Using genetic markers to select Canadian Duroc sires for lower boar taint levels in commercial hogs

Mohsen Jafarikia1,2, Laurence Maignel1, Frédéric Fortin3, Stefanie Wyss1, Wim Van Berkel4, Dan Cohoe5, Flavio Schenkel2, Jim Squires2, Brian Sullivan1

1Canadian Centre for Swine Improvement Inc., #75-960 Carling Ave., Central Experimental Farm, Ottawa, Ontario, Canada, K1A 0C6
2Department of Animal & Poultry Science, University of Guelph, 50 Stone Road East, Guelph, Ontario, Canada, N1G 2W1
3Centre de développement du porc du Québec, Place de la Cité, tour Belle Cour 450-2590, boulevard Laurier, Québec City, Québec,Canada, G1V 4M6
4Western Swine Association Testing, Lacombe, Alberta
5Ontario Swine Improvement, Box 400, Innerkip, Ontario, Canada, N0J 1M0

Abstract: The feasibility of genetic selection against boar taint in sire lines to reduce levels of taint in commercial progeny was investigated. Androstenone is the main compound responsible for boar taint and in a previous study, about 50% of Duroc boars exceeded the consumer acceptance level. A total of 1,079 Duroc boars were genotyped for 97 SNP markers in candidate genes known to be involved in metabolism of androstenone and skatole, from which 60 markers had a MAF>0.05. The natural logarithm of androstenone levels in fat samples of 580 boars, weighing between 90 kg and 150 kg and less than 300 days old, were used to estimate the effects of SNPs. A two-step analysis was performed. First, the SAS GLM procedure was used to adjust phenotypes for season and the boar�s age and weight at time of sampling. In a second step, residuals of the GLM procedure were used in a backward elimination in the SAS REG procedure to identify the best fitting model. The estimated effects of 17 significant SNPs were used to calculate marker-assisted estimated breeding values (MEBVs) for androstenone levels for 452 AI boars. The top and bottom 30 boars with extreme MEBVs were selected to produce commercial Duroc X Landrace/Yorkshire progeny. Average androstenone MEBVs in high and low sire groups were 1.82 and 0.94, respectively. Assuming additive effects for selected SNPs and random sampling of dams, it is expected that the difference between average levels of androstenone in commercial progeny of high and low sire groups would be 0.44 in log scale. Therefore, MEBVs for androstenone seem promising and will be validated in commercial trials.

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Presented at the 66th EAAP Annual General Meeting, August 31-September 4, 2015, Warsaw, Poland