glucan (zymosan)-activated macrophages. J. Biol. Chem. 276:20781-20787. https://doi.org/10.1074/jbc.M101111200
  41. Yun, C. H., A. Estrada, A. VanKessel, B-C. Park and B. Laarveld. 2003. Beta-glucan, extracted from oat, enhances disease resistance against bacterial and parasitic infections. FEMS Immunol. Medic. Microbiol. 35:67-75. https://doi.org/10.1016/S0928-8244(02)00460-1

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