Browse > Article
http://dx.doi.org/10.5713/ajas.2008.80056

Effect of Chito-oligosaccharide Supplementation on Immunity in Broiler Chickens  

Deng, Xingzhao (China Agricultural University, Ministry of Agriculture Feed Industry Centre)
Li, Xiaojing (China Agricultural University, Ministry of Agriculture Feed Industry Centre)
Liu, Pai (China Agricultural University, Ministry of Agriculture Feed Industry Centre)
Yuan, Shulin (Food engineering department of Jiangsu food science college)
Zang, Jianjun (China Agricultural University, Ministry of Agriculture Feed Industry Centre)
Li, Songyu (China Agricultural University, Ministry of Agriculture Feed Industry Centre)
Piao, Xiangshu (China Agricultural University, Ministry of Agriculture Feed Industry Centre)
Publication Information
Asian-Australasian Journal of Animal Sciences / v.21, no.11, 2008 , pp. 1651-1658 More about this Journal
Abstract
This study was conducted to determine the effects of dietary supplementation of either 100 mg/kg chito-oligosaccharide (COS) or chlortetracycline (CTC) with corn-soybean-fish meal on immunity in broiler chickens. A total of 147 one-day old male broiler chicks were randomly allocated to 3 treatments with 7 replicate pens per treatment and 7 birds per pen. The experimental diets consisted of a control diet based on corn, soybean and fish meal without COS and any antibiotic supplement and similar diets supplemented with either CTC (80 mg/kg from d 1 to 21 and 50 mg/kg from d 22 to 42) or COS (100 mg/kg from d 1 to 42). During the entire experimental period, all birds had ad libitum access to diets and water. The main immune organ indices, T-lymphocyte proliferation, serum cytokine concentrations, serum NO level and serum iNOS activity were measured on d 21 and d 42. On d 21, broilers fed 100 mg/kg COS had improved (p<0.01) indices of spleen, thymus, and bursa of Fabricius compared with the control and CTC birds. Birds receiving 100 mg/kg COS had higher (p<0.05) serum concentrations of $IL-1{\beta}$, IL-6, IgM, NO and iNOS than birds on the control treatment. Serum $Ca^{2+}$ level of birds fed 100 mg/kg COS tended to be higher (p = 0.049) than in birds fed CTC. On d 42, the birds fed 100 mg/kg COS had higher (p<0.05) concentrations of TNF-${\alpha}$ and IgM in serum than birds in both the CTC and control treatments. Birds fed 100 mg/kg COS had a higher concentration of IFN-$\gamma$ than the control group. In conclusion, dietary supplementation of COS appeared to improve the immunity of broilers by promoting the weight of the main immune organs, increasing IgM secretion, stimulating microphages to release $TNF-{\alpha}$, $IL-1{\beta}$, IL-6 and IFN-$\gamma$, and activating iNOS to induce NO.
Keywords
Chitooligosaccharide (CTC); Immune Organ Indices; Cytokines; NO; Broiler;
Citations & Related Records
Times Cited By KSCI : 4  (Citation Analysis)
Times Cited By Web Of Science : 4  (Related Records In Web of Science)
Times Cited By SCOPUS : 16
연도 인용수 순위
1 Han, K. N., I. K. Kwon, J. D. Lohakare, S. Heo and B. J. Chae. 2007. Chito-oligosaccharides as an alternative to antimicrobials in improving performance, digestibility and microbial ecology of the gut in weanling pigs. Asian-Aust. J. Anim. Sci. 20:556-562.   과학기술학회마을   DOI
2 Kim, H. M., S. H. Hong, S. J. Yoo, K. S. Baek, Y. J. Jeon and S. Y. Choung. 2006. Differential effects of chitooligosaccharides on serum cytokine levels in aged subjects. J. Med. Food 9:427-430.   DOI   ScienceOn
3 Li, X. J., X. S. Piao, S. W. Kim, P. Liu, L. Wang, Y. B. Shen, S. C. Jung and H. S. Lee. 2007. Effects of chito-oligosaccharide supplementation on performance, nutrient digestibility, and serum composition in broiler chickens. Poul. Sci. 86:1107-1114.   DOI
4 Moncada, S., R. M. Palmer and E. A. Higgs. 1991. Nitric oxide: physiology, pathophysiology, and pharmacology. Pharmacol. Rev. 43:109-142.
5 Shapiro, F., I. Nir and D. Heller. 1998. Stunting syndrome in broilers: effect of stunting syndrome inoculum obtained from stunting syndrome affected broilers, on broilers, leghorns and turkey poults. Poult. Sci. 77:230-236.   DOI
6 Tokoro, A., M. Kobayashi, N. Tatewaki, K. Suzuki, Y. Okawa, T. Mikami, S. Suzuki and M. Suzuki. 1989. Protective effect of N-acetylchitohexaose on Listeria monocytogens infection in mice. Microbiol. Immunol. 3:357-367.
7 Wang, X. W., Y. G. Du, X. F. Bai and H. G. Li. 2003. The effect of oligochitosan on broiler gut flora, microvilli density, immune function and growth performance. Acta Zoonutrimenta Sinica. 15:32-35.
8 Qureshi, M. A., C. L. Heggen and I. Hussain. 2000. Avian macrophage: effector functions in health and disease. Dev. Comp. Immunol. 24:103-119.   DOI   ScienceOn
9 Roura, E., J. Homedes and K. C. Klasing. 1992. Prevention of immunologic stress contributes to the growth-promoting ability of dietary antibiotics in chicks. J. Nutr. 122:2283-2290.   DOI
10 Royal, W. A., R. A. Robinson and K. I. Loken. 1970. The influence of chlortetracycline feeding in Salmonellosis in young calves. Vet. Rec. 86:67-69.   DOI   ScienceOn
11 Samarasinghe, K., C. Wenk, K. F. S. T. Silva and J. M. D. M. Gunasekera. 2003. Turmeric (Curcuma longa) root powder and mannanoligosaccharides as alternatives to antibiotics in broiler chicken diets. Asian-Aust. J. Anim. Sci. 16(10):1495-1500.   과학기술학회마을   DOI
12 Yuan, S. L., X. S. Piao, D. F. Li, S. W. Kim, H. S. Lee and P. F. Guo. 2006. Effects of dietary Astragalus polysaccharide on growth performance and immune function in weaned pigs Anim. Sci. 82:1-7.
13 SAS Institute. 1996. SAS User's Guide: Statistics. Version 7.0. SAS Institute, Cary, NC
14 Choi, H. J., J. Ahn, N. C. Kim and H. S. Kwak. 2006. The effects of microencapsulated chitooligosaccharide on physical and sensory properties of the milk. Asian-Aust. J. Anim. Sci. 19:1347-1353.   과학기술학회마을   DOI
15 Yu, Z., L. Zhao and H. Ke. 2004. Potential role of nuclear factor-kappaB in the induction of nitric oxide and tumor necrosis factor-alpha by oligochitosan in macrophages. Int. Immunopharmacol. 4:193-200.   DOI   ScienceOn
16 Zafar, T. A., C. M. Weaver, Y. Zhao, B. R. Martin and M. E. Wastney. 2004. Nondigestible oligosaccharides increase calcium absorption and suppress bone resorption in ovariectomized rats. J. Nutr. 134:399-402.   DOI
17 Zhang, M., T. Tan, H. Yuan and C. Rui. 2003. Insecticidal and fungicidal activities of chitosan and oligo-chitosan. J. Bioact. Compat. Polym. 18:391-400.   DOI   ScienceOn
18 Wu, G. J. and G. J. Tsai. 2004. Cellulase degradation of shrimp chitosan for the preparation of a water-soluble hydrolysate with immunoactivity. Fish. Sci. 70:1113-1120.   DOI   ScienceOn
19 Wu, G. J. and G. J. Tsai. 2007. Chitooligosaccharides in combination with interferon-${\gamma}$ increase nitric oxide production via nuclear factor-${\kappa}B$ activation in murine RAW264.7 macrophages. Food Chem. Toxico. 45:250-258.   DOI   ScienceOn
20 Wu, G. J., H. T. Lin and G. J. Tsai. 2002. Production of chitooligosaccharides from shrimp chitosan with immuneenhancing activity. Adv. Chitin Sci. 5:77-80.
21 Seo, W. G., H. O. Pae, N. Y. Kim, G. S. Oh, I. S. Park, Y. H. Kim, Y. M. Kim, Y. H. Lee, C. D. Jun and H. T. Chung. 2000. Synergistic cooperation between water soluble chitosan oligomers and interferon-${\gamma}$ for induction of nitric oxide synthesis and tumoricidal activity in marine peritoneal macriphages. Cancer Lett. 159:189-195.   DOI   ScienceOn
22 Lambrecht, B., M. Gonze, D. Morales, G. Meulemans and T. P. van den Berg. 1999. Comparison of biological activities of natural and recombinant chicken interferon-gamma. Vet. Immunol. Immunopathol. 70:257-267.   DOI   ScienceOn
23 Lancaster, J. R. Jr. 1992. Nitric oxide in cells. Anim. Sci. 80:248-259.
24 Maeda, Y. and Y. Kimura. 2004. Antitumor effects of various low-molecular-weight chitosans are due to increased natural killer activity of intestinal intraepithelial lymphocytes in sarcoma 180-bearing mice. J. Nutr. 134:945-950.   DOI
25 John, P., M. D. Cooke, J. Victor and M. D. Dzau. 1997. Nitrite oxide synthase: role in the genesis of vascular disease. Ann. Rev. Med. 48:489-509.   DOI   ScienceOn
26 Jung, W. K., S. H. Moon and S. K. Kim. 2006. Effect of chitooligosaccharides on calcium bioavailability and bone strength in ovariectomized rats. Life Sci. 78:970-976.   DOI   ScienceOn
27 Karupiah, G., Q. W. Xie, R. M. L. Buller, C. Nathan, C. Duarte and J. D. MacMicking. 1993. Inhibition of viral replication by interferon-gamma-induced nitric oxide synthase. Sci. 261:1445-1448.   DOI   ScienceOn
28 Xie, Q. W., H. J. Cho, J. Calaycay, R. A. Mumford, K. M. Swiderek, T. D. Lee, A. Ding, T. Troso and C. Nathan. 1992. Cloning and characterization of inducible nitric oxide synthase from mouse macrophages. Sci. 256:225-228   DOI
29 Kobayashi, M., T. Watanabe, S. Suzuki and M. Suzuki. 1990. Effect of N-acetylchitohexaose against Candida albicans infection of tumor-bearing mice. Microbiol. Immunol. 34:413-426.   DOI
30 Kolios, G., V. Valatas and S. G. Ward. 2004. Nitric oxide in inflammatory bowel disease: a universal messenger in an unsolved puzzle. Immunology 113:427-437.   DOI   ScienceOn
31 Ding, A. H., C. F. Nathan and D. J. Stuehr. 1988. Release of reactive nitrogen intermediates and reactive oxygen intermediates from mouse peritoneal macrophages: comparison of activating cytokines and evidence for independent production. J. Immun. 141:2407-2412.
32 Dou, J. L., C. Y. Tan, Y. G. Du, X. F. Bai, K. Y. Wang, and X. J. Ma. 2007. Effects of chitooligosaccharides on rabbit neutrophils in vitro. Carbohyhr. Polym. 69:209-213.   DOI   ScienceOn
33 Chae, S. Y., M. Jang and J. Nah. 2005. Influence of molecular weight on oral absorption of water soluble chitosans. J. Control. Release 102:383-394.   DOI   ScienceOn
34 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 weanling pigs J. Anim. Sci. 83:2775-2782.   DOI
35 Mast, J. and B. M. Goddeeris. 1999. Development of immunocompetence of broiler chickens. Vet. Immunol. Immunop. 70:245-256.   DOI   ScienceOn
36 NRC. 1994. Nutrient requirements of poultry. 9th rev. ed. National Academy Press, Washington, DC.
37 Mori, T., Y. Irie, S. I. Nishimura, S. Tokura, M. Matsuura, M. Okumura, T. Kadosawa and T. Fujinaga. 1998. Endothelial cell responses to chitin and its derivatives. J. Biomed. Mater. Res. 43:469-472.   DOI   ScienceOn
38 Naseem, K. M. 2005. The role of nitric oxide in cardiovascular diseases. Mol. Aspects Med. 26:33-65.   DOI   ScienceOn
39 Nathan, C. 1992. Nitric oxide as a secretory product of mammalian cells. FASEB J. 6:3051-3064.   DOI
40 Huff, G. R., W. E. Huff, N. C. Rath and G. Tellez. 2006. Limited treatment with ${\beta}$-1,3/1,6-Glucan improved production values of broiler chickens challenged with Escherichia coli. Poult. Sci. 85:613-618.   DOI
41 Jeon, Y. J. and S. K. Kim. 2002. Antitumor activity of chitosan oligosaccharides produced in ultrafiltration membrane reactor system. J. Microbio. Biotech. 12:503-507.
42 Jeon, Y. J., F. Shahidi and S. K. Kim. 2000. Preparation of chitin and chitosan oligomers and their applications in physiological functional foods. Food Rev. Int. 16:159-176.   DOI   ScienceOn
43 Jeon, Y. J., P. J. Park and S. K. Kim. 2001. Antimicrobial effect of chitoligosaccharides produced by bioreactor. Carbohydr. Polym. 44:71-76.   DOI   ScienceOn
44 Fraifeld, V., R. Blaicher-Kulick, A. A. Degen and J. Kaplanski. 1995. Is hypothalamic prostaglandin $E_{2}$ involved in avian fever? Life Sci. 56:1343-1346.   DOI   ScienceOn
45 Chen, H., W. G. Hong and X. M. Zang. 2006. Effect of oligochitosan on production performance and immune function of quail. J. Economic Animal. 10:18-21 (In Chinese with English Abstract).
46 Gotoh, T., K. Matsushima and K. Kikuchi. 2004. Preparation of alginate-chitosan hybrid gel beads and adsorption of divalent metal ions. Chemosphere 55:135-140.   DOI   ScienceOn
47 Green, L. C., D. A. Wagner, J. Glogowski, P. L. Skipper, J. S. Wishnok and S. R. Tannenbaum. 1982. Analysis of nitrate, nitrite and [15N] nitrate in biological fluids. Anal. Biochem. 126:131-138.   DOI   ScienceOn
48 Han, Y., L. Zhao, Z. Yu, J. Feng and Q. Yu. 2005. Role of mannose receptor in oligochitosan-mediated stimulation of macrophage function. Int. Immunopharmacol. 5:1533-1542.   DOI   ScienceOn
49 Higuchi, M., N. Higashi, H. Taki and T. Osawa. 1990. Cytolytic mechanisms of activated macrophages. Tumor necrosis factor and L-arginine-dependent mechanisms act synergistically as the major cytolytic mechanisms of activated macrophages. J. Immunol. 144:1425-1431.