Vet World   Vol.14   June-2021  Article-10

Research Article

Veterinary World, 14(6): 1472-1479

https://doi.org/10.14202/vetworld.2021.1472-1479

Allele and genotype frequencies of the SOD1 gene polymorphism associated with canine degenerative myelopathy in Belgian Malinois dogs in Greece

Antonia Mataragka1, John Ikonomopoulos1, Georgios S. Zervas1, Christos D. Vamvakidis2, Nikolaos Tzimotoudis3, Ariadne Loukia Hager-Theodorides4, Maria Gazouli5, and Antonios Kominakis4
1. School of Animal Biosciences, Department of Animal Science, Laboratory of Anatomy and Physiology of Farm Animals, Agricultural University of Athens, Athens, Greece.
2. Hellenic Army Biological Research Center/Veterinary Clinic, Athens, Greece.
3. Hellenic Army Biological Research Center/Laboratory of Microbiology, Athens, Greece.
4. School of Animal Biosciences, Department of Animal Science, Laboratory of Animal Breeding and Husbandry, Agricultural University of Athens, Athens, Greece.
5. School of Medicine, Department of Basic Medical Science, Laboratory of Biology, Kapodistrian University of Athens, Athens, Greece.

Background and Aim: Canine degenerative myelopathy (CDM) is an adult-onset fatal disorder associated with a point mutation of the superoxide dismutase 1 (SOD1) gene (SOD1:c.118G>A). This study aimed to determine the allele and genotype frequencies of this mutation in a group of Belgian Malinois dogs in Greece.

Materials and Methods: Samples (n=72) of whole blood were collected from 72 purebred dogs of the Hellenic Armed Forces; these samples were processed for DNA isolation, polymerase chain reaction, and digestion with the restriction endonuclease AcuI. Sample testing was conducted in compliance with ISO17025 accreditation requirements.

Results: The observed relative genotype frequencies were 71% for the homozygous (GG), 25% for the heterozygous (AG), and 4% for the homozygous mutant (AA) alleles. These frequencies were close to those expected, indicating no significant departure from Hardy–Weinberg equilibrium (HWE, p=0.395). The frequency of heterozygous animals indicates that a high risk of developing CDM in forthcoming generations exists in the tested population because mating among carriers would result in 25% AA progeny. The medical record of the group of study animals indicated selection against leishmaniosis, as applied throughout generations by owners and breeders. The potential association of this selection with the HWE status of the study population was discussed.

Conclusion: The SOD1:c.118G>A mutation was common in the tested group of dogs; thus, they are suitable for a follow-up investigation on the development and progression of CDM. A case-control study on animals with evidence of sensitivity to infectious myelopathy could provide new insights into disease pathogenesis. Keywords: degenerative myelopathy, dogs, genetic analysis, genetic polymorphism, restriction fragment length polymorphism-polymerase chain reaction, SOD1:c.118A.

Keywords: degenerative myelopathy, dogs, genetic analysis, genetic polymorphism, restriction fragment length polymorphism-polymerase chain reaction, SOD1:c.118A.

How to cite this article: Mataragka A, Ikonomopoulos J, Zervas GS, Vamvakidis CD, Tzimotoudis N, Hager-Theodorides AL, Gazouli M, Kominakis A (2021) Allele and genotype frequencies of the SOD1 gene polymorphism associated with canine degenerative myelopathy in Belgian Malinois dogs in Greece, Veterinary World, 14(6): 1472-1479.

Received: 12-11-2020  Accepted: 16-04-2021     Published online: 09-06-2021

Corresponding author: Antonios Kominakis   E-mail: acom@aua.gr

DOI: 10.14202/vetworld.2021.1472-1479

Copyright: Mataragka, et al. This article is an open access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http:// creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.