Between- and within-herd variation in blood and milk biomarkers in Holstein cows in early lactation

被引:18
|
作者
Krogh, M. A. [1 ]
Hostens, M. [2 ]
Salavati, M. [3 ,11 ]
Grelet, C. [4 ]
Sorensen, M. T. [1 ]
Wathes, D. C. [3 ]
Ferris, C. P. [5 ]
Marchitelli, C. [6 ]
Signorelli, F. [6 ]
Napolitano, F. [6 ]
Becker, F. [7 ]
Larsen, T. [1 ]
Matthews, E. [8 ]
Carter, F. [8 ]
Vanlierde, A. [4 ]
Opsomer, G. [2 ]
Gengler, N. [9 ]
Dehareng, F. [4 ]
Crowe, M. A. [8 ]
Ingvartsen, K. L. [1 ]
Foldager, L. [1 ,10 ]
机构
[1] Aarhus Univ, Dept Anim Sci, Blichers Alle 20, DK-8830 Tjele, Denmark
[2] Univ Ghent, Dept Reprod Obstet & Herd Hlth, Salisburylaan 133, B-9820 Merelbeke, Belgium
[3] Royal Vet Coll, Dept Pathobiol & Populat Sci, Hawkshead Lane, Hatfield AL9 7TA, Herts, England
[4] Walloon Agr Res Ctr, Valorizat Agr Prod Dept, B-5030 Gembloux, Belgium
[5] Agrifood & Biosci Inst, Largepk, Hillsborough BT26 6DR, North Ireland
[6] Res Ctr Anim Prod & Aquaculture, Via Salaria 31, I-00015 Monterotondo, Italy
[7] Leibniz Inst Farm Anim Biol, Inst Reprod Biol, Wilhelm Stahl Allee 2, D-18196 Dummerstorf, Germany
[8] Univ Coll Dublin, Vet Sci Ctr Belfield, Sch Vet Med, Dublin 4, Ireland
[9] Univ Liege, Gembloux Agrobio Tech, Passage Deportes 2, B-5030 Gembloux, Belgium
[10] Aarhus Univ, Bioinformat Res Ctr, CF Mollers Alle 8, DK-8000 Aarhus, Denmark
[11] Roslin Inst, Genet & Genom Div, Easter Bush Campus, Roslin EH25 9RG, Midlothian, Scotland
关键词
dairy; biomarker; physiological imbalance; variance; monitoring; DAIRY-COWS; FLUOROMETRIC-DETERMINATION; BETA-HYDROXYBUTYRATE; DIURNAL-VARIATION; SAMPLING TIME; FREE GLUCOSE; GLUCOSE-6-PHOSPHATE; INDICATORS; NUTRITION; PLASMA;
D O I
10.1017/S1751731119002659
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
Both blood- and milk-based biomarkers have been analysed for decades in research settings, although often only in one herd, and without focus on the variation in the biomarkers that are specifically related to herd or diet. Biomarkers can be used to detect physiological imbalance and disease risk and may have a role in precision livestock farming (PLF). For use in PLF, it is important to quantify normal variation in specific biomarkers and the source of this variation. The objective of this study was to estimate the between- and within-herd variation in a number of blood metabolites (beta-hydroxybutyrate (BHB), non-esterified fatty acids, glucose and serum IGF-1), milk metabolites (free glucose, glucose-6-phosphate, urea, isocitrate, BHB and uric acid), milk enzymes (lactate dehydrogenase and N-acetyl-beta-D-glucosaminidase (NAGase)) and composite indicators for metabolic imbalances (Physiological Imbalance-index and energy balance), to help facilitate their adoption within PLF. Blood and milk were sampled from 234 Holstein dairy cows from 6 experimental herds, each in a different European country, and offered a total of 10 different diets. Blood was sampled on 2 occasions at approximately 14 days-in-milk (DIM) and 35 DIM. Milk samples were collected twice weekly (in total 2750 samples) from DIM 1 to 50. Multilevel random regression models were used to estimate the variance components and to calculate the intraclass correlations (ICCs). The ICCs for the milk metabolites, when adjusted for parity and DIM at sampling, demonstrated that between 12% (glucose-6-phosphate) and 46% (urea) of the variation in the metabolites' levels could be associated with the herd-diet combination. Intraclass Correlations related to the herd-diet combination were generally higher for blood metabolites, from 17% (cholesterol) to approximately 46% (BHB and urea). The high ICCs for urea suggest that this biomarker can be used for monitoring on herd level. The low variance within cow for NAGase indicates that few samples would be needed to describe the status and potentially a general reference value could be used. The low ICC for most of the biomarkers and larger within cow variation emphasises that multiple samples would be needed - most likely on the individual cows - for making the biomarkers useful for monitoring. The majority of biomarkers were influenced by parity and DIM which indicate that these should be accounted for if the biomarker should be used for monitoring.
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收藏
页码:1067 / 1075
页数:9
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