Hostname: page-component-cd9895bd7-8ctnn Total loading time: 0 Render date: 2024-12-26T13:27:58.174Z Has data issue: false hasContentIssue false

Genetic parameters for endocrine and traditional fertility traits, hyperketonemia and milk yield in dairy cattle

Published online by Cambridge University Press:  29 June 2018

J. Häggman*
Affiliation:
Department of Agricultural Sciences, University of Helsinki, FI-00014 Helsinki, Finland
J. M. Christensen
Affiliation:
Lattec I/S, Slangerupgade 69, 3400 Hillerod, Denmark
E. A. Mäntysaari
Affiliation:
Natural Resources Institute Finland (Luke), Green Technology, FI-31600 Jokioinen, Finland
J. Juga
Affiliation:
Department of Agricultural Sciences, University of Helsinki, FI-00014 Helsinki, Finland
*
Get access

Abstract

High-yielding cows may suffer from negative energy balance during early lactation, which can lead to ketosis and delayed ability of returning to cyclicity after calving. Fast recovery after calving is essential when breeding for improved fertility. Traditionally used fertility traits, such as the interval from calving to first insemination (CFI), have low heritabilities and are highly influenced by management decisions. Herd Navigator™ management program samples and analyses milk progesterone and β-hydroxybutyrate (BHB) automatically during milking. In this study, the genetic parameters of endocrine fertility traits (measured from milk progesterone) and hyperketonemia (measured from milk BHB) in early lactation were evaluated and compared with traditional fertility traits (CFI, interval from calving to the last insemination and interval from first to last insemination) and the milk yield in red dairy cattle herds in Finland. Data included observations from 14 farms from 2014 to 2017. Data were analyzed with linear animal models using DMU software and analyses were done for first parity cows. Heritability estimates for traditional fertility traits were low and varied between 0.03 and 0.07. Estimated heritabilities for endocrine fertility traits (interval from calving to the first heat (CFH) and commencement of luteal activity (C-LA)) were higher than for traditional fertility traits (0.19 to 0.33). Five slightly different hyperketonemia traits divided into two or three classes were studied. Linear model heritability estimates for hyperketonemia traits were low, however, when the threshold model was used for binary traits the estimates became slightly higher (0.07 to 0.15). Genetic correlation between CFH and C-LA for first parity cows was high (0.97) as expected since traits are quite similar. Moderate genetic correlations (0.47 to 0.52) were found between the endocrine fertility traits and early lactation milk yield. Results suggest that the data on endocrine fertility traits measured by automatic systems is a promising tool for improving fertility, specifically when more data is available. For hyperketonemia traits, dividing values into three classes instead of two seemed to work better. Based on the current study and previous studies, where higher heritabilities have been found for milk BHB traits than for clinical ketosis, milk BHB traits are a promising indicator trait for resistance to ketosis and should be studied more. It is important that this kind of data from automatic devices is made available to recording and breeding organizations in the future.

Type
Research Article
Copyright
© The Animal Consortium 2018 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Berry, DP, Wall, E and Pryce, JE 2014. Genetics and genomics of reproductive performance in dairy and beef cattle. Animal 8 (suppl. 1), 115121.Google Scholar
Blom, JY, Christensen, JM and Ridder, C 2015. Real-time analyses of BHB in milk can monitor ketosis and its impact on reproduction in dairy cows. In Precision livestock farming applications (ed. I Halachmi), pp. 263272. Wageningen Academic Publishers, Wageningen, The Netherlands.Google Scholar
Bulman, DC and Lamming, G 1978. Milk progesterone levels in relation to conception, repeat breeding and factors influencing a cyclicity in dairy cows. Journal of Reproduction Fertility 54, 447458.Google Scholar
Dempster, E and Lerner, I 1950. Heritability of threshold characters. Genetics 35, 212236.Google Scholar
Denis-Robichaud, J, Dubuc, J, Lefebvre, D and DesCôteaux, L 2014. Accuracy of milk ketone bodies from flow-injection analysis for the diagnosis of hyperketonemia in dairy cows. Journal of Dairy Science 97, 33643370.Google Scholar
Duffield, TF, Lissemore, KD, McBride, BW and Leslie, K 2009. Impact of hyperketonemia in early lactation dairy cows on health and production. Journal of Dairy Science 92, 571580.Google Scholar
Faba 2017. Terveystarkkailun tulokset 2016. Retrieved on 8 December 2017 from http://www.faba.fi/fi/tietopankki/terveystarkkailu.Google Scholar
Friggens, NC, Bjerring, M, Ridder, C, Højsgaard, S and Larsen, T 2008. Improved detection of reproductive status in dairy cows using milk progesterone measurements. Reproduction in Domestic Animals 43, 113121.Google Scholar
Hoekstra, J, van der Lugt, AW, van der Werf, JHJ and Ouweltjes, W 1994. Genetic and phenotypic parameters for milk production and fertility traits in upgraded dairy cattle. Livestock Production Science 40, 225232.Google Scholar
Ismael, A, Strandberg, E, Kargo, M, Fogh, A and Løvendahl, P 2015. Estrus traits derived from activity measurements are heritable and closely related to the time from calving to first insemination. Journal of Dairy Science 98, 34703477.Google Scholar
Koeck, A, Jamrozik, J, Kistemaker, G, Schenkel, F, Moore, R, Lefebvre, D, Kelton, D and Miglior, F 2016. Genetic and phenotypic associations of milk β-hydroxybutyrate with ketosis in Canadian Holsteins. Canadian Journal of Animal Science 96, 302305.Google Scholar
Koeck, A, Jamrozik, J, Schenkel, FS, Moore, RK, Lefebvre, DM, Kelton, DF and Miglior, F 2014. Genetic analysis of milk β-hydroxybutyrate and its association with fat-to-protein ratio, body condition score, clinical ketosis, and displaced abomasum in early first lactation of Canadian Holsteins. Journal of Dairy Science 97, 72867292.Google Scholar
LeBlanc, S 2010. Monitoring metabolic health of dairy cattle in the transition period. Journal of Reproduction and Development 56, 2935.Google Scholar
Lee, S, Cho, K, Park, M, Choi, T, Kim, S and Do, C 2016. Genetic parameters of milk β-hydroxybutyric acid and acetone and their genetic association with milk production traits of holstein cattle. Asian-Australasian Journal of Animal Sciences 29, 15301540.Google Scholar
Løvendahl, P and Chagunda, MGG 2009. Genetic variation in estrus activity traits. Journal of Dairy Science 92, 46834688.Google Scholar
Madsen, P and Jensen, J 2013. A user’s guide to DMU. A package for analysing multivariate mixed models. Version 6, release 5.2. Department of Genetics and Biotechnology, Faculty of Life Sciences, University of Aarhus, Research Centre Foulum, Tjele, Denmark.Google Scholar
Miglior, F, Koeck, A, Jamrozik, J, Schenkel, FS, Kelton, DF, Kistemaker, GJ and Van Doormaal, BJ 2014. Index for mastitis resistance and use of BHBA for evaluation of health traits in Canadian Holsteins. Interbull Bulletin 48, 7378.Google Scholar
Muuttoranta, K, Tyrisevä, A-M, Mäntysaari, EA, Pösö, J, Aamand, GP, Eriksson, J-Å, Nielsen, US and Lidauer, MH 2015. Genetic parameters for female fertility in Nordic dairy cattle. Interbull Bulletin 49, 3235.Google Scholar
NAV 2018. NTM – Nordic total merit. Retrieved on 9 March 2018 from http://www.nordicebv.info.Google Scholar
Nielsen, NI, Friggens, NC, Chagunda, MGG and Ingvartsen, KL 2005. Predicting risk of ketosis in dairy cows using in-line measurements of β-Hydroxybutyrate: a biological model. Journal of Dairy Science 88, 24412453.Google Scholar
Nielsen, NI, Hameleers, A, Young, FJ, Larsen, T and Friggens, NC 2010. Energy intake in late gestation affects blood metabolites in early lactation independently of milk production in dairy cows. Animal 4, 5260.Google Scholar
Nyman, S, Johansson, K, de Koning, DJ, Berry, DP, Veerkamp, RF, Wall, E and Berglund, B 2014. Genetic analysis of atypical progesterone profiles in Holstein-Friesian cows from experimental research herds. Journal of Dairy Science 97, 72307239.Google Scholar
Oetzel, GR 2007. Herd-level ketosis–diagnosis and risk factors. In Proceedings of the 40th Annual Conference of American Association of Bovine Practitioners, 20–22 September 2007, Vancouver, Canada, pp. 67–91.Google Scholar
Petersson, KJ, Berglund, B, Strandberg, E, Gustafsson, H, Flint, APF, Woolliams, JA and Royal, MD 2007. Genetic analysis of postpartum measures of luteal activity in dairy cows. Journal of Dairy Science 90, 427434.Google Scholar
Pollott, GE and Coffey, M 2008. The effect of genetic merit and production system on dairy cow fertility, measured using progesterone profiles and on-farm recording. Journal of Dairy Science 91, 36493660.Google Scholar
Pryce, JE, Gaddis, KP, Koeck, A, Bastin, C, Abdelsayed, M, Gengler, N, Miglior, F, Heringstad, B, Egger-Danner, C and Stock, K 2016. Invited review: opportunities for genetic improvement of metabolic diseases. Journal of Dairy Science 99, 68556873.Google Scholar
Rajala-Schultz, PJ, Grohn, YT and McCulloch, CE 1999. Effects of milk fever, ketosis, and lameness on milk yield in dairy cows. Journal of Dairy Science 82, 288294.Google Scholar
Royal, MD, Flint, APF and Woolliams, JA 2002. Genetic and phenotypic relationships among endocrine and traditional fertility traits and production traits in Holstein-Friesian dairy cows. Journal of Dairy Science 85, 958967.Google Scholar
Samsonova, JV, Safronova, VA and Osipov, AP 2015. Pretreatment-free lateral flow enzyme immunoassay for progesterone detection in whole cows’ milk. Talanta 132, 685689.Google Scholar
Tenghe, AMM, Bouwman, AC, Berglund, B, Strandberg, E, Blom, JY and Veerkamp, RF 2015. Estimating genetic parameters for fertility in dairy cows from in-line milk progesterone profiles. Journal of Dairy Science 98, 57635773.Google Scholar
van der Drift, SGA, van Hulzen, KJE, Teweldemedhn, TG, Jorritsma, R, Nielen, M and Heuven, HCM 2012. Genetic and nongenetic variation in plasma and milk β-hydroxybutyrate and milk acetone concentrations of early-lactation dairy cows. Journal of Dairy Science 98, 67816787.Google Scholar
Veerkamp, R, Beerda, B and van der Lende, T 2003. Effects of genetic selection for milk yield on energy balance, levels of hormones, and metabolites in lactating cattle, and possible links to reduced fertility. Livestock Production Science 83, 257275.Google Scholar