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Equine veterinary journal2008; 40(6); 590-591; doi: 10.2746/042516408x333001

Frequency of the severe combined immunodeficiency disease gene among horses in Morocco.

Abstract: Severe combined immunodeficiency disease (SCID) of horses is an autosomal, recessive hereditary disease occurring among Arabian or crossbred Arabian horses. The genetic defect responsible was previously identified as a 5-base pair deletion in the gene encoding the catalytic subunit of the DNA dependant protein kinase (DNA-PKcs). This study was carried out to determine the frequency of SCID and identify horses carrying the gene for SCID among Arabian and Arabian crossbred stallions and mares in Morocco using a DNA-based test. Twenty-one horses were SCID carriers: 14 (7%) Arabians, 6 (4%) Arab-Barbs and one (33%) Anglo-Arab. After analysing their genealogy, 3 imported stallions were identified that disseminated the mutant gene of DNA-PKcs in Morocco.
Publication Date: 2008-11-26 PubMed ID: 19031514DOI: 10.2746/042516408x333001Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research paper is about a study conducted to determine the frequency of severe combined immunodeficiency disease (SCID) in Arabian and crossbreed Arabian horses in Morocco, using a DNA-based test.

Severe Combined Immunodeficiency Disease in Horses

  • Severe Combined Immunodeficiency Disease (SCID) is a hereditary disease that primarily affects Arabian, or Arabian-crossbred horses. It is an autosomal, recessive disease implying that a horse needs to inherit the defective gene from both parents to develop the disease.
  • The disease is caused by a mutation in the DNA-PKcs gene, a gene that encodes the catalytic subunit of DNA-dependent protein kinase. Specifically, the mutation responsible for SCID in horses is a 5-base pair deletion in the DNA-PKcs gene.
  • SCID diagnosed horses have highly compromised immune systems, making them susceptible to various infections.

Objective and Methodology of the Study

  • The primary objective of this study was to determine the incidence or frequency of the SCID gene in Arabian and Arabian crossbred stallions and mares in Morocco.
  • The researchers utilised a DNA-based test to identify horses carrying the SCID gene.

Findings of the Study

  • The results of the study reveal that out of a total number of horses tested, twenty-one were carriers of the SCID gene. The breakdown includes:
    1. 14 (7%) Arabian horses,
    2. 6 (4%) Arabian-Barb horses (a crossbred), and
    3. 1 (33%) Anglo-Arab horse (another crossbred).
  • The researchers were also able to trace the spread of the SCID gene to three imported stallions. These stallions were identified as the original source of the mutants in the Moroccan horse population, having disseminated the mutated DNA-PKcs gene.

Significance of the Study

  • This research provides valuable insights into the prevalence of SCID in the horse population in Morocco.
  • By identifying the carriers of this gene, it could aid in preventing the spread of this disease by controlling the breeding of horses carrying the SCID gene.
  • The identification of imported stallions as the source of the mutant gene also informs import control and breeding policies to prevent the spread of the disease.

Cite This Article

APA
Piro M, Benjouad A, Tligui NS, El Allali K, El Kohen M, Nabich A, Ouragh L. (2008). Frequency of the severe combined immunodeficiency disease gene among horses in Morocco. Equine Vet J, 40(6), 590-591. https://doi.org/10.2746/042516408x333001

Publication

ISSN: 0425-1644
NlmUniqueID: 0173320
Country: United States
Language: English
Volume: 40
Issue: 6
Pages: 590-591

Researcher Affiliations

Piro, M
  • Veterinary Genetics Laboratory, Hassan II Institute of Agronomy and Veterinary Medicine, Department of Medicine Surgery and Animal Breeding, 10101 Rabat, Morocco.
Benjouad, A
    Tligui, N S
      El Allali, K
        El Kohen, M
          Nabich, A
            Ouragh, L

              MeSH Terms

              • Animals
              • Breeding
              • DNA-Activated Protein Kinase
              • Female
              • Gene Frequency / genetics
              • Horse Diseases / diagnosis
              • Horse Diseases / genetics
              • Horses
              • Male
              • Morocco / epidemiology
              • Polymerase Chain Reaction / veterinary
              • Protein Serine-Threonine Kinases / genetics
              • Severe Combined Immunodeficiency / diagnosis
              • Severe Combined Immunodeficiency / genetics
              • Severe Combined Immunodeficiency / veterinary

              Citations

              This article has been cited 3 times.
              1. Kassymbekova SN, Bimenova ZZ, Iskhan KZ, Sobiech P, Jastrzebski JP, Brym P, Babis W, Kalykova AS, Otebayev ZM, Kabylbekova DI, Baneh H, Romanov MN. Uncovering Genetic Diversity and Adaptive Candidate Genes in the Mugalzhar Horse Breed Using Whole-Genome Sequencing Data. Animals (Basel) 2025 Sep 11;15(18).
                doi: 10.3390/ani15182667pubmed: 41007912google scholar: lookup
              2. Ayad A, Almarzook S, Besseboua O, Aissanou S, Piórkowska K, Musiał AD, Stefaniuk-Szmukier M, Ropka-Molik K. Investigation of Cerebellar Abiotrophy (CA), Lavender Foal Syndrome (LFS), and Severe Combined Immunodeficiency (SCID) Variants in a Cohort of Three MENA Region Horse Breeds. Genes (Basel) 2021 Nov 26;12(12).
                doi: 10.3390/genes12121893pubmed: 34946842google scholar: lookup
              3. Al Abri MA, Holl HM, Kalla SE, Sutter NB, Brooks SA. Whole genome detection of sequence and structural polymorphism in six diverse horses. PLoS One 2020;15(4):e0230899.
                doi: 10.1371/journal.pone.0230899pubmed: 32271776google scholar: lookup