Journal article
The Association between the Abundance of Homozygous Deleterious Variants and the Morbidity of Dog Breeds
Biology , Vol.13(8), pp.1-8
2024
PMCID: PMC11351664
PMID: 39194512
Abstract
It is well known that highly inbred dogs are more prone to diseases than less inbred or outbred dogs. This is because inbreeding increases the load of recessive deleterious variants. Using the genomes of 392 dogs belonging to 83 breeds, we investigated the association between the abundance of homozygous deleterious variants and dog health. We used the number of non-routine veterinary care events for each breed to assess the level of morbidity. Our results revealed a highly significant positive relationship between the number of homozygous deleterious variants located within the runs of homozygosity (RoH) tracts of the breeds and the level of morbidity. The dog breeds with low morbidity had a mean of 87 deleterious SNVs within the RoH, but those with very high morbidity had 187 SNVs. A highly significant correlation was also observed for the loss-of-function (LoF) SNVs within RoH tracts. The dog breeds that required more veterinary care had 2.3 times more homozygous LoF SNVs than those that required less veterinary care (112 vs. 50). The results of this study could be useful for understanding the disease burden on breed dogs and as a guide for dog breeding programs.
Details
- Title
- The Association between the Abundance of Homozygous Deleterious Variants and the Morbidity of Dog Breeds
- Authors
- Sankar Subramanian (Corresponding Author) - University of the Sunshine Coast, Queensland, Centre for BioinnovationManoharan Kumar - James Cook University
- Publication details
- Biology , Vol.13(8), pp.1-8
- Publisher
- MDPI AG
- Date published
- 2024
- DOI
- 10.3390/biology13080574
- ISSN
- 2079-7737
- PMID
- 39194512; PMC11351664
- Copyright note
- © 2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
- Data Availability
- This present study did not generate any new data and only used the genome data available from public repositories and previous studies.
- Grant note
- This study was supported by a grant from the University of the Sunshine Coast to S.S.
- Organisation Unit
- School of Science, Technology and Engineering; Centre for Bioinnovation
- Language
- English
- Record Identifier
- 991055298102621
- Output Type
- Journal article
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