Skip to main content
Acta Veterinaria Scandinavica logoLink to Acta Veterinaria Scandinavica
. 1996 Sep 1;37(3):367–373. doi: 10.1186/BF03548103

A Sperm Midpiece Defect in a Hereford Bull with Variable Semen Quality and Freezability

Mellomstykke-defekt hos spermier fra en Herefordokse med varierende sædkvalitet og spermiefrysbarhet

K Andersen Berg 115,, O Filseth 215, E Engeland 315
PMCID: PMC8064003  PMID: 8996882

Abstract

A midpiece sperm defect with a frequency of 25-35% in ejaculates obtained from a Hereford bull with a 60 d non-retum rate of 76.4% after careful pre- and postfreeze semen selection was studied in light microscope and by transmission electron microscopy. The defect consisted in a folding and coiling of the distal midpiece characterized by disorganization and irregularity of mitochondria surrounding the axial fiber bundle, combined with retraction of doublet fibers and dislocation and fracturing of these elements and the corresponding dense fibers. Based on examination of the sper- matogenic epithelium it was concluded that the alterations in the axial fiber bundle were secondary to those in the mitochondrial sheath. The abnormality appeared to be related to the “Dag-like” defect earlier observed in different breeds.

Keywords: bull sperm, ultrastructure, classification, fertility

Full Text

The Full Text of this article is available as a PDF (642.7 KB).

References

  1. Andrè J. Contribution à la connaissance du chon-driome. Etude de ses modifications ultrastructu-rales pendant la Spermatogenese. J. Ultrastruct. Res. 1962;3:1–185. doi: 10.1016/S0889-1605(62)80002-0. [DOI] [Google Scholar]
  2. Barth AD, Oko RJ. Abnormal Morphology of Bovine Sperm. Iowa: IS Iowa State University Press/Ames; 1989. Defects of the sperm tail; pp. 214–270. [Google Scholar]
  3. Blom E. A simple rapid staining method for differentiation between live and dead sperm cells by means of eosin and nigrosin. Nord. Vet. Med. 1950;2:58–61. [Google Scholar]
  4. Blom E. A new sterilizing and heridity defect (the “Dag” defect) located in the bull sperm tail. Nature. 1966;209:739–740. doi: 10.1038/209739a0. [DOI] [PubMed] [Google Scholar]
  5. Blom E, Birch-Andersen A. The ultrastructure of a new heriditary sterilizing defect (the “Dag” defect) in the bull sperm tail. Proc. 5. Congr. Fertil. Steril. Stockholm. Excerpta Medica) 1966;133:602–605. [Google Scholar]
  6. Blom E, Wolstrup C. Zink as a possible causal factor in the sterilizing sperm tail defect, the “Dag” defect, in Jersey bulls. Nord. Vet. Med. 1976;28:515–518. [PubMed] [Google Scholar]
  7. Burgos MH, Vitale-Calpe R, Aoki A. Fine structure of the testis and its functional significance. The Testis. 1970;I:551–649. [Google Scholar]
  8. Commings DE, Okada TA. The chromatoid body in mouse spermatogenesis: Evidence that it may be formed by extrusion of nucleolar components. J. Ultrastruct. Res. 1972;39:15–23. doi: 10.1016/S0022-5320(72)80003-0. [DOI] [PubMed] [Google Scholar]
  9. Fawcett DW. A comparative view of sperm ultra-structure. Biol. Reprod. 1970;2(Suppl.):90–127. doi: 10.1095/biolreprod2.Supplement_2.90. [DOI] [PubMed] [Google Scholar]
  10. Fulcher KD, Welch JE, Davis CM, O'Brian DA, Eddy EM. Characterization of laminin receptor messenger ribonucleic acid and protein expression in mouse spermatogenic cells. Biol. Reprod. 1993;48:674–682. doi: 10.1095/biolreprod48.3.674. [DOI] [PubMed] [Google Scholar]
  11. Hellmèn E, Plöen L, Settergren I, Nicander L. Middle piece defects of testicular origin in bull sperm. Nord. Vet. Med. 1980;32:423–426. [PubMed] [Google Scholar]
  12. Koefoed-Johnsen HH, Andersen JB, Andresen E, Blom E, Phïlipsen H. The Dag defect of the tail of the bull sperm. Studies on the inheritance and pathogenesis. Theriogenology. 1980;14:471–475. doi: 10.1016/0093-691X(80)90059-X. [DOI] [Google Scholar]
  13. Loir M. Protein and ribonucleic acid metabolism in spermatocytes and spermatids of the ram (Ovis aries). I. Incorporation and fate of 3H-uridine. II. Incorporation and fate of 3H-lysine, 3H-arginine and 35S-cystine. Ann. Biol. Anim. Biochem. Bi-ophys. 1971;12:203–219. doi: 10.1051/rnd:19720202. [DOI] [PubMed] [Google Scholar]
  14. Monesi V. Synthetic activities during spermatogenesis in the mouse. Exptl. Cell Res. 1965;39:197–224. doi: 10.1016/0014-4827(65)90023-6. [DOI] [PubMed] [Google Scholar]
  15. Oko R, Hrudka F. Segemental aplacia of the mitochondrial sheath and sequelae induced by gossy-pol in rat spermatozoa. Biol. Reprod. 1982;26:183–195. doi: 10.1095/biolreprod26.1.183. [DOI] [PubMed] [Google Scholar]
  16. Pallini V, Bacci E. Bull sperm selenium is bound to a structural protein of mitochondria. J. Submi-crosc. Cytol. 1979;11:165–170. [Google Scholar]
  17. Saunders PTK, Millar MR, West AP, Sharpe RM. Mitochondrial cytochrome c oxidase II messenger ribonucleic acid is expressed in pachytene spermatocytes at high levels and in a stage-dependent manner during spermatogenesis in the rat. Biol. Reprod. 1993;48:57–67. doi: 10.1095/biolreprod48.1.57. [DOI] [PubMed] [Google Scholar]
  18. Wallac E, Cooper GW, Calvin Effects of selenium deficiency on the shape and arrangement of rodent mitochondria. Gamete Res. 1983;4:389–399. doi: 10.1002/mrd.1120070410. [DOI] [Google Scholar]
  19. Wenkoff MS. A sperm mid-piece defect of epididymal origin in two Hereford bulls. Theriogenology. 1978;70(4):275–281. doi: 10.1016/0093-691X(78)90105-X. [DOI] [Google Scholar]
  20. Wolley DM. The midpiece of the mouse spermatozoon: Its form and development as seen by surface replication. J. Cell Sci. 1970;6:865–879. doi: 10.1242/jcs.6.3.865. [DOI] [PubMed] [Google Scholar]

Articles from Acta Veterinaria Scandinavica are provided here courtesy of BMC

RESOURCES