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Journal of equine veterinary science2024; 143; 105213; doi: 10.1016/j.jevs.2024.105213

Spermatozoal acrosome dysfunction and its role in stallion subfertility.

Abstract: Cases of stallion subfertility due to acrosome dysfunction have been recognized since the 1990s. While some of these were observed in stallions with reduced sperm motility and morphology, a more severe form has been reported in stallions with normal-to-excellent sperm quality parameters, which is also uniquely observed in individuals of the Thoroughbred registry. These stallions carry a susceptibility genotype (A/A-A A in the gene FKBP6, exon 5) for Impaired Acrosomal Exocytosis (IAE). Current clinical observations from our group have identified a few highly subfertile stallions from other breed registries that also display a lower ability to undergo acrosomal exocytosis (AE) but do not carry the A/A-A/A genotype. This document provides a concise review of the role of acrosome dysfunction as a cause of stallion subfertility, including methods to estimate acrosome function and clinical descriptions of IAE in TB and non-TB stallions.
Publication Date: 2024-10-26 PubMed ID: 39490453DOI: 10.1016/j.jevs.2024.105213Google Scholar: Lookup
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Summary

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Research Overview

  • This research article reviews the role of acrosome dysfunction in causing subfertility in stallions, focusing on a specific genetic susceptibility in Thoroughbred horses and clinical observations of similar issues in other breeds.

Introduction to Acrosome Dysfunction in Stallions

  • Acrosome dysfunction refers to problems with the acrosome, a cap-like structure on the sperm head that is essential for fertilization.
  • Since the 1990s, stallion subfertility linked to acrosome dysfunction has been recognized, with some cases showing reduced sperm motility and abnormal morphology.
  • A more severe form of this dysfunction occurs even in stallions exhibiting normal to excellent sperm quality, notably observed in Thoroughbred stallions.

Genetic Basis of Impaired Acrosomal Exocytosis (IAE)

  • Research has identified a susceptibility genotype (A/A-A/A in the FKBP6 gene, exon 5) that predisposes Thoroughbred stallions to Impaired Acrosomal Exocytosis (IAE).
  • IAE is characterized by the inability of sperm to undergo acrosomal exocytosis, a critical reaction allowing sperm to penetrate the egg.
  • This genetic link suggests that IAE is an inherited cause of subfertility specific to the Thoroughbred breed.

Observations Beyond Thoroughbreds

  • Recent clinical data indicates that some stallions from other breed registries also display poor ability to undergo acrosomal exocytosis.
  • These non-Thoroughbred stallions, however, do not carry the FKBP6 susceptibility genotype.
  • This implies there may be alternative genetic or physiological causes of acrosome dysfunction leading to subfertility in other breeds.

Assessment Methods for Acrosome Function

  • The article reviews current laboratory and clinical techniques used to estimate acrosome function and assess the ability of sperm to undergo acrosomal exocytosis.
  • Testing for acrosome integrity and function is crucial in diagnosing stallion subfertility related to acrosome dysfunction.
  • These methods enable veterinarians and researchers to better understand fertility issues even when routine sperm analysis appears normal.

Clinical Significance and Implications

  • The identification of acrosome dysfunction as a cause of subfertility highlights the importance of functional testing beyond standard sperm quality parameters.
  • For Thoroughbreds, genetic testing for the FKBP6 mutation may help identify carriers and inform breeding decisions to reduce the impact of IAE.
  • Understanding different forms of acrosome dysfunction in other breeds is important for developing breed-specific diagnostic and management strategies.
  • Overall, this research emphasizes the complexity of stallion fertility and encourages more nuanced evaluation protocols.

Cite This Article

APA
Hernández-Avilés C, Ramírez-Agámez L, Varner DD, Raudsepp T, Love CC. (2024). Spermatozoal acrosome dysfunction and its role in stallion subfertility. J Equine Vet Sci, 143, 105213. https://doi.org/10.1016/j.jevs.2024.105213

Publication

ISSN: 0737-0806
NlmUniqueID: 8216840
Country: United States
Language: English
Volume: 143
Pages: 105213
PII: S0737-0806(24)00219-3

Researcher Affiliations

Hernández-Avilés, Camilo
  • Equine Fertility Laboratory, Department of Large Animal Clinical Sciences, College of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, College Station, Texas 77843-4457, United States. Electronic address: chernandez@cvm.tamu.edu.
Ramírez-Agámez, Luisa
  • Equine Fertility Laboratory, Department of Large Animal Clinical Sciences, College of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, College Station, Texas 77843-4457, United States.
Varner, Dickson D
  • Equine Fertility Laboratory, Department of Large Animal Clinical Sciences, College of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, College Station, Texas 77843-4457, United States.
Raudsepp, Terje
  • Molecular Cytogenetics Laboratory, Department of Veterinary Integrative Biosciences, College of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, Texas, United States.
Love, Charles C
  • Equine Fertility Laboratory, Department of Large Animal Clinical Sciences, College of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, College Station, Texas 77843-4457, United States.

MeSH Terms

  • Horses
  • Animals
  • Male
  • Acrosome / pathology
  • Horse Diseases / physiopathology
  • Horse Diseases / pathology
  • Horse Diseases / genetics
  • Infertility, Male / veterinary
  • Infertility, Male / genetics
  • Infertility, Male / pathology
  • Infertility, Male / physiopathology
  • Spermatozoa / pathology
  • Acrosome Reaction

Conflict of Interest Statement

Declaration of competing interest The authors declare that no generative AI or AI-assisted technologies were employed during the writing process of this manuscript. Also, the authors declare no conflict of interest.

Citations

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