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Peer-reviewed veterinary case report

Stable genetic variant linked to Shar-Pei dog fever disease

By Olsson, M et al.·Published in BMC genomics·2016·Department of Medicine·View original on PubMed

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Original publication title: Absolute quantification reveals the stable transmission of a high copy number variant linked to autoinflammatory disease.

Species:
dog

Plain-English summary

A group of Shar-Pei dogs with recurrent fever was studied to understand a genetic variant linked to a complex autoinflammatory disease. Researchers used a new testing method called droplet digital PCR (ddPCR) to measure specific genetic changes more accurately. They found that a particular variant (CNV_16.1) significantly increased the risk of developing this disease. The results suggest that this genetic test could help breeders reduce the number of affected dogs by identifying those carrying the harmful variant.

People also search for: Shar-Pei recurrent fever treatment · autoinflammatory disease in dogs · genetic testing for Shar-Pei dogs

Abstract

BACKGROUND: Dissecting the role copy number variants (CNVs) play in disease pathogenesis is directly reliant on accurate methods for quantification. The Shar-Pei dog breed is predisposed to a complex autoinflammatory disease with numerous clinical manifestations. One such sign, recurrent fever, was previously shown to be significantly associated with a novel, but unstable CNV (CNV_16.1). Droplet digital PCR (ddPCR) offers a new mechanism for CNV detection via absolute quantification with the promise of added precision and reliability. The aim of this study was to evaluate ddPCR in relation to quantitative PCR (qPCR) and to assess the suitability of the favoured method as a genetic test for Shar-Pei Autoinflammatory Disease (SPAID). RESULTS: One hundred and ninety-six individuals were assayed using both PCR methods at two CNV positions (CNV_14.3 and CNV_16.1). The digital method revealed a striking result. The CNVs did not follow a continuum of alleles as previously reported, rather the alleles were stable and pedigree analysis showed they adhered to Mendelian segregation. Subsequent analysis of ddPCR case/control data confirmed that both CNVs remained significantly associated with the subphenotype of fever, but also to the encompassing SPAID complex (p < 0.001). In addition, harbouring CNV_16.1 allele five (CNV_16.1|5) resulted in a four-fold increase in the odds for SPAID (p < 0.001). The inclusion of a genetic marker for CNV_16.1 in a genome-wide association test revealed that this variant explained 9.7 % of genetic variance and 25.8 % of the additive genetic heritability of this autoinflammatory disease. CONCLUSIONS: This data shows the utility of the ddPCR method to resolve cryptic copy number inheritance patterns and so open avenues of genetic testing. In its current form, the ddPCR test presented here could be used in canine breeding to reduce the number of homozygote CNV_16.1|5 individuals and thereby to reduce the prevalence of disease in this breed.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/27107962/