Journals / Turkish Journal of Veterinary and Animal Sciences / 2013 / Cilt: 37 - Sayı: 3

The effect of soy oil addition to the diet of broiler chicks on the immune response

Pages
264–270
Publication Date
2013-03-01
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

It was concluded that the addition of soy oil to the diet resulted in retardation of the immune organs weight, change in the immune cells profile, and consequently suppression of the antibody titers against Newcastle disease and infectious bursal disease viruses in broiler chicks.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:The objective of this study was to evaluate antibody titers of challenged broiler chicks fed diets supplemented with soy oil.
📊
Key Findings & Data:In a completely randomized design, 120 chicks were assigned to 3 treatments (isoenergetic and isonitrogenous diets based on corn-soybean meal containing 0%, 2%, or 4% soy oil), with 4 replicates for each treatment and 10 chicks per replicate.
💡
Conclusion & Impact:It was concluded that the addition of soy oil to the diet resulted in retardation of the immune organs weight, change in the immune cells profile, and consequently suppression of the antibody titers against Newcastle disease and infectious bursal disease viruses in broiler chicks.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Key words: Antibody · broiler chick · immune cells

Abstract

The objective of this study was to evaluate antibody titers of challenged broiler chicks fed diets supplemented with soy oil. In a completely randomized design, 120 chicks were assigned to 3 treatments (isoenergetic and isonitrogenous diets based on corn-soybean meal containing 0%, 2%, or 4% soy oil), with 4 replicates for each treatment and 10 chicks per replicate. The challenging program included vaccination against Newcastle disease (B1 vaccine on day 12 by eye drop; Lasota vaccine on days 19 and 32 by drinking) and infectious bursal disease (Gumboro D78 vaccine on days 12 and 24 by eye drop). Blood samples were collected from 2 chicks per replicate at days 21 and 42 of age, and then total and differential white blood cells were counted and antibodies against Newcastle and infectious bursal diseases were measured. At days 21 and 42 of age, 2 chicks per replicate were killed and the bursa of Fabricius and spleen were removed and weighed. White blood cell count was the lowest in chicks fed soy oil-free diet. Inclusion of soy oil to diets resulted in significant increase in cell count. Heterophil-to-lymphocyte ratio, as an index of stress, was lower for chicks fed soy oil-free diet than those fed a diet containing soy oil. Relative weights of the bursa of Fabricius and spleen were the highest in chicks fed soy oil-free diet, but they decreased (P < 0.05) as soy oil levels increased in the diet. At days 21 and 42 of age, antibody titers against Newcastle disease and infectious bursal disease viruses were the highest in chicks fed the soy oil-free diet. Antibody titers decreased (P < 0.05) as soy oil levels increased in the diet. It was concluded that the addition of soy oil to the diet resulted in retardation of the immune organs weight, change in the immune cells profile, and consequently suppression of the antibody titers against Newcastle disease and infectious bursal disease viruses in broiler chicks.

Özet

The objective of this study was to evaluate antibody titers of challenged broiler chicks fed diets supplemented with soy oil. In a completely randomized design, 120 chicks were assigned to 3 treatments (isoenergetic and isonitrogenous diets based on corn-soybean meal containing 0%, 2%, or 4% soy oil), with 4 replicates for each treatment and 10 chicks per replicate. The challenging program included vaccination against Newcastle disease (B1 vaccine on day 12 by eye drop; Lasota vaccine on days 19 and 32 by drinking) and infectious bursal disease (Gumboro D78 vaccine on days 12 and 24 by eye drop). Blood samples were collected from 2 chicks per replicate at days 21 and 42 of age, and then total and differential white blood cells were counted and antibodies against Newcastle and infectious bursal diseases were measured. At days 21 and 42 of age, 2 chicks per replicate were killed and the bursa of Fabricius and spleen were removed and weighed. White blood cell count was the lowest in chicks fed soy oil-free diet. Inclusion of soy oil to diets resulted in significant increase in cell count. Heterophil-to-lymphocyte ratio, as an index of stress, was lower for chicks fed soy oil-free diet than those fed a diet containing soy oil. Relative weights of the bursa of Fabricius and spleen were the highest in chicks fed soy oil-free diet, but they decreased (P < 0.05) as soy oil levels increased in the diet. At days 21 and 42 of age, antibody titers against Newcastle disease and infectious bursal disease viruses were the highest in chicks fed the soy oil-free diet. Antibody titers decreased (P < 0.05) as soy oil levels increased in the diet. It was concluded that the addition of soy oil to the diet resulted in retardation of the immune organs weight, change in the immune cells profile, and consequently suppression of the antibody titers against Newcastle disease and infectious bursal disease viruses in broiler chicks.

🔖

Cite This Article

SADEGHI, A. A., MIRMOHSENI, M., SHAWRANG, P., AMINAFSHAR, M. (2013). The effect of soy oil addition to the diet of broiler chicks on the immune response. Turkish Journal of Veterinary and Animal Sciences, Cilt: 37 - Sayı: 3, 264–270. https://ajindex.com/articles/121773

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (14)

  1. Peck, M.D.: Interaction of lipids with immune function I: Biochemical effects of dietary lipids on plasma membranes. J. Nut. Biochem., 1994; 5: 466–478.
  2. Simopoulos, A.P.: The importance of the ratio of omega-6/ omega-3 essential fatty acids. Biomed. Pharmacother., 2002; 56: 365–379.
  3. Yaqoob, P.: Fatty acids and the immune system: from basic science to clinical applications. Proc. Nut. Soc., 2004; 63: 89–104.
  4. Parmentier, H.K., Nieuwland, M.G.B., Barwegen, M.W., Kwakkel, R.P., Schrama, J.W.: Dietary unsaturated fatty acids affect antibody responses and growth of chickens divergently selected for humoral responses to sheep red blood cells. Poult. Sci., 1997; 76: 1164–1171.
  5. Sijben, J.W.C., de Groot, H., Nieuwland, M.G.B., Schrama, J.W., Parmentier, H.K.: Dietary linoleic acid divergently affects immune responsiveness of growing layer hens. Poult. Sci., 2000; 79: 1106–1115. van Heugten, E., Coffey, M.T., Spears, J.W.: Effects of immune challenge, dietary energy density, and source of energy on performance and immunity in weanling pigs. J. Anim. Sci., 1996; 74: 2431–2440.
  6. Friedman, A., Sklan, D.: Effect of dietary fatty acids on antibody production and fatty acid composition of lymphoid organs in broiler chicks. Poult. Sci., 1995; 74: 1463–1469.
  7. Stulnig, T.M.: Immunomodulation by polyunsaturated fatty acids: Mechanisms and effects. Int. Arch. Allergy Immunol., 2003; 132: 310–321.
  8. Kelley, D.S., Hubbard, N.E., Erickson, K.L.: Regulation of human immune and inflammatory responses by dietary fatty acids. Adv. Food Nut. Res., 2005; 50: 101–138.
  9. De Pablo, M.A., De Cienfuegos, G.A.: Modulatory effects of dietary lipids on immune system functions. Immunol. Cell Biol., 2000; 78: 31–39.
  10. He, X., Yang, X., Guo, Y.: Effects of different dietary oil sources on immune function in cyclophosphamide immunosuppressed chickens. Anim. Feed Sci. Technol., 2007; 139: 186–200.
  11. Allan, W.H., Gough L.E.: A standard haemagglutination inhibition test for Newcastle disease: A comparison of macro and micro-methods. Veterinary Record, 1974; 95: 120–123.
  12. Betz, M., Fox, B.S.: Prostaglandin E inhibits production of Th1 lymphokines but not of Th2 lymphokines. J. Immunol., 1991; 146: 108–113.
  13. Yaqoob, P., Calder, P.C.: The effects of dietary lipid manipulation on the production of murine T cell derived cytokines. Cytokine, 1995; 7: 548–553.
  14. Kearns, R.J., Hayek, M.G., Turek, J.J., Meydani, M., Burr, J.R., Greene, R.J., Marshall, C.A., Adams, S.M., Borgert, R.C., Reinhart, G.A.: Effect of age, breed an