EFFECT OF DIFFERENT SCHEDULES OF VACCINES ON GROWTH AND PERFORMANCE OF BROILERS
DOI:
https://doi.org/10.54112/bcsrj.v2024i1.913Keywords:
broiler, vaccination, meat quality, health, immunizationAbstract
A vaccination program is a schedule of vaccinations that varies by nation or property. This study set out to assess the productivity and overall health of broiler chickens with different immunization schedules. From a total of 110 Cobb 500 chickens, three treatment groups—each with six duplicates—were chosen at random. For every treatment group, there were different immunization schedules for Newcastle disease, infectious bronchitis, and infectious bursal disease. On the other hand, broilers in Treatment 2 (T2) received vaccinations against ND+IB on days 3 and 7, whereas broilers in Treatment 3 (T3) received vaccinations against ND+IB on days 7 and 21 as well as IBD on day 14. The grill control group in treatment 1 (T1) was vaccinated against ND+IB and IBD on days 7 and 14, respectively. During the 42-day study period, samples and data were gathered to evaluate the animals' development performance, immunological status, carcass characteristics, and meat quality. T1 broilers fared better than T2 and T3 broilers in terms of growth rate, white blood cell count, carcase features, and meat quality. The results of this study show that immunizing broilers against ND+IB and IBD on days 7 and 14 is the most successful vaccination schedule for broiler production, as demonstrated by the animals' improved health and productivity.
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Abdullah, A., & Matarneh, S. (2010). Broiler performance and the effects of carcass weight, broiler sex, and postchill carcass aging duration on breast fillet quality characteristics. Journal of Applied Poultry Research 19, 46-58.
Aini, I. (2006). “Newcastle Disease.” In Diseases of Poultry in Southeast Asia, edited by M. Zamri-Saad, 225–233. 1st ed. Selangor: UPM Press.
Bansal, G., Singh, V., & Sachan, N. (2011). Carcass quality characteristics of broilers as affected by Dried Poultry Excreta supplementation.
Carisch, L., Stirn, M., Hatt, J. M., Federer, K., Hofmann-Lehmann, R., & Riond, B. (2019). White blood cell count in birds: evaluation of a commercially available method. BMC veterinary research 15, 1-7.
Christensen, V. L. (2009). Development during the first seven days post-hatching. Avian Biology Research 2, 27-33.
Chung, E. L. T., Jesse, F. F. A., Marza, A. D., Ibrahim, H. H., Abba, Y., Zamri-Saad, M., Haron, A. W., Lila, M. A. M., Saharee, A. A., & Omar, A. R. (2019). Responses of pro-inflammatory cytokines, acute phase proteins and cytological analysis in serum and cerebrospinal fluid during haemorrhagic septicaemia infection in buffaloes. Tropical animal health and production 51, 1773-1782.
Chung, E. L. T., Kamalludin, M. H., Jesse, F. F. A., Reduan, M. F. H., Ling, L. W., Mahzan, N. M., Henipah, N. N. M. M. A., Loh, T. C., & Idrus, Z. (2020). Health performance and blood profile changes in commercial broilers supplemented with dietary monocalcium phosphate. Comparative Clinical Pathology 29, 573-579.
Cook, M. E. (1999). Nutritional effects on vaccination. Veterinary vaccines and diagnostics 47, 53-58.
Dey, S., Pathak, D. C., Ramamurthy, N., Maity, H. K., & Chellappa, M. M. (2019). Infectious bursal disease virus in chickens: prevalence, impact, and management strategies. Veterinary Medicine: Research and Reports, 85-97.
Fletcher, D., Qiao, M., & Smith, D. (2000). The relationship of raw broiler breast meat color and pH to cooked meat color and pH. Poultry science 79, 784-788.
Hornick, J.-L., Van Eenaeme, C., Gérard, O., Dufrasne, I., & Istasse, L. (2000). Mechanisms of reduced and compensatory growth. Domestic animal endocrinology 19, 121-132.
Jackwood, M. W. (2012). Review of infectious bronchitis virus around the world. Avian diseases 56, 634-641.
Krams, I., Vrublevska, J., Cirule, D., Kivleniece, I., Krama, T., Rantala, M. J., Sild, E., & Hõrak, P. (2012). Heterophil/lymphocyte ratios predict the magnitude of humoral immune response to a novel antigen in great tits (Parus major). Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology 161, 422-428.
Lilliehöök, I., Wall, H., Tauson, R., & Tvedten, H. (2004). Differential leukocyte counts determined in chicken blood using the Cell‐Dyn 3500. Veterinary clinical pathology 33, 133-138.
Lim Teik Chung, E., Kamalludin, M. H., Jesse, F. F. A., Reduan, M. F. H., Loh, T. C., & Idrus, Z. (2019). Effect of Monocalcium Phosphate Supplementation on the Growth Performance, Carcass Characteristic, Gut Histomorphology, Meat and Bone Quality of Broiler Chickens. Pertanika Journal of Tropical Agricultural Science 42.
Liu, L., Qin, D., Wang, X., Feng, Y., Yang, X., & Yao, J. (2015). Effect of immune stress on growth performance and energy metabolism in broiler chickens. Food and agricultural immunology 26, 194-203.
Lu, Z., He, X., Ma, B., Zhang, L., Li, J., Jiang, Y., Zhou, G., & Gao, F. (2017). Chronic heat stress impairs the quality of breast-muscle meat in broilers by affecting redox status and energy-substance metabolism. Journal of agricultural and food chemistry 65, 11251-11258.
Marangon, S., & Busani, L. (2007). The use of vaccination in poultry production. Revue Scientifique et Technique-Office International des Epizooties 26, 265.
Müller, H., Mundt, E., Eterradossi, N., & Islam, M. R. (2012). Current status of vaccines against infectious bursal disease. Avian pathology 41, 133-139.
Nelson, J. R., McIntyre, D. R., Pavlidis, H. O., & Archer, G. S. (2018). Reducing stress susceptibility of broiler chickens by supplementing a yeast fermentation product in the feed or drinking water. Animals 8, 173.
Petracci, M., Betti, M., Bianchi, M., & Cavani, C. (2004). Color variation and characterization of broiler breast meat during processing in Italy. Poultry science 83, 2086-2092.
SADIQ M. Pakistan poultry sector still. World Poultry. 20, 10–11.
Sahin, A., & Forbes, J. (1999). Corticosterone, dietary fat source and diet selection in relation to body composition. British Poultry Science 40, 52-54.
Scanes, C. G. (2016). Biology of stress in poultry with emphasis on glucocorticoids and the heterophil to lymphocyte ratio. Poultry science 95, 2208-2215.
Sharma, J. (1999). Introduction to poultry vaccines and immunity. Advances in veterinary medicine 41, 481-494.
Virden, W., & Kidd, M. (2009). Physiological stress in broilers: Ramifications on nutrient digestibility and responses. Journal of Applied Poultry Research 18, 338-347.
Wang, X., Zhou, Q., Shen, J., Yao, J., & Yang, X. (2015). Effect of difference doses of Newcastle disease vaccine immunization on growth performance, plasma variables and immune response of broilers. Journal of animal science and biotechnology 6, 1-5.
Yang, X., Li, W., Feng, Y., & Yao, J. (2011). Effects of immune stress on growth performance, immunity, and cecal microflora in chickens. Poultry science 90, 2740-2746.
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Copyright (c) 2024 U RAUF, SU HAQ, Z ARSHAD, M USMAN, M SAJID, SF WAHEED, T HUSSAIN, A HUSSAIN, S AMEER, HAA NAZEER, A ULLAH, A HASSAN, A SABIR
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