DOI QR코드

DOI QR Code

Effects of β-Glucan Supplementation on Lymphocyte Proliferation, Macrophage Chemotaxis and Specific Immune Responses in Broilers

  • Cheng, Yeong-Hsiang (Department of Animal Science, National I-Lan University) ;
  • Lee, Der-Nan (Department of Animal Science, National I-Lan University) ;
  • Wen, Chiu-Ming (Department of Life Science, National Kao-Hsiung University) ;
  • Weng, Ching-Feng (Institute of Biotechnology, National Dong Hwa University)
  • Received : 2003.10.22
  • Accepted : 2004.04.26
  • Published : 2004.08.01

Abstract

Immunomodulatory feed additives might offer alternatives to antimicrobial growth promoters in poultry production. This experiment was carried out to test the effect of $\beta$-glucan supplementation on the growth performance and immune response in broilers. Total of 160 day-old broilers were randomly assigned to 4 treatment groups fed corn-soybean diets containing 0, 0.012, 0.025 or 0.05% of $\beta$-glucan supplement in a 6 week feeding experiment. Growth performance, antibody titer against New Castle vaccine, lymphocyte blastogensis, and peritoneal macrophage chemotaxis activity of broilers were evaluated. Results showed that there were no significant differences in weight gain and feed efficiency among the treatments, and no differences in antibody titer was observed. Supplementation of $\beta$-glucan did not elevate the lymphocyte blastogensis among treatments, following stimulation with different mitogens. However, supplementation with 0.025 and 0.05% $\beta$-glucan enhanced the macrophage chemotaxis activity of broilers. These results suggest that $\beta$-glucan may enhance some cell-mediated immune responses of chickens by modulate macrophages ability.

Keywords

References

  1. Albina, J. E., J. A. Abate and W. L. Henry. 1991. Nitric oxide production is required for murine resident peritoneal macrophages to suppress mitogen-stimulated T cell proliferation: Role of IFN-r in the induction of the nitric oxidesynthesizing pathway. J. Immunol.147:144-148.
  2. Adachi, Y., M. Okazaki, N. Ohno and T. Yadomae. 1994. Enhancement of cytokine production by macrophages stimulated with (1,3)-$\beta$-D-glucan, grifolan (GRN), isolated from Grifola frondosa. Biol. Pharm. Bull. 17:1554-1560.
  3. Babineau, T. J., P. Marcello, W. Swails, A. Kenler, B. Bistrian and R. A. Forse. 1994. Randomised phase I/II trial of a macrophage-specific immunomodulator (PGG-Glucan) in high-risk surgical patients. Ann. Surg. 220:601-609.
  4. Burgaleta, C., M. C. Territo, S. G. Quan and D. W. Golde. 1978. Glucan-activated macrophages: Functional characteristics and surface morphology. J. Reticuloendothel. Soc. 23:195-204.
  5. Chen, H. L., D. F. Li, B. Y. Chang, L. M. Gong, X. S. Piao, G. F. Yi and J. X. Zhang. 2003. Effects of lentinan on broiler splenocyte proliferation, interleukin-2 production, and signal transduction. Poult. Sci. 82:760-766.
  6. Cheng, Y. S. and Victor F. Pang. 1996. The cytotoxic effect of aflatoxin B1 on duck lymphocytes and the protective effect of $\beta$-carotene. J. Chinese Anim. Sci. 25:195-207.
  7. Ding, A. H., C. F. Nathan and D. J. Stuer. 1988. Release of reactive nitrogen intermediates and reactive oxygen intermediates from mouse peritoneal macrophages. Comparison of activating cytokines and evidence for independent production. J. Immunol. 141:2407-2412.
  8. Dritz, S. S., J. Shi, T. L. Kielian, R. D. Goodband, 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. 73:3341-50.
  9. Hiss, S. and H. Sauerwein. 2003. Influence of dietary ss-glucan on growth performance, lymphocyte proliferation, specific immune response and haptoglobin plasma concentration in pigs. J. Anim. Physiol. Anim. Nutr. 87:2-11.
  10. Kimball, J. W. 1990. Introduction to immunology. pp. 232-345. Macmillan Publishing Co., New York; NY. USA.
  11. Klasing, K. C., D. E. Laurin, R. K. Peng and D. M. Fry. 1987. Immunologically mediated growth depression in chicks: influence of feed intake, corticosterone and interleukin-1. J. Nutr. 117:1629-37.
  12. Liew, F. Y. 1995. Regulation of lymphocytes function by nitric oxide. Curr. Opin. Immunol. 7:396-400. https://doi.org/10.1016/0952-7915(95)80116-2
  13. Liu, Y. J. and Q. Z. Li. 1999. Effect of Lentinan and astragalan on IL-2 inductive activity and lymphocyte proliferation in chicks infected with vMDV. Chinese. J. Vet. Med. 25:3-5.
  14. Navarro-Garcia, F., M. Pedroso and R. Lopez-Revilla. 2000. Immunodulation of rat serum and mucosal antibody response to Entamoeba histolytica trophozoites by $\beta$-1,3-glucan and cholera toxin. Clin. Immunol. 97:182-188.
  15. National Research Council. 1994. Nutrient Requirements of Poultry. 9th ED. National Academy Press, Washington, DC.
  16. Ohno, N., N. Asada, Y. Adachi and T. Yadomae. 1995. Enhancement of LPS triggered TNF-$\alpha$(tumor necrosis factor- $\alpha$) production by (1,3)-$\beta$-D-glucans in mice. Biol. Pharm. Bull. 18:126-133.
  17. Ohno, N., Y. Egawa, T. Hashimoto, Y. Adachi and T. Yadomae. 1996. Effect of $\beta$-glucans on the nitric oxide synthesis by murine peritoneal macrophages in vitro. Biol. Pharm. Bull. 19:608-612.
  18. Onderdonk, A. B., R. L.Cisneros, P. Hinkson and G. Ostroff. 1992. Anti-infective effect of poly-$\beta$1-6-glucotrioyl-$\beta$1-3- glucopyranose glucan in vivo. Infect. Immun. 60:1642-1647.
  19. Poutsiaka, D. D., M. Mengozzi, B. Sinha and C. A. Dinarello. 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.
  20. Qureshi, M. A., R. R. Dietert and L. D. Bacon. 1986. Genetic variation in the recruitment and activation of chicken peritoneal macrophage .Proc. Soc. Exp. Biol. Med. 181:560-566.
  21. Rabertsen, B., G. Rorstad, R. Engstad and J. Raa. 1990. Enhancement of non-specific disease resistance in Atlantic salmon. Atlantic salmon L., by a glucan form Sachromyces cerevisiae cell walls. J. Fish Dis. 13:878-884.
  22. Ramamoorthy, L., M. C. Kemp and I. R. Tizard. 1996. Acemannan, a $\beta$-(1,4)-acetylated mannan, induces nitric oxide production in macrophage cell line RAW 2647. Mol. Pharmacol. 50:878-884.
  23. SAS. 1989. SAS/STAT Guide for personal computers. Release 6.03th Edition. SAS Institute Inc. Cary, NC, USA.
  24. Schoenherr, W. D., D. S. Pollmann and J. A. Coalson. 1994. Titration of $MacroGard^{TM}$-S on growth performance of nursery pigs. J. Anim. Sci. 72 (Suppl. 2):57 (Abstr.).
  25. Skamene, E. and P. Gros. 1983. Role of macrophages in resistance against infectious disease. Clinic. Immunol. Allergy 3:539-560.
  26. Talebi, A. P., R. Torgerson and G. Mulcahy. 1995. Optimal conditions for measurement of blastogenic responses of chickens to concanavalin A in whole blood assays. Vet Immunol Immunopathol. 46:293-301.
  27. Trembicki, K. A., M. A. Qureshi and R. R. Dietert. 1984. Avian peritoneal exudate cells: a comparison of stimulation protocols. Dev. Comp. Immunol. 8:395-402.
  28. Williams, D. L., T. S. Stahly and D. R. Zimmerman. 1994. Impact of immune system activation on growth and amino acid needs of pigs from 6 to 114 kg body weight. J. Anim. Sci. 72:57 (Abstract).
  29. Wu, M. C., L. C. Wung, C. C. Liao, C. C.Kuo and F. S. Chang. 1997. Effect of dietary egg white product and MacroGard on growth performance and immune response in wealing pigs. J. Anim. Ind. Res. 3:17-33.

Cited by

  1. on growth performance and immunocompetence in weanling pigs vol.62, pp.1, 2008, https://doi.org/10.1080/17450390701780201
  2. Effect of dietary supplementation of probiotic on the performance of F1 crossbred (Rhode Island red male × Fayoumi female) cockerels vol.95, pp.4, 2011, https://doi.org/10.1111/j.1439-0396.2010.01079.x
  3. Assessing the effect of administering different probiotics in drinking water supplement on broiler performance, blood biochemistry and immune response vol.39, pp.4, 2011, https://doi.org/10.1080/09712119.2011.623783
  4. extract to diets of layer chicks vol.52, pp.5, 2011, https://doi.org/10.1080/00071668.2011.619517
  5. Respostas fisiológicas e de desempenho de leitões suplementados com B-glucanos e desafiados imunologicamente vol.64, pp.2, 2012, https://doi.org/10.1590/S0102-09352012000200025
  6. Immunomodulatory efficacy of yeast cell products in poultry: a current review vol.70, pp.01, 2014, https://doi.org/10.1017/S0043933914000051
  7. Effects of Bacillus subtilis, Kefir and β-Glucan Supplementation on Growth Performance, Blood Characteristics, Meat Quality and Intestine Microbiota in Broilers vol.43, pp.3, 2016, https://doi.org/10.5536/KJPS.2016.43.3.159
  8. Effects of supplementation of multi-enzyme and multi-species probiotic on production performance, egg quality, cholesterol level and immune system in laying hens vol.39, pp.4, 2011, https://doi.org/10.1080/09712119.2011.621538
  9. Effect of nutritional interventions with quercetin, oat hulls, β-glucans, lysozyme and fish oil on performance and health status related parameters of broilers chickens vol.59, pp.5, 2018, https://doi.org/10.1080/00071668.2018.1496402
  10. Psittacine Circovirus Infection in Parakeets of the Genus Eunymphicus and Treatment with β-(1,3/1,6)-D-Glucan vol.51, pp.4, 2004, https://doi.org/10.1637/7896-013007-caser.1
  11. Anti-adherence of Antibacterial Peptides and Oligosaccharides and Promotion of Growth and Disease Resistance in Tilapia vol.20, pp.4, 2004, https://doi.org/10.5713/ajas.2007.569
  12. The Modulating Effect of β-1, 3/1, 6-glucan Supplementation in the Diet on Performance and Immunological Responses of Broiler Chickens vol.21, pp.2, 2004, https://doi.org/10.5713/ajas.2008.70207
  13. Effect of Dietary β-1,3/1,6-glucan Supplementation on Growth Performance, Immune Response and Plasma Prostaglandin E2, Growth Hormone and Ghrelin in Weanling Piglets vol.21, pp.5, 2004, https://doi.org/10.5713/ajas.2008.70559
  14. Growth Performance and Antibody Response of Broiler Chicks Fed Yeast Derived β-Glucan and Single-strain Probiotics vol.21, pp.7, 2004, https://doi.org/10.5713/ajas.2008.70571
  15. 효모변이균주 유래 β-글루칸과 복합균종 생균제의 혼합급여가 육계의 생산성 및 장내 균총에 미치는 영향 vol.50, pp.1, 2004, https://doi.org/10.5187/jast.2008.50.1.089
  16. Beta-Glucans as Immunomodulators in Poultry: Use and Potential Applications vol.3, pp.4, 2004, https://doi.org/10.3184/175815511x12919999481888
  17. Immune responses to dietary β-glucan in broiler chicks during an Eimeria challenge vol.89, pp.12, 2004, https://doi.org/10.3382/ps.2010-00987
  18. Review: Roles of Prebiotics in Intestinal Ecosystem of Broilers vol.5, pp.None, 2004, https://doi.org/10.3389/fvets.2018.00245
  19. Resolving the pathogenicity factors of a novel opportunistic fungus Schizophyllum commune at molecular level vol.46, pp.4, 2019, https://doi.org/10.1007/s11033-019-04830-7
  20. Effects of dietary supplementation with different levels and molecular weights of fungal β-glucan on performances, health and meat quality in broilers vol.32, pp.10, 2019, https://doi.org/10.5713/ajas.18.0927
  21. Effects of phytogenic feed additives, probiotic and mannan-oligosaccharides on performance, blood metabolites, meat quality, intestinal morphology, and microbial population of Japanese quail vol.61, pp.2, 2020, https://doi.org/10.1080/00071668.2019.1686122
  22. Effects of live yeast (Saccharomyces cerevisiae) as a substitute to antibiotic on growth performance, immune function, serum biochemical parameters and intestinal morphology of broilers vol.49, pp.1, 2004, https://doi.org/10.1080/09712119.2021.1876705
  23. Review: β-glucans as Effective Antibiotic Alternatives in Poultry vol.26, pp.12, 2004, https://doi.org/10.3390/molecules26123560