Peer-reviewed veterinary case report
Gene linked to uterine infection pyometra in golden retriever dogs
By Arendt, Maja et al.·Published in Scientific reports·2021·Faculty of Health and Medical Sciences·View original on PubMed →
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Original publication title: The ABCC4 gene is associated with pyometra in golden retriever dogs.
- Species:
- dog
Plain-English summary
A study found that female golden retrievers are at a higher risk for developing pyometra, a serious infection of the uterus, due to genetic factors. Pyometra can cause symptoms like fever, lethargy, and a discharge from the vulva. Researchers identified a specific gene, ABCC4, that may be linked to this condition in golden retrievers. This gene plays a role in transporting important substances in the body. Understanding this genetic link could help in identifying dogs at risk and developing preventive measures.
People also search for: golden retriever pyometra symptoms · female dog uterine infection treatment · genetic risk factors pyometra in dogs
Abstract
Pyometra is one of the most common diseases in female dogs, presenting as purulent inflammation and bacterial infection of the uterus. On average 20% of intact female dogs are affected before 10 years of age, a proportion that varies greatly between breeds (3-66%). The clear breed predisposition suggests that genetic risk factors are involved in disease development. To identify genetic risk factors associated with the disease, we performed a genome-wide association study (GWAS) in golden retrievers, a breed with increased risk of developing pyometra (risk ratio: 3.3). We applied a mixed model approach comparing 98 cases, and 96 healthy controls and identified an associated locus on chromosome 22 (p = 1.2 × 10, passing Bonferroni corrected significance). This locus contained five significantly associated SNPs positioned within introns of the ATP-binding cassette transporter 4 (ABCC4) gene. This gene encodes a transmembrane transporter that is important for prostaglandin transport. Next generation sequencing and genotyping of cases and controls subsequently identified four missense SNPs within the ABCC4 gene. One missense SNP at chr22:45,893,198 (p.Met787Val) showed complete linkage disequilibrium with the associated GWAS SNPs suggesting a potential role in disease development. Another locus on chromosome 18 overlapping the TESMIN gene, is also potentially implicated in the development of the disease.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/34404837/