ISSN: 2536-7099
Model: Open Access/Peer Reviewed
DOI: 10.31248/JASVM
Start Year: 2016
Email: jasvm@integrityresjournals.org
https://doi.org/10.31248/JASVM2025.575 | Article Number: E478FD346 | Vol.10 (4) - August 2025
Received Date: 12 June 2025 | Accepted Date: 07 August 2025 | Published Date: 30 August 2025
Authors: Nnadozie, O.* , Nwaogu, I. C. , Ibe, C. S. and Ikpegbu, E.
Keywords: development, indigenous chicken., morphology, post-hatch, pre-hatch, spleen.
The avian spleen is a primary peripheral lymphoid organ located in the region dorsal to the gonad, ventral to the liver and lateral to the stomach, just opposite the dorsal surface of the right hepatic lobe. It plays both lymphopoietic and hematopoietic roles, depending on the respective amounts of white pulp and red pulp elements in the parenchyma. The pre- and post-hatch development of the spleen of native chicken ecotype predominant in the south eastern region of Nigeria was studied from embryonic incubation day (EID) 10 to day (D) 42 post hatch using gross anatomical and histological techniques to detect age-related developmental changes associated with the spleen and the relative time of establishment of the basic immunological structures of the spleen. The embryos were harvested from the eggs at different embryonic ages for the pre-hatch studies. The spleen was collected through a ventral abdominal incision in both embryos and post-hatch chicks, weighed and fixed in neutral-buffered formalin. The fixed tissues were routinely processed and stained with haematoxylin and eosin (H&E) for histological studies. The mean weight of the spleen increased significantly (p < 0.05) between D 14, 28 and 42, while the relative weight varied significantly between D 14 and 28. The spleen was bean-shaped at EID 10 and throughout the post-hatch periods, but it became triangular at EID 14. The colour was relatively red in both embryos and post-hatch chicks. At EID 10, the parenchyma was undifferentiated into white and red pulp regions, but splenic sinusoids had developed. At EID 14, lymphocytes had infiltrated into the parenchyma and white and red pulp zones fairly distinct. Apparent white and red pulp regions appeared at EID 18, but were more prominent at hatch (D 0). Ellipsoids and periarteriolar lymphoid sheath equally developed at hatch. By D 7, the arterial wall and the capsule increased in thickness. The parenchyma appeared to be dominated by the white pulp elements between D 0 and D 42. There was also a progressive increase in lymphocyte densities during the post-hatch periods, but splenic nodules only developed at D 42. The development of the spleen as a functional peripheral lymphoid organ in native chickens of Nigeria occurred in the embryos but progresses after hatch, and the dominance of the parenchyma by the white pulp during the embryonic and early post-hatch periods of development emphasised lymphopoietic responsibility of the spleen in Nigerian native chicken.
| Alboghobeish, N. and Mayahi, M. (2003). Developmental study of lymphoid tissue of bursa of Fabricius in local chicken. The 11th Symposium of World Association of Veterinary Laboratory Diagnosticians and the World Organisation for Animal Health Seminar on Biotechnology, Nov. 9-13. | ||||
| Ciriaco, E., Píñera, P. P., Díaz‐Esnal, B., & Laurà, R. (2003). Age‐related changes in the avian primary lymphoid organs (thymus and bursa of Fabricius). Microscopy research and technique, 62(6), 482-487. https://doi.org/10.1002/jemt.10416 |
||||
| Davison, F., Kaspers, B., & Schat, K. A. (2008). Avian immunology. Academic Press is an imprint of Elsevier, Cambridge, MA. | ||||
| Dieter, M. P., & Breitenbach, R. P. (1968). The growth of chicken lymphoid organs, testes, and adrenals in relation to the oxidation state and concentration of adrenal and lymphoid organ vitamin C. Poultry Science, 47(5), 1463-1469. https://doi.org/10.3382/ps.0471463 |
||||
| Hodges, R. D. (1974). The histology of the fowl. Academic Press, London. | ||||
| Indu, V. R., Chungath, J. J., Harshan, K. R., & Ashok, N. (2005). Morphology and histochemistry of the bursa of Fabricius in White Pekin ducks. Indian Journal of Animal Sciences, 75(6), 637-639. | ||||
| Islam, M. N., Khan, M. Z. I., Jahan, M. R., Fujinaga, R., Yanai, A., Kokubu, K., & Shinoda, K. (2012). Histomorphological study on prenatal development of the lymphoid organs of native chickens of Bangladesh. Pakistan Veterinary Journal, 32(2), 175-178. | ||||
| John, J. L. (1994). The avian spleen: a neglected organ. The Quarterly Review of Biology, 69(3), 327-351. https://doi.org/10.1086/418649 |
||||
| Kasai, K., Nakayama, A., Ohbayashi, M., Nakagawa, A., Ito, M., Saga, S., & Asai, J. (1995). Immunohistochemical characteristics of chicken spleen ellipsoids using newly established monoclonal antibodies. Cell and tissue research, 281(1), 135-141. https://doi.org/10.1007/BF00307967 |
||||
| Lıman, N., & Bayram, G. K. (2011). Structure of the quail (Coturnix coturnix japonica) spleen during pre-and post-hatching periods. Revue de Médecine Vétérinaire, 162(1), 25-33 | ||||
| Mast, J., & Goddeeris, B. M. (1997). CD57, a marker for B-cell activation and splenic ellipsoid-associated reticular cells of the chicken. Cell and tissue research, 291(1), 107-115. https://doi.org/10.1007/s004410050984 |
||||
| Moges, F., Mellesse, A., & Dessie, T. (2010). Assessment of village chicken production system and evaluation of the productive and reproductive performance of local chicken ecotype in Bure district, North West Ethiopia. African Journal of Agricultural Research, 5(13), 1739-1748. | ||||
| Moreki, J. C., Dikeme, R., & Poroga, B. (2010). The role of village poultry in food security and HIV/AIDS mitigation in Chobe District of Botswana. Livestock Research for Rural Development, 22(3), 1-7. | ||||
| Negassa, D., Melesse, A., & Banerjee, S. (2014). Phenotypic characterisation of indigenous chicken populations in Southeastern Oromia Regional State of Ethiopia. Animal Genetic Resources, 55, 101-113. https://doi.org/10.1017/S2078633614000319 |
||||
| Ogata, K., Sugimura, M., & Kudo, N. (1977). Developmental studies on embryonic and posthatching spleens in chickens with special reference to development of white pulp. Japanese Journal of Veterinary Research, 25(3-4), 83-92. | ||||
| Olah, I., & Vervelde, L. (2008). Structure of the avian lymphoid system. In: Davison, F., Kaspers, B., & Schat, K. A. (eds.). Avian immunology (pp. 13-35). Academic Press-Elsevier. https://doi.org/10.1016/B978-012370634-8.50005-6 |
||||
| Onyeanusi, B. I. (2006). The Guinea Fowl Spleen at Embryonic and Post‐Hatch Periods. Anatomia, Histologia, Embryologia, 35(3), 140-143. https://doi.org/10.1111/j.1439-0264.2005.00641.x |
||||
| Onyeanusi, B. I., & Onyeanusi, J. C. (1990). Growth of the lymphoid organs in the indigenous guinea fowl of Nigeria. Tropical Veterinarian, 8(1-2), 9-15. | ||||
| Oznurlu, Y., Celik, I., Telatar, T., & Sur, E. (2010). Histochemical and histological evaluations of the effects of high incubation temperature on embryonic development of thymus and bursa of Fabricius in broiler chickens. British Poultry Science, 51(1), 43-51. https://doi.org/10.1080/00071660903575558 |
||||
| Payne, I. N. (1971). Lymphoid system (A review). In: Bell, D. J., & Freeman, B. M. (eds.). physiology and biochemistry of the domestic fowl (Vol. 2: 985-1037). Academic Press, New York. | ||||
| Ratcliffe, M. J. H. (1989). Development of the avian B-lymphocytes lineage. Critical Review on Poultry Science, 2, 207-234. | ||||
| Silverstein, A. M. (2001). The lymphocyte in immunology: from James B. Murphy to James L. Gowans. nature immunology, 2(7), 569-571. https://doi.org/10.1038/89706 |
||||
| Smith, K. G., & Hunt, J. L. (2004). On the use of spleen mass as a measure of avian immune system strength. Oecologia, 138(1), 28-31. https://doi.org/10.1007/s00442-003-1409-y |
||||
| Yoshimura, Y., Tsuyuki, C., Subedi, K., Kaiya, H., Sugino, T., & Isobe, N. (2009). Identification of ghrelin in fertilized eggs of chicken. The Journal of Poultry Science, 46(3), 257-259. https://doi.org/10.2141/jpsa.46.257 |
||||