Morphogenesis of the ostrich (Struthio camelus) trachea and lung in different embryonic and fetal stages

Document Type : Original Article

Authors

1 Department of Basic Sciences, Faculty of Veterinary Medicine, Ferdowsi University of Mashhad, Mashhad, Iran

2 Department of Basic Sciences, Faculty of Veterinary Medicine, Shahid Bahonar University of Kerman, Kerman, Iran

Abstract
The ostrich (Struthio camelus) is an important wild species highlighted in national and international livestock industry. This research was conducted to analyze the development of the ostrich respiratory system during fetal and embryonic stages. A total of 50 fertile ostrich eggs were collected from commercial farms and then incubated at 36.00 - 37.00 ˚C and 25.00 ± 2.00% humidity for 40 days. Sections were taken on days 13, 22, 26, 30, 36, and 42 of incubation from the lung and the cranial, middle, and caudal parts of the neck after decapitation of ostrich embryos and blood drainage. After fixation, processing, blocking, and sectioning, all samples were stained by Hematoxylin and Eosin, Alcian Blue (AB), Van Gieson, and Periodic acid-Schiff (PAS) techniques. It was concluded that the trachea in the 13-day-old embryo and goblet cells (PAS-positive and AB-positive) had incomplete rings of hyaline cartilage and differentiation of mesenchymal to the loose connective tissue. The bronchial stage of the lung was observed in the 22-day-old embryo, pseudoglandular stage in the 26-day-old embryo, and parabrachial and air capillary stage in the 30-day-old embryo. The information obtained from this study will be useful for diagnosing pathologies affecting this vital system and results in improving industrial breeding management.

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  1. Casteleyn C, Cornillie P, Van Cruchten S, et al. Anatomy of the lower respiratory tract in domestic birds, with emphasis on respiration. Anat Histol Embryol 2018; 47(2): 89-99.
  2. Sousa RP, Monteiro HM, Bezerra DD, et al. Morphogenesis of the rhea (Rhea americana) respiratory system in different embryonic and foetal stages. Pesq Vet Bras 2018; 38(1):154-166.
  3. Bellairs R, Osmond M. Atlas of chick development. 2nd London, UK: Elsevier Academy Press; 2005; 15.
  4. Sakiyama J, Yamagishi A, Kuroiwa A. Tbx4-Fgf10 system controls lung bud formation during chicken embryonic development. Development 2003; 130(7): 1225-1234.
  5. Kang H, Yan M, Yu Q, et al. Characteristics of nasal-associated lymphoid tissue (NALT) and nasal absorption capacity in chicken. PLoS One 2013; 8(12): e84097. doi: 10.1371/journal.pone.0084097.
  6. López J, Cuesta N, Burrel MA. Brush-like cells within bronchial epithelia of chicken lung (Gallus gallus). Histol Histopathol 2000; 15(2): 487-491.
  7. Maina JN. The design of the avian respiratory system: development, morphology and function. J Ornitholo 2015; 156 (Suppl 1): 41-63.
  8. Abidu-Figueiredo M, Santos CM, de Castro Bath FV, et al. Morphological aspects of the ostrich larynx (Struthio camelus) [Portuguese]. Rev Bras Vet Med 2012; 34(3): 202-205.
  9. Yildiz H, Bahadir A, Akkoç A. A study on the morphological structure of syrinx in ostriches (Struthio camelus). Anat Histol Embryol 2003; 32(3): 187-191.
  10. Brand Z, Cloete SW, Malecki IA, Brown CR. Embryonic development in the ostrich (Struthio camelus) during the first 7 days of artificial incubation. BR J Poult Sci 2014; 2; 55(1):68-75.
  11. Smith JH, Meier JL, Lampke C, et al. Microscopic and ultrastructural anatomy of the trachea and bronchi of Melopsittacus undulatus (Aves, Psittaciformes). Zoomorphology 1987; 107:1-10.
  12. Cevik‐Demirkan A, Haziroğlu RM, Kürtül I. Gross morphological and histological features of larynx, trachea and syrinx in Japanese quail. Anat Histol Embryol 2007; 36(3): 215-219.
  13. Khaksar Z, Tavakol Kookhdan E, Parto P. A study on anatomy and histological structure of larynx in adult male and female turkeys. World J Zool 2012; 7(3): 45-250.
  14. Runciman S, Seymour RS, Baudinette RV, et al. An allometric study of lung morphology during development in the Australian pelican, Pelicanus conspicillatus, from embryo to adult. J Anat 2005; 207(4): 365-380.
  15. Tzou D, W Spurlin J 3rd, Pavlovich AL, et al. Morphogenesis and morphometric scaling of lung airway development follows phylogeny in chicken, quail, and duck embryos. EvoDevo 2016; 7:12. doi: 10.1186/s13227-016-0049-3.
  16. Makanya AN. Development of the airways and the vasculature in the lungs of birds. In: Maina J (Ed). The biology of the avian respiratory system. Berlin, Germany: Springer Cham; 2017:147-178.
  17. Makanya AN, Hlushchuk R, Djonov V. The pulmonary blood–gas barrier in the avian embryo: inauguration, development and refinement. Respir Physiol Neurobiol 2011; 178(1): 30-38.
  18. Walsh C, McLelland J. The development of the epithelium and its innervation in the avian extra-pulmonary respiratory tract. J Anat 1978; 125(Pt 1): 171-182.
  19. Rock JR, Hogan BL. Epithelial progenitor cells in lung development, maintenance, repair, and disease. Annu Rev Cell Dev Biol 2011; 27: 493-512.
  20. Frank T, Walter I, Probst A, et al. Histological aspects of the syrinx of the male mallard (Anas platyrhynchos). Anat Histol Embryol 2006; 35(6): 396-401.
  21. Perl AK, Whitsett JA. Molecular mechanisms controlling lung morphogenesis: Clin Genet 1999; 56(1): 14-27.
  22. Makanya AN, Koller T, Hlushchuk R, et al. Pre-hatch lung development in the ostrich. Respir Physiol Neurobiol 2012; 180(2-3): 183-192.
Volume 15, Issue 6
June 2024
Pages 297-301

  • Receive Date 22 August 2023
  • Revise Date 13 November 2023
  • Accept Date 02 December 2023