Comparative evaluation of early humoral and cytokine responses induced by four commercial infectious bursal disease vaccines in broiler chickens

Document Type : Research Paper

Authors

Department of pathology, College of Veterinary Medicine, Al-Qasim Green University, Babylon 51013, Iraq

Abstract

Objective
Infectious bursal disease virus (IBDV) is an important viral pathogen of broiler chickens because of its tropism for immature B lymphocytes in the bursa of Fabricius and its potential to cause immunosuppression. The current study compared the initial immune responses created by 4 commercially available IBD vaccines in broiler chickens through stimulation of both serological and cytokine responses.
Materials and methods
A total of 250 one-day-old Ross 308 broiler chicks were randomly divided into 5 groups of 50 birds and allocated into their respective treatment received one of four types of commercial vaccine (G1-G4) and the control (G5) (Didn't receive vaccine). The antibody response of the immune system was assessed using indirect ELISA on day 1, 10, 15, 20 and 25. Quantitative RT-PCR (qRT-PCR) was performed on days 1-25 to measure the relative expression of IL-1 beta and IFN-gamma. In addition, the field isolate used (used in challenge study) was identified as containing IBDV by conventional RT-PCR targeting VP2.
Results
The maternal antibody titers for each group are similar at 1 day old. At 10 and 15 days of age, Group 1 had the highest antibody titer with the initial humoral response at those times and approached the highest final titer at 25 days. Both Groups 2 and 3 had an intermediate antibody titer at 20 days of age greater than that of Group 1. The expression levels of IL-1β did not vary significantly between groups but Group 1 had the greatest fold increase as measured by the number of individuals who were part of the analysis. Conversely, the level of IFN-γ expression was significantly different between groups. To summarize, the commercial IBD vaccine candidates examined differed in the timing and the intensity of their resultant immune responses. Of the 3 groups, Group 1 had the most favorable early immunogenicity profile by inducing earlier humoral antibody development, a stronger expression of IFN-γ, and the highest final IgY titer.
Conclusion
The findings suggest the use of integrated immune kinetics could be used as a means to generate comparative immunogenicity data of IBD vaccines in broiler chicken populations.

Keywords


Alkie, T. N., & Rautenschlein, S. (2016). Infectious bursal disease virus in poultry: Current status and future prospects. Veterinary Medicine: Research and Reports, 7, 9-18. https://doi.org/10.2147/VMRR.S68905
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, 10, 85-97. https://doi.org/10.2147/VMRR.S185159
Gewaily, M. S., El-Khyat, F., Tahoon, A. E., Al-Rasheed, M., Abdo, S. E., Gado, A., Elmasry, M., & Ismail, M. M. (2024). Cytokines, serological, and histopathological assessment of recombinant vaccination strategies for combatting infectious bursal disease in broiler chickens. Vaccines, 12(1), Article 27. https://doi.org/10.3390/vaccines12010027
Hamad, M., Hassanin, O., Ali, F. A. Z., Ibrahim, R. S., Abd-Elghaffar, S. K., & Saif-Edin, M. (2020). Comparative study on dynamic and immunopathology of four intermediate-plus infectious bursal disease (IBD) vaccines in commercial broiler chickens. Veterinary Research Communications, 44(3-4), 147-157. https://doi.org/10.1007/s11259-020-09782-z
Khabiri, A., Toroghi, R., Mohammadabadi, M., & Tabatabaeizadeh, S. E. (2025). Whole genome sequencing and phylogenetic relative of a pure virulent Newcastle disease virus isolated from an outbreak in northeast Iran. Letters in Applied Microbiology, 78(4), Article ovaf049. https://doi.org/10.1093/lambio/ovaf049
Legese, L., Wakjira, B., Teshome, T., Woldemichael, D. N., Waktole, H., Regassa, F., & Tufa, T. B. (2022). Comparative immunogenicity evaluation of two infectious bursal disease vaccines commonly used in broiler chickens in Ethiopia. Veterinary Medicine: Research and Reports, 13, 31-38. https://doi.org/10.2147/VMRR.S346659
Liu, H., Zhang, M., Han, H., Yuan, J., & Li, Z. (2010). Comparison of the expression of cytokine genes in the bursal tissues of the chickens following challenge with infectious bursal disease viruses of varying virulence. Virology Journal, 7, Article 364. https://doi.org/10.1186/1743-422X-7-364
Mohammadabadi, M., Akhtarpoor, A., Khezri, A., Babenko, O., Stavetska, R. V., Tytarenko, I., Ievstafiieva, Y., Buchkovska, V., Slynko, V., & Afanasenko, V. (2024). The role and diverse applications of machine learning in genetics, breeding, and biotechnology of livestock and poultry. Agricultural Biotechnology Journal, 16(4), 413-442. https://doi.org/10.22103/jab.2025.24662.1644
Naqi, S. A., Marquez, B., & Sahin, N. (1983). Maternal antibody and its effect on infectious bursal disease immunization. Avian Diseases, 27(3), 623-631. https://pubmed.ncbi.nlm.nih.gov/6314972/
Qin, Y., & Zheng, S. J. (2017). Infectious bursal disease virus-host interactions: Multifunctional viral proteins that perform multiple and differing jobs. International Journal of Molecular Sciences, 18(1), Article 161. https://doi.org/10.3390/ijms18010161
Raj, G. D., Rajanathan, T. M., Kumanan, K., & Elankumaran, S. (2011). Changes in the cytokine and Toll-like receptor gene expression following infection of indigenous and commercial chickens with infectious bursal disease virus. Indian Journal of Virology, 22(2), 146-151. https://doi.org/10.1007/s13337-011-0053-0
Shahdadnejad, N., Mohammadabadi, M. R., & Shamsadini, M. (2016). Typing of Clostridium perfringens isolated from broiler chickens using multiplex PCR. Genetics in the Third Millennium, 14(4), 4368-4374.
Sharma, K., Kim, I. J., Rautenschlein, S., & Yeh, H. Y. (2005). Molecular characterization of infectious bursal disease virus isolates from Nepal based on hypervariable region of VP2 gene. Veterinary Microbiology, 109(1-2), 63-71. https://pubmed.ncbi.nlm.nih.gov/15929400/
Solano, W., Giambrone, J. J., Williams, J. C., Lauerman, L. H., Panangala, V. S., & Garces, C. (1986). Effect of maternal antibody on timing of initial vaccination of young White Leghorn chickens against infectious bursal disease virus. Avian Diseases, 30(3), 648-652. https://pubmed.ncbi.nlm.nih.gov/3028351/
Wang, W., Wu, J., Jiang, N., Liang, Q., Liu, R., Fu, Q., Fu, G., Wei, T., Wan, C., Cheng, L., Huang, Y., He, X., Wei, P., & Chen, H. (2025). Advances in infectious bursal disease virus vaccines-A review. Microorganisms, 13(12), Article 2801. https://doi.org/10.3390/microorganisms13122801