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J. Dairy Sci. 89:4874-4885
© American Dairy Science Association, 2006.

Multiple-Trait Multiple-Country Genetic Evaluations for Udder Health Traits

T. Mark*,{dagger},1 and P. G. Sullivan{ddagger},§

* Interbull Centre, Department of Animal Breeding and Genetics, Swedish University of Agricultural Sciences, Box 7023, 750 07 Uppsala, Sweden
{dagger} Department of Large Animal Sciences, The Royal Veterinarian and Agricultural University, Grønnegårdsvej 8, 1870 Frederiksberg C, Denmark
{ddagger} Beef Improvement Ontario, 660 Speedvale Ave. W., Suite 102, Guelph, Ontario N1K 1E5, Canada
§ Canadian Dairy Network, 150 Research Lane, Guelph, Ontario N1G 4T2, Canada

1 Corresponding author: thm{at}kvl.dk

International genetic bull evaluations of somatic cell counts (SCC) from 8 different Holstein populations and clinical mastitis from 3 of these populations were inferred simultaneously using a multiple-trait–multiple-country evaluation (MT-MACE) model. This model considered effective independent weighting factors and multivariately deregressed national genetic evaluations for countries with multiple-trait national models. Predictions of genetic merit from MT-MACE and their reliabilities were compared with the corresponding results from 2 separate single-trait–multiple-country evaluations (ST-MACE) for different groups of bulls. The assumed heritabilities for clinical mastitis (h2 = 0.02 to 0.05) were substantially lower than the heritabilities for SCC (h2 = 0.08 to 0.27). The predictive ability of MT-MACE was essentially equal to or better than the predictive ability of ST-MACE for all country-trait combinations, but both methods yielded effectively unbiased and consistent consecutive predictions (correlation > 0.93). Both sets of predictions also agreed well with future national genetic evaluations for bulls receiving additional daughter information (correlation > 0.96), except for evaluations for which within-country correlations were utilized internationally, but not nationally (correlation = 0.86 to 0.97). The reliabilities for MT-MACE were essentially equal to or higher than reliabilities for ST-MACE, depending on the trait and group of bulls in question. Reliabilities increased most for young bulls, and for clinical mastitis in countries that did not use the within-country correlations with SCC in the national evaluation (up to a 23% increase in average reliability).

Key Words: multiple trait • international genetic evaluation • clinical mastitis • somatic cell concentration




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