On-line version ISSN 2224-9435
J. S. Afr. Vet. Assoc. vol.84 n.1 Cape Town Jan. 2013
Gareth E. ZeilerI; Henriette van der ZwanII; Marinda C. OosthuizenIII
IDepartment of Companion Animal Clinical Studies, University of Pretoria, South Africa
IIInqaba Biotec, Pretoria, South Africa
IIIDepartment of Veterinary Tropical Diseases, University of Pretoria, South Africa
Canine degenerative myelopathy (DM) is a progressive disease process that is diagnosed late in life and mainly affects the pelvic limbs. Factors that make an ante-mortem definitive diagnosis of DM include: an insidious onset and clinical manifestation that mimics other disease processes of the pelvic limbs (hip dysplasia, cranial cruciate ligament rupture, etc.) or there may even be concurrent disease processes, old-age onset and lack of reliable diagnostic methods. Until recently, South African dog owners had to submit samples to laboratories overseas for genetic testing in order to confirm an affected dog (homozygous A/A) and to aid in the ante-mortem diagnosis of DM. Only affected dogs have been confirmed to manifest the clinical signs of DM. This study aimed to verify whether genetic testing by a local genetic laboratory was possible in order to detect a missense mutation of the superoxide dismutase gene (SOD1) that is implicated in causing the clinical signs of DM. The study also aimed to detect and map the inheritance of this disease process in a local Boxer dog population where the pedigree of the sampled population was known. Venous blood collected from Boxer dogs using a simple random sampling technique. The samples were genotyped for the SOD1:c.118G>A polymorphism. Carrier and affected Boxer dogs were detected. A pedigree that demonstrated the significance of inheriting a carrier or affected state in the population was mapped. The present study concludes that genotyping of the missense mutation in Boxer dogs is possible in South Africa. There are carrier and affected Boxer dogs in the local population, making DM a plausible diagnosis in aged dogs presenting with pelvic limb pathology.
Clinical and pathological findings of degenerative myelopathy (DM) were first described in the German Shepherd dog by Averill (1973). In the earlier descriptions of this disease process, canine DM has also been called chronic degenerative radiculomyelopathy (Griffiths & Duncan 1975), German Shepherd dog myelopathy (Braund & Vandevelde 1978) and progressive myelopathy (Waxman, Clemmons & Hinrichs 1980). Early investigation of the clinical manifestations of DM, which were most often recognised in the German Shepherd dog, suggested an inherent breed genetic predisposition (Braund & Vandevelde 1978). Investigation into leukocyte behaviour suggested an autoimmune-based aetiology (Waxman, Clemmons & Hinrichs 1980). Hereditary factors were suspected when DM was described in closely related Siberian Husky dogs (Bichsel et al. 1983). To date, DM has been diagnosed in many different dog breeds (Coates & Wininger 2010). The five most frequently diagnosed dog breeds with DM are German Shepherd dogs, Pembroke Welsh corgis, Boxer dogs, Rhodesian ridgebacks and Chesapeake Bay retrievers (Awano et al. 2009; Coates et al. 2007).
Characteristic clinical presentation of DM includes: an insidious, progressive onset of asymmetric upper motor neuron (UMN) paraparesis; general proprioceptive pelvic limb ataxia; and lack of paraspinal hyperaesthesia (Awano et al. 2009; Coates et al. 2007; Coates & Wininger 2010). These clinical signs are typical of the early stages of DM and may also include worn nails, spinal reflexes consistent with UMN paresis localised in the T3 to L3 spinal cord segment (Averill 1973), inconsistent patella reflex (normal, hyporeflexia, hyperreflexia) and normal withdrawal reflexes that may demonstrate crossed extension, which is suggestive of a chronic UMN dysfunction.
Owners often elect euthanasia when the clinical signs progress to a non-ambulatory paraparesis (Awano et al. 2009; Coates & Wininger 2010). Clinical signs will progress in the late stage of DM and include lower motor neuron paraplegia that may ascend to the thoracic limbs (Averill 1973; Awano et al. 2009; Coates et al. 2007; Coates & Wininger 2010). Flaccid tetraplegia, possible involvement of the cranial nerves presenting as swallowing difficulties and inability to bark, urinary and faecal incontinence, and muscle mass loss may occur in the very advanced stages (Averill 1973; Awano et al. 2009; Coates et al. 2007; Coates & Wininger 2010). The mean age of onset and mean duration of clinical signs in the Boxer dog are 9.3 years and 11.2 months respectively (Coates & Wininger 2010). Mean age of death in the Boxer dog is 10.3 years (Coates & Wininger 2010).
Advances in molecular genetics have progressed to genome-wide association mapping of DM using the Canine Genome (GeneChip Canine Genome 2.0 Array; Affymetrix, USA) (Awano et al. 2009). The strongest association was detected in the chromosome of Canis familiaris 31 (CFA31), where a mutation of the gene encoding superoxide dismutase 1 (SOD1) was mapped and localised to a 5-SNP (single nucleotide polymorphism) haplotype. The area of the genome contains the E40K missense mutation that predicts a G to A transition in exon 2, corresponding to nucleotide 118 of the complementary DNA (cDNA). This area is thought to be responsible for encoding a defect in the SOD1 amino acid chain (Awano et al. 2009). The defect is where a glutamic acid to lysine missense mutation at amino acid 40 (Coates & Wininger 2010) is predicted. Dogs may be genotyped into three different categories, based on the genotypic expression of the SOD1:c.118 allele, namely: unaffected, carrier, or at-risk or affected (Awano et al. 2009; Coates et al. 2007; Coates & Wininger 2010).
The present study was aimed at detecting carrier and/or affected Boxer dogs of DM in the South African population using a SOD1:c.118G>A genetic test that had recently been developed in South Africa. This article also discusses the potential clinical relevance within a South African context.
Materials and Methods
The prospective, owner-consented, blind, observational study was approved by the Animal Use and Care Committee of the University of Pretoria (Protocol V005-13).
A targeted sample size of 50 Boxer dogs was genotyped for the SOD1:c.118G>A polymorphism. No exclusion criteria on age, sex or pedigree were enforced. A history of prior hind limb pathology and gait abnormalities was obtained to determine possible phenotypic expression of DM. A simple random sampling technique was used where the owners were made aware of the study 2 weeks prior to the sample collection and were allowed to enrol their dog or dogs at their own will on the day of sample collection. It was prohibited to encourage, promote or entice the owners to participate in the study.
Sample collection and storage
Boxer dogs were sampled at two dog show days hosted by clubs affiliated with the Federation of Boxer Clubs of Southern Africa (FBCSA). An owner-signed consent form and dog pedigree registration certificate showing the last three generations was required before sampling. Venous blood (2 mL) was aseptically collected from either the left or right cephalic vein using a syringe and needle. The collected sample was transferred to a vacuumed Ethylenediaminetetraacetic acid (EDTA) collection tube and stored on ice in a cooler box. Upon return to the University, the samples were stored overnight in a refrigerator before being transported on ice in a cooler box to the genetic testing laboratory. The number of dogs participating in the two shows and an estimated Boxer dog population size based on the FBSCA database were determined.
Genotyping of the superoxide dismutase gene:c.118 allele
The genetic testing laboratory (Inqaba Biotec, South Africa) developed an in-house DM test, which was based on literature published on the canine SOD1 gene (Awano et al. 2009). The genetic testing laboratory synthesised their own oligonucleotides used for testing, based on the sequences published by Awano et al. (2009). DNA was extracted and purified using a kit (Zymo Research Quick-gDNA MicroPrep kit, Zymo Research Corporation [USA] 17062 Murphy Ave. Irvine, CA 92614). A polymerase chain reaction (PCR) amplification was carried out on a cycler (ABI GeneAmp PCR system 9700 thermal cycler; Applied Biosystems) to amplify the gene of interest. The cycle conditions are given in Table 1. Thereafter, the amplicons were sequenced on an analyser (ABI PRIS 3130 Genetic Analyzer; Applied Biosystems) to determine the nucleotide sequence of the gene. Boxer dogs were genotyped into three different categories, namely: clear or unaffected (homozygous G/G), carrier (heterozygous A/G), and at-risk or affected (homozygous A/A) based on the genotypic expression of the SOD1:c.118 allele. Where applicable, the registration certificate information of the pedigree was used to describe the hereditary nature of the mutation in the SOD1 gene in the sampled population.
The age of the sampled Boxer dog population was described as median (maximum-minimum) in years. A spreadsheet software package (Microsoft Office Excel 2007; Microsoft Corporation USA) was used to organise and calculate information from the data collected. Point prevalence of dogs genotyped as affected for the SOD1 mutation in the FBCSA Boxer dog population was calculated as follows: number of dogs genotyped as being affected when sampled on the show day divided by the total number of dogs participating in the show on the sample day; this number was then converted into a percentage. Overall prevalence of affected genotyped dogs was calculated as follows: known number of affected genotyped Boxer dogs divided by the estimated FBCSA dog population. This number was then converted into a percentage.
A total of 52 (29 female, 23 male) Boxer dogs were tested. The sample population had a median median age of 2.7 (maximum of 9.7; minimum of 0.53) years. The numbers of clear, carrier and affected Boxer dogs are summarised in Table 2. The percentages of dogs sampled per show were 72.7% and 68.3% for show day 1 and show day 2 respectively.
The hereditary nature of DM was detected in one line of Boxer dogs that were sampled (Figure 1). The progeny of the only affected dog genotyped during the data collection were subsequently tested and an additional five affected dogs were detected. The owner of the affected dog did indicate a history of pelvic limb abnormalities that had not been definitively diagnosed as DM, instead cranial cruciate ligament injury was suspected on cursory clinical examination.
Point prevalence of Boxer dogs genotyped as affected were 3.03% and 0.00% for show day 1 and show day 2 respectively. Based on current database information, the estimated FBCSA population is 2650 Boxer dogs. Current overall prevalence of affected Boxer dogs within the FBCSA dog population is estimated ([1 affected + 5 affected progeny/2650] x 100) at 0.23%.
The present study determined that the recently available genetic test for canine DM in South Africa was able to genotype the SOD1:c.118 allele in a Boxer dog population. Clear, carrier and affected Boxer dogs were identified despite none of them demonstrating typical clinical signs of DM on examination. Enquiring about past pelvic limb or gait abnormalities suggested acute injuries to the stifle joint, with cranial cruciate ligament injury as the most common historical finding.
The DM associated SOD1:c118A homozygous (affected) allele has been identified in no less than 91 different dog breeds (Coates & Wininger 2010). Despite identifying the genotypic variation that causes a missense mutation in the gene coding for SOD1, it remains unclear as to whether affected animals will express phenotypic traits of DM during their lifetime (Awano et al. 2009; Coates et al. 2007). Previous studies have found that affected dogs may not exhibit clinical signs of DM, which suggests an incomplete penetrance. The incomplete penetrance may be due to modifier loci, environmental factors, and/or death of affected dogs due to other causes before the clinical signs of DM manifest (Awano et al. 2009). Thus, the current literature suggests that an affected dog is at risk of developing clinical signs of DM and not that the dog will develop clinical signs of DM owing to incomplete penetrance (Awano et al. 2009; Coates et al. 2007; Coates & Wininger 2010).
The characteristic clinical signs associated with DM are attributed to the histopathological changes in the spinal cord thought to be due to the malformation of the SOD1 protein (Awano et al. 2009; Barclay & Haines 1994; Clemmons 1992; Coates et al. 2007; Coates & Wininger 2010; Cork et al. 1987; Johnston et al. 2000; Miller et al. 2009; Ogawa et al. 2011; Shelton et al. 2012; Tsai et al. 2012; Wininger et al. 2011). The SOD1 protein functions as a free radical scavenger within the central nervous system (Awano et al. 2009; Coates & Wininger 2010). The missense mutation causes the SOD1 protein to fold incorrectly, which reduces its net negative charge. This is thought to be the cause of increased intracellular accumulation and aggregation of this protein due to either reduced repulsive Coulombic forces or increased anionic membrane surface interaction (Coates & Wininger 2010). These insoluble intracellular SOD1 aggregates are thought to either alter intracellular function or alter the enzyme substrate specificity, leading to toxic by-product production that causes the neurodegenerative changes associated with the disease (Coates & Wininger 2010). These characteristic histopathological lesions are considered diagnostic for DM, but samples are only taken during post-mortem examination (Awano et al. 2009; Coates & Wininger 2010; Johnston et al. 2000; Miller et al. 2009). A tentative ante-mortem diagnosis may be made on characteristic clinical presentation in the absence of other thoracolumbar myelopathy aetiologies (Awano et al. 2009; Coates et al. 2007; Coates & Wininger 2010).
Other disease processes may coexist or even mimic and confound a definitive diagnosis of DM, including degenerative lumbosacral syndrome, intervertebral disc disease, spinal cord neoplasia and degenerative joint diseases such as hip dysplasia or cranial cruciate ligament rupture (Coates & Wininger 2010). The historical finding of cranial cruciate ligament injury of the affected Boxer dog (3 years old) in the present study could indicate that there may be a link between these coexisting disease processes and DM. An affected genotyped dog will greatly increase the suspicion of DM as being the definitive diagnosis only in patients presenting with the characteristic clinical signs. Other ante-mortal diagnostic tests have included magnetic resonance imaging (Coates & Wininger 2010), computer tomography (Jones et al. 2005), cerebrospinal fluid examination (Kamishina et al. 2008; Oji et al. 2007), electrodiagnostic testing (Coates et al. 2007; Shelton et al. 2012) and neuromuscular biopsies (Awano et al. 2009; Coates & Wininger 2010; Shelton et al. 2012), which may assist in definitively diagnosing DM; however, these diagnostic tests are not always positive (Awano et al. 2009; Coates & Wininger 2010; Okada et al. 2009; Oliver 1993). A definitive diagnosis of DM in the ante-mortal stage remains a challenge (Coates & Wininger 2010). The link between the genotypic expression of the SOD1 mutation, the histopathological findings and the clinical manifestation cannot be ignored.
Previous studies have indicated that both normal and carrier dogs present with clinical signs of DM; however, these findings were not definitively diagnosed on histopathology and thus other possible aetiological causes cannot be excluded (Awano et al. 2009; Coates & Wininger 2010). Carrier dogs do have characteristic immuno-histopathological lesions that react with antibodies against the faulty SOD1 protein as in affected dogs, but are not associated with clinical manifestation of the disease (Awano et al. 2009; Barclay & Haines 1994; Coates & Wininger 2010), perhaps due to incomplete penetrance.
Degenerative myelopathy was not definitively diagnosed in any of the participating Boxer dogs in the present study and thus disease prevalence could not be calculated or estimated. The calculated point prevalence and overall prevalence were therefore based on detecting affected genotyped Boxer dogs in the FBCSA population. The overall prevalence of affected genotyped Boxer dogs was determined to be 0.23%, which is close to the current overall estimated prevalence of diagnosed DM of 0.19% (Coates et al. 2007; Shelton et al. 2012). These results indicate that DM should not be ignored as a possible differential diagnosis in aged Boxer dogs presenting with pelvic limb abnormalities. The clinical significance of this finding is difficult to appreciate at present as the affected dog did have a history of pelvic limb pathology characteristic of cranial cruciate ligament injury and not of DM. Due to the old age onset and progressive nature of the disease, the genotyping may become clinically significant in the future.
The present study concludes that genotyping of the missense mutation in Boxer dogs is possible in South Africa and that there are carrier and affected Boxer dogs in the South African population. This makes degenerative myelopathy a plausible diagnosis in aged dogs presenting with pelvic limb pathology. Owing to the late onset and insidious nature of the disease process, owners of Boxer dogs (and other commonly affected breeds) should consider genotyping prior to breeding.
The authors would like to thank the FBCSA and owners of the Boxer dogs for participating in this study. Publication of this article was sponsored by the Wildlife Group (http://www.vets4wildlife.co.za) of the South African Veterinary Association.
The authors declare that they have no financial or personal relationship(s) that may have inappropriately influenced them in writing this article.
M.C.O. (University of Pretoria) liaison between the Federation of Boxer Clubs of Southern Africa and other investigators, and organiser of sample collection days. H.v.d.Z. (Inqaba Biotec) genetic testing of Boxer dogs samples. G.E.Z. (University of Pretoria) collection of samples from Boxer dogs and publication writing.
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Private Bag X04
Onderstepoort 0110, South Africa
Received: 18 Feb. 2013
Accepted: 10 May 2013
Published: 27 Sept. 2013