The influence of Ross 308 breeder flock age on serum Newcastle Disease Virus and Infectious Bursal Disease Virus antibody levels and their transfer to offspring

Authors

  • M. Wegner Boehringer-Ingelheim, Dziekońskiego St. 3, 00-728 Warsaw, Poland
  • M. Gesek Department of Pathological Anatomy, Faculty of Veterinary Medicine, University of Warmia and Mazury in Olsztyn, Oczapowskiego St. 13, 10-719 Olsztyn, Poland

DOI:

https://doi.org/10.24425/pjvs.2026.1269

Abstract

An effectively immunized parent flock forms the foundation for the proper development of healthy chicks, largely due to the mechanism of vertical transfer of maternal antibodies (MatAb), which provides passive immunity during the early life stages of the chicks. The aim of this study was to evaluate the influence of the age of the Ross 308 parent flock on antibody levels in the serum of the hens and their chicks during the same period with regard to Infectious Bursal Disease (IBD) and Newcastle Disease (ND), as well as to analyses the transfer of antibodies from the hens to their offspring. The study was conducted on a farm with 6500 hens. Blood samples for serological analysis were randomly collected from 84 hens of a single flock and 84 one-day-old chicks hatched from eggs laid by this flock at 30, 40, 50, and 60 weeks of age. In the laboratory, antibody levels in the hens’ blood serum against Newcastle disease virus (NDV) and infectious bursal disease virus (IBDV) were determined using the ELISA test. At the same time, maternal antibody titers (MatAb) in chicks against the same pathogens were measured. The percentage (%) of maternal antibody transfer to the offspring was then assessed. The study demonstrated the impact of parent flock age on antibody levels against the tested pathogens, expressed as geometric mean titers (GMT). During the laying period, GMT values for antibodies against NDV increased with flock age. The highest values were observed at the end of the reproductive period (GMT₆₀=20456), and the lowest at the beginning (GMT₃₀=12631). An opposite trend was observed for IBDV antibodies, whose levels decreased with increasing hen age. The highest values (GMT₃₀=10759) occurred at the beginning of the laying period, and the lowest at its end (GMT₆₀=7421). The highest vertical antibody transfer to offspring was observed for IBDV antibodies (97.7%) at 40 weeks of age, while the lowest was for NDV antibodies (59.7%) at 60 weeks of age. The analysis of results showed significant variation in antibody levels in hen serum during the laying period, as well as in the amount of maternal antibodies transferred to offspring. The obtained data suggest that the effectiveness of passive immunity transfer to chicks is closely related to both the age of the parent flock and the nature of the pathogen targeted by vaccination.

References

Ahmed Z, Akhter S (2003) Role of maternal antibodies in protection against infectious bursal disease in commercial broilers. Int J Poult Sci 2: 251-255.

Alexander DJ (2000) Newcastle disease and other avian paramyxoviruses. Rev Sci Tech 19: 443-462.

Ali MZ, Hasan B (2018) Follow up of maternally derived antibodies titer against economically important viral diseases of chicken. Poult Sci J 6: 149-154.

Aviagen (2016) Ross parent stock management handbook. Huntsville, pp 1-188. Available online: https://www.coursehero.

com/file/39101161/Ross308-PS-PO-EN-2016pdf/

Chrząstek K, Woźniak A, Wieliczko A (2011) Maternal antibodies in birds. Med Weter 67: 250-253.

Chung ELT, Kamalludin MH, Jesse FF, Reduan MF, Ling LW, Mahzan N, Henipah NN, Loh TC, Idrus Z (2020) Health Performance and Blood Profile Changes in Commercial Broilers Supplemented with Dietary Monocalcium Phosphate. Comp Clin Pathol 29: 573-579.

Deka P, Das S, Deka P (2020) Influence of maternal antibody on the efficacy of Newcastle disease vaccination in broilers. Curr J Appl Sci Technol 39: 108-114.

Eidson CS, Gelb J, Villegas P, Page RK, Lukert PD, Kleven SH (1980) Comparison of inactivated and live infectious bursal disease virus vaccines in White Leghorn breeder flock. Poult Sci 59: 2708-2716.

Gharaibeh S, Mahmoud K (2013) Decay of maternal antibodies in broiler chickens. Poult Sci 92: 2333-2336.

Hamal KR, Burgess SC, Pevzner IY, Erf GF (2006) Maternal antibody transfer from dams to their egg yolks, egg whites, and chicks in meat lines of chickens. Poult Sci 85: 1364-1372.

Higgins DA (1975) Physical and chemical properties of fowl immunoglobulins. Vet Bull 45: 139-154.

Kitaguchi K, Osada K, Horio F, Murai A (2008) Exclusion of polymeric immunoglobulins and selective immunoglobulin Y transport that recognizes its Fc region in avian ovarian follicles. Vet Immunol Immunopathol 121: 290-299.

Kowalczyk J, Śmiałek M, Tykałowski B, Dziewulska D, Stenzel T, Koncicki A (2019) Field evaluation of maternal antibody transfer from breeder turkey hens to egg yolks, egg whites, and poults. Poult Sci 98: 3150-3157.

Kowalczyk K, Daiss J, Halpern J, Roth TF (1985) Quantitation of maternal–fetal IgG transport in the chicken. Immunol 54: 755-762.

Leandro NM, Ali R, Koci M, Moraes V, Eusebio-Balcazar PE, Jornigan J, Malheiros RD, Wineland MJ, Brake J, Oviedo-Rondón EO (2011) Maternal antibody transfer to broiler progeny varies among strains and is affected by grain source and cage density. Poult Sci 90: 2730-2739.

Leslie GA, Clem LW (1969) Phylogeny of immunoglobulin structure and function. III. Immunoglobulins of the chicken. J Exp Med 130: 1337-1352.

Müller H, Mundt E, Eterradossi N, Islam MR (2012) Current status of vaccines against infectious bursal disease. Avian Pathol 41: 133-139.

Murai A (2013) Maternal transfer of immunoglobulins into egg yolks of birds. J Poult Sci 50: 185-193.

Murai A, Hamano T, Kakiuchi M, Kobayashi M, Horio F (2020) Evaluation of a receptor gene responsible for maternal blood IgY transfer into egg yolks using bursectomized IgY-depleted chickens. Poult Sci 99: 1914-1920.

Oviedo-Rondón EO, Leandro NM, Ali R, Koci M, Moraes V, Brake J (2013) Broiler breeder feeding programs and trace minerals on mater-nal antibody transfer and broiler humoral immune response. J Appl Poult Res 22: 499-510.

Panth Y (2019) Colibacillosis in poultry: a review. J Agric Nat Res 2: 301-311.

Parker D, de Wit S (2014) Assessment of impact of a novel infectious bursal disease (IBD) vaccination programme in breeders on IBD humoral antibody levels through the laying period. Vet Rec Open 1: e000016.

Rose ME, Orlans E, Buttress N (1974) Immunoglobulin classes in the hen’s egg: their segregation in yolk and white. Eur J Immunol 4: 521-523.

Santos JS, Araújo IC, Lacerda MJ, Andrade MA, Café MB, Leandro NS, Stringhini JH (2022) Effects of broiler breeder age on immune system development of progeny. R Bras Zootec 51: e20210127.

Suardana IB, Widyastuti SK, Pradnyadana IB, Agustina KK (2023) Effect of age and presence of maternal antibodies on success of avian influenza and Newcastle disease vaccinations in broiler. Int J Vet Sci 12: 101-106.

van den Berg TP, Eterradossi N, Toquin D, Meulemans G (2000) Infectious bursal disease (Gumboro disease). Rev Sci Tech 19: 509-543.

Wegner M, Kokoszyński D, Frischke-Krajewska J, Bujko J, Żurek A (2025) Influence of the age of turkey layers on selected serological parameters and the transfer of maternal antibodies to chicks hatched from their eggs. Pol J Vet Sci 28: 17-23.

Downloads

Published

2026-06-15

How to Cite

Wegner, M., and M. Gesek. “The Influence of Ross 308 Breeder Flock Age on Serum Newcastle Disease Virus and Infectious Bursal Disease Virus Antibody Levels and Their Transfer to Offspring”. Polish Journal of Veterinary Sciences, vol. 29, no. 2, June 2026, pp. 263–269, doi:10.24425/pjvs.2026.1269.

Issue

Section

Article

Similar Articles

You may also start an advanced similarity search for this article.