Index for Mastitis Resistance and Use of BHBA for Evaluation of Health Traits in Canadian Holsteins

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Index for Mastitis Resistance and Use of BHBA for Evaluation of Health Traits in Canadian Holsteins Filippo Miglior 1,2, Astrid Koeck 2, Janusz Jamrozik 1, Flavio Schenkel 2, David Kelton 3, Gerrit Kistemaker 1, and Brian Van Doormaal 1 1 Canadian Dairy Network, 2 CGIL, University of Guelph, 3 Ontario Veterinary College, University of Guelph

Genetic evaluation for mastitis resistance In August 2014, first official run of genetic evaluations for mastitis resistance Multiple-trait linear animal model (Jamrozik et al., 2013) First vs. later parities: clinical mastitis, mean SCS, standard deviation of SCS, excessive test-day SCC First parity cows: udder depth, fore udder attachment, body condition score Genetic evaluations expressed as relative breeding values (RBV) with a mean of 100 and a SD of 5 (higher values are desirable)

Objective Development of a Mastitis Resistance Index Clinical mastitis in first lactation (CM-F) Clinical mastitis in later lactations (CM-L) SCS from Canadian Test Day Model

Why an index? Why not using just mastitis EBV? Mastitis EBV are indicators of clinical mastitis SCS EBV are indicators of subclinical mastitis 4 3,5 SCS EBV 3 2,5 2 80 85 90 95 100 105 110 115 120 Clinical Mastitis EBV 4

Boettcher et al., 1998 Udder health index Subclinical mastitis (measured by SCS) in lactations 1 and 2 Clinical mastitis in lactations 1 and 2 Milking time Estimated economic weights were -$12, -$31, -$15, -$59 and -$11, respectively, per genetic standard deviation. At that time clinical mastitis was not recorded, thus traits in the selection index were milking speed, udder conformation and SCS in first and later lactations

Mastitis Resistance Index Based on the work by Boettcher et al. (1998) Mastitis Resistance (MR) = 1/3 CM-F + 1/3 CM-L - 1/3 SCS where; CM-F = Clinical Mastitis in First lactation CM-L = Clinical Mastitis in Later lactations SCS = overall SCS evaluation as officially published whereby low values are desired

Selection response Assumptions Heritability for CM-F, CM-L and SCS = 0.03, 0.05, 0.20, respectively Genetic correlations among the three traits: CM-F with CM-L = 0.60 and 0.55 for the other 2 combinations Reliability of RBV for MR traits = 0.30, and for SCS = 0.50 (conservative estimates) Selection only on Mastitis Resistance (with various combinations/emphasis among 3 traits) 7

Selection response Weights Genetic gain per year (RBV points) CM-F CM-L SCS CM-F CM-L SCS 1/3 1/3 1/3 0.14 0.19 0.44 0.5 0.5 0 0.13 0.18 0.24 0 0 1 0.13 0.17 0.63 1 0 0 0.15 0.12 0.21 0 1 0 0.11 0.23 0.25 1/6 3/6 2/6 0.13 0.20 0.44 0.5 0 0.5 0.15 0.16 0.50

Genetic trends Sire RBV CM-F CM-L SCS 105 104 103 102 101 100 99 98 97 96 95 1997 1999 2001 2003 2005 2007 Year of birth 9

Conclusions New index for Mastitis Resistance Equal weights for CM-F, CM-L and SCS 2/3 on clinical mastitis and 1/3 on SCS Equal weight between clinical mastitis in first vs. later Expressed on RBV scale, mean of 100, SD of 5 Higher value is desirable At least 45 REL with 10 daughters in 10 herds Higher accuracy of selection for both clinical and subclinical mastitis 10

Use of BHBA for Evaluation of Health Traits in Canadian Holsteins

Milk ß-hydroxybutyrate (BHBA) Hyperketonemia or ketosis is one of the most frequent diseases in dairy cattle Level of milk ß-hydroxybutyrate (BHBA) is an indicator of subclinical ketosis Since October 2011 screening for hyperketonemia based on a BHBA analysis by MIR of test-day milk samples is offered in Canada by Valacta

Objective Estimate genetic parameters for milk BHBA in first lactation Holstein cows Determine genetic correlations between milk BHBA and metabolic diseases (clinical ketosis and displaced abomasum)

Mean milk BHBA Mean milk BHBA mmol/l 0,16 0,14 0,12 0,1 0,08 0,06 0,04 5 15 25 35 45 55 65 75 85 95 Days in milk

Proportion (%) of cows with a positive (milk BHBA 0.20 mmol/l) test result % of first lactation cows 20 18 16 14 12 10 8 6 4 2 0 5 15 25 35 45 55 65 75 85 95 Days in milk

Analysis of milk BHBA Trait DIM Records, no. Mean BHBA 1, mmol/l 5-20 20,845 0.115 BHBA 2, mmol/l 21-40 26,871 0.094 BHBA 3, mmol/l 41-60 27,404 0.075 BHBA 4, mmol/l 61-80 27,233 0.068 BHBA 5, mmol/l 81-100 26,811 0.067 16

Heritabilities and genetic correlations Trait BHBA 1 BHBA 2 BHBA 3 BHBA 4 BHBA 5 BHBA 1 0.13 0.96 0.84 0.75 0.67 BHBA 2 0.13 0.99 0.85 0.77 BHBA 3 0.16 0.98 0.96 BHBA 4 0.22 0.99 BHBA 5 0.29

Associations between milk BHBA and metabolic diseases Milk BHBA at the first test-day (5-40 DIM) Ketosis Displaced abomasum Trait Records, no. Mean BHBA, mmol/l 7,635 0.10 KET frequency, % 3,437 3.61 DA frequency, % 6,894 2.74 18

Frequency of clinical ketosis and displaced of negative, suspect and positive tested cows Disease frequency (%) 12 10 8 6 4 2 0 Negative Suspect Positive Clinical ketosis Displaced abomasum 19

Heritabilities and genetic correlations Trait BHBA KET DA BHBA 0.13 (0.01) 0.50 (0.26) 0.21 (0.16) KET 0.03 (0.03) 0.63 (0.43) DA 0.05 (0.02) 20

Conclusions Heritabilities for milk BHBA ranging from 0.13 to 0.29 Higher milk BHBA in early lactation was genetically associated with a higher frequency of clinical ketosis and displaced abomasum Milk BHBA can be routinely analyzed in milk samples on test-days, and, therefore, provide a practical tool for breeding cows with a lower susceptibility to hyperketonemia 21

Summer 2014