Hostname: page-component-cd9895bd7-dzt6s Total loading time: 0 Render date: 2024-12-28T06:08:26.116Z Has data issue: false hasContentIssue false

Dietary vitamin A can improve immune function in heat-stressed broilers

Published online by Cambridge University Press:  01 October 2009

Z. Y. Niu
Affiliation:
College of Animal Science and Technology, Northwest A&F University, Yangling, Shaanxi 712100, P. R. China
F. X. Wei
Affiliation:
College of Animal Science and Technology, Northwest A&F University, Yangling, Shaanxi 712100, P. R. China
F. Z. Liu*
Affiliation:
College of Animal Science and Technology, Northwest A&F University, Yangling, Shaanxi 712100, P. R. China
X. G. Qin
Affiliation:
College of Animal Science and Technology, Northwest A&F University, Yangling, Shaanxi 712100, P. R. China
Y. N. Min
Affiliation:
College of Animal Science and Technology, Northwest A&F University, Yangling, Shaanxi 712100, P. R. China
Y. P. Gao
Affiliation:
College of Animal Science and Technology, Northwest A&F University, Yangling, Shaanxi 712100, P. R. China
*
Get access

Abstract

This experiment was undertaken to evaluate the effect of dietary vitamin A on the performance and immune competence of broilers under heat stress (HS). A total of 180 birds, at 22 days of age, were randomly assigned to be reared either at 24°C (thermoneutral, TN, 24°C, constant) or 24°C to 38°C (heat stress, HS, cycling) until the age of 42 days. Birds were then supplemented with vitamin A at 750, 1500, 15 000 IU/kg. Each of the 2 × 3 factorially arranged treatments were replicated in six cages, each containing five birds. Humoral immunity was assessed by intravenous injection of 7% sheep red blood cells (SRBC) followed by evaluation of serum for antibody titers in primary and secondary responses. Cell-mediated immunity was assessed by using a Sephadax stimulation method to recruit abdominal exudate cells (AEC) to evaluate macrophage phagocytic ability. Body weight (BW) and feed conversion were significantly affected by dietary vitamin A (P < 0.05). HS significantly reduced BW, feed intake and feed conversion (P < 0.05). Numbers of AEC, percentage of macrophages in AEC, phagocytic macrophages, internalized opsonized and unopsonized SRBC were increased by dietary vitamin A (P < 0.05). Both primary and secondary antibody responses were characterized by increasing titers of antibody to SRBC by dietary vitamin A when birds were exposed to HS (P < 0.05). Lymphoid organ weights, antibody responses, incidence of macrophages in AEC and phagocytic ability of macrophages were all significantly reduced under HS. These results indicated that HS severely reduced performance and immunocompetence of broilers, whereas the immune response of broilers improved by dietary vitamin A supplementation under HS.

Type
Full Paper
Copyright
Copyright © The Animal Consortium 2009

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Austic, RE 1985. Feeding poultry in hot and cold climates. In Stress Physiology in livestock (ed. MK Yousef), vol. 3, pp. 123136. CRC Press, Boca Raton, FL.Google Scholar
Bartlett, JR, Smith, MO 2003. Effects of different levels of zinc on the performance and immunocompetence of broilers under heat stress. Poultry Science 82, 15801588.CrossRefGoogle ScholarPubMed
Bauman, DE, Currie, WB 1980. Partitioning of nutrients during pregnancy and lactation: a review of mechanisms involving homeostasis and homeorhesis. Journal of Dairy Science 63, 15141529.CrossRefGoogle ScholarPubMed
Bowman, TA, Goonewardene, IM, Pasatiempo, AMG, Ross, CA, Taylor, CE 1990. Vitamin A deficiency decreases natural killer cell activity and interferon production in rats. The Journal of Nutrition 120, 12641273.Google ScholarPubMed
Davis, CY, Sell, JL 1983. Effects of all-trans retinol and retinoic acid nutriture on the immune system of chicks. The Journal of Nutrition 113, 19141919.CrossRefGoogle ScholarPubMed
Donker, RA, Nieuwland, MGB, van der Zijpp, AJ 1990. Heat-stress influences on antibody production in chicken lines selected for high and low immune responsiveness. Poultry Science 69, 599607.CrossRefGoogle ScholarPubMed
Friedman, A, Meidovsky, A, Leitner, G, Sklan, D 1991. Decreased resistance and immune response to Escherichia coli infection in chicks with low or high intakes of vitamin A. The Journal of Nutrition 121, 395400.CrossRefGoogle ScholarPubMed
Friedman, A, Sklan, D 1989a. Impaired T lymphocyte immune response in vitamin A depleted rats and chicks. British Journal of Nutrition 62, 439449.CrossRefGoogle ScholarPubMed
Friedman, A, Sklan, D 1989b. Antigen-specific immune response impairment in the chick as influenced by dietary vitamin A. The Journal of Nutrition 119, 790795.CrossRefGoogle ScholarPubMed
Geraert, PA, Padilha, JCF, Guillaumin, S 1996. Metabolic and endocrine changes induced by chronic heat exposure in broiler chickens: growth performance, body composition and energy retention. British Journal of Nutrition 75, 195204.Google ScholarPubMed
Kelley, KW 1985. Immunological consequences of changing environmental stimuli. In Animal stress (ed. G Moberg), pp. 195223. American Physiological Society, Bethesda, MD.Google Scholar
Kucuk, O, Sahin, N, Sahin, K 2003. Supplemental zinc and vitamin A can alleviate negative effects of heat stress in broiler chickens. Biological Trace Element Research 94, 225235.CrossRefGoogle ScholarPubMed
Lepage, KT, Bloom, SE, Taylor, RL Jr 1996. Antibody response to sheep red blood cells in a major histocompatibility (B) complex aneuploid line of chickens. Poultry Science 75, 346350.CrossRefGoogle Scholar
Lessard, M, Hutchings, D, Cave, NA 1997. Cell-mediated and humoral immune responses in broiler chickens maintained on diets containing different levels of vitamin A. Poultry Science 76, 13681378.CrossRefGoogle ScholarPubMed
Lin, H, Wang, LF, Song, JL, Xie, YM, Yang, QM 2002. Effect of dietary supplemental levels of vitamin A on the egg production and immune responses of heat-stressed laying hens. Poultry Science 81, 458465.CrossRefGoogle ScholarPubMed
Miller, L, Qureshi, MA 1991. Comparison of macrophage function in several commercial broiler genetic lines. Poultry Science 70, 20942101.Google Scholar
Nauss, KM, Newberne, PM 1985. Local and regional immune function of vitamin A-deficient rats with ocular herpes simplex virus (HSV) infections. The Journal of Nutrition 115, 13161324.CrossRefGoogle ScholarPubMed
National Research Council 1994. Nutrient requirements of poultry, 9th revised edition. National Academy Press, Washington, DC.Google Scholar
Qureshi, MA, Dietert, RR, Bacon, LD 1986. Genetic variation in the recruitment and activation of chicken peritoneal marophages. Proceedings of the Society for Experimental Biology and Medicine 181, 560568.CrossRefGoogle Scholar
Regnier, JA, Kelley, KW, Gaskins, CT 1980. Acute thermal stressors and synthesis of antibodies in chickens. Poultry Science 59, 985990.CrossRefGoogle ScholarPubMed
Ross, AC 1992. Vitamin A status: relationship to immunity and the antibody response. Proceeding of the Society for Experimental Biology and Medicine 200, 303320.CrossRefGoogle ScholarPubMed
Sabet, T, Hsia, W, Stanisz, M, El-Domeiri, A, van Altten, P 1977. A simple method for obtaining peritoneal macrophages from chickens. Journal of Immunological Methods 14, 103110.CrossRefGoogle ScholarPubMed
SAS Institute 1995. SAS user’s guide, version 6, 3rd edition. SAS Institute Inc., Cary, NC.Google Scholar
Siegel, HS 1987. Effects of behavioral and physical stressors on immune responses. In Biology of stress in farm animals: an integrative approach (ed. PR Wiepkema and PWM van Adrichem), pp. 3954. Martinus Nijhoff, Dordrecht, The Netherlands.CrossRefGoogle Scholar
Sklan, D, Melamed, D, Friedman, A 1994. The effect of varying levels of dietary vitamin A on immune response in the chick. Poultry Science 73, 843847.CrossRefGoogle ScholarPubMed
Subba Rao, DSV, Glick, B 1970. Immunosuppressive action of heat in chickens. Proceedings of the Society for Experimental Biology and Medicine 133, 445448.CrossRefGoogle Scholar
Thaxton, P, Sadler, CR, Glick, B 1968. Immune response of chickens following heat exposure or injection with ACTH. Poultry Science 47, 264266.CrossRefGoogle ScholarPubMed
Thaxton, P, Siegel, HS 1970. Immunodepression in young chickens by high environmental temperature. Poultry Science 49, 202205.CrossRefGoogle ScholarPubMed
Thaxton, P, Siegel, HS 1972. Depression of secondary immunity by high environmental temperature. Poultry Science 51, 15191526.CrossRefGoogle ScholarPubMed
Trembicki, KA, Qureshi, MA, Dietert, RR 1984. Avian peritoneal exudate cells: a comparison of stimulation protocols. Development and Comparative Immunology 8, 395402.CrossRefGoogle Scholar