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Oral supplementation of medium-chain fatty acids during the dry period supports the neutrophil viability of peripartum dairy cows

Published online by Cambridge University Press:  10 April 2013

Sofie Piepers*
Affiliation:
M-team and Mastitis and Milk Quality Research Unit, Department of Reproduction, Obstetrics, and Herd Health, Faculty of Veterinary Medicine, Ghent University, Merelbeke, Belgium
Sarne De Vliegher
Affiliation:
M-team and Mastitis and Milk Quality Research Unit, Department of Reproduction, Obstetrics, and Herd Health, Faculty of Veterinary Medicine, Ghent University, Merelbeke, Belgium
*
*For correspondence; e-mail: [email protected]

Abstract

A randomised clinical trial was conducted to explore the effect of orally supplemented medium-chain fatty acids (MCFA) to heifers and cows starting 6–8 weeks prior to expected calving date on blood and milk polymorphonuclear neutrophilic leucocyte (PMNL) apoptosis between 1 and 3 d in milk (DIM). The effects of MCFA-supplementation on the likelihood of intramammary infections (IMI) in early lactation, and test-day somatic cell count (SCC) and average daily milk yield (MY) during the first 4 months of lactation were evaluated as well. Twenty-two animals were included of which half were orally supplemented with MCFA starting 6–8 weeks prior to calving and half served as non-supplemented controls. The PMNL viability in both blood and milk was quantified using dual-colour flow cytometry with fluorescein-labelled annexin and propidium iodide. In non-supplemented animals, % blood PMNL apoptosis significantly increased between start of supplementation and early lactation, reflecting a potential reduction in innate immune capacity, whereas this was not true in the MCFA-supplemented animals. Similar results were seen in milk PMNL apoptosis. Overall, the % apoptotic milk PMNL between 1 and 3 DIM was significantly lower in the MCFA-supplemented group compared with the non-supplemented group. There was no substantial effect of oral MCFA-supplementation on the likelihood of quarter IMI nor on the composite test-day milk SCC or average daily MY. In conclusion, oral MCFA-supplementation starting 6–8 weeks before expected calving date supported the blood and milk neutrophil viability in early lactating dairy cows. Still, this was not reflected in an improvement of udder health nor MY in early and later lactation. The results should trigger research to further unravel the mechanisms behind the observed immunomodulating effect, and the potential relevance for the cows' performances throughout lactation.

Type
Research Article
Copyright
Copyright © Proprietors of Journal of Dairy Research 2013 

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References

Bach, AC & Barbayan, VK 1982 Medium-chain triglycerides: an update. American Journal of Clinical Nutrition 36 950962CrossRefGoogle ScholarPubMed
Barkema, HW, Van der Ploeg, JD, Schukken, YH, Lam, TJGM, Benedictus, G & Brands, A 1999 Management style and its association with bulk milk somatic cell count and incidence rate of clinical mastitis. Journal of Dairy Science 82 16551663Google Scholar
Bellinati-Pires, R, Waitzberg, DL, Salgado, MM & Carneiro-Sampaio, MMS 1993 Functional alterations of human neutrophils by medium-chain triglyceride emulsions – evaluation of phagocytosis, bacterial killing & oxidative activity. Journal of Leukocyte Biology 53 404410Google Scholar
Bernabucci, U, Ronchi, B, Lacetera, N & Nardone, A 2005 Influence of body condition score on relationships between metabolic status and oxidative stress in periparturient dairy cows. Journal of Dairy Science 88 20172026CrossRefGoogle ScholarPubMed
Bouwstra, RJ, Nielen, M, Stegeman, JA, Dobbelaar, P, Newbold, JR, Jansen, EHJM & van Werven, T 2010 Vitamin E supplementation during the dry period in dairy cattle. Part I: adverse effect on incidence of mastitis postpartum in a double-blind randomized field trial. Journal of Dairy Science 93 56845695CrossRefGoogle Scholar
Bradley, AJ & Green, MJ 2010 Managing dry cows to optimize udder health part I: understanding mammary gland susceptibility and the importance of the dry period in mastitis epidemiology. Irish Veterinary Journal 63 384387Google Scholar
Breckenridge, WC & Kuksis, A 1967 Molecular weight distributions of milk fat triglycerides from seven species. Journal of Lipid Research 8 473478Google Scholar
Castillo, C, Hernandez, J, Bravo, A, Lopez-Alonso, M, Pereira, V & Benedito, JL 2005 Oxidative status during late pregnancy and early lactation in dairy cows. Veterinary Journal 169 286292Google Scholar
Ceballos, A, Sanchez, J, Stryhn, H, Montgomery, JB, Barkema, HW & Wichtel, JJ 2009 Meta-analysis of the effect of oral selenium supplementation on milk selenium concentration in cattle. Journal of Dairy Science 92 324342Google Scholar
Dohme, F, Machmüller, A, Wasserfallen, A & Kreuzer, W 2000 Comparative efficiency of various fats rich in medium-chain fatty acids to suppress ruminal methanogenesis as measured with RUSITEC. Canadian Journal of Animal Science 80 473482CrossRefGoogle Scholar
Dohme, F, Machmüller, A, Wasserfallen, A & Kreuzer, M 2001 Ruminal methanogenesis as influenced by individual fatty acids supplemented to complete ruminant diets. Letters in Applied Microbiology 32 4751Google Scholar
Guidry, AJ, Paape, MJ & Pearson, RE 1976 Effects of parturition and lactation on blood and milk cell concentrations, corticosteroids and neutrophil phagocytosis in the cow. American Journal of Veterinary Research 37 11951200Google Scholar
Grummer, RR & Socha, MT 1989 Milk fatty-acid composition and plasma energy metabolite concentrations in lactating cows fed medium-chain triglycerides. Journal of Dairy Science 72 19962001Google Scholar
Henry, GE, Momin, RA, Nair, MG & Dewitt, DL 2002 Antioxidant and cyclooxygenase activities of fatty acids found in food. Journal of Agricultural and Food Chemistry 50 22312234Google Scholar
Kehrli, ME, Nonnecke, BJ & Roth, JA 1989 Alterations in bovine neutrophil function during periparturient period. American Journal of Veterinary Research 50 207214Google Scholar
Lemieux, H, Blier, PU & Tardif, J-C 2008 Does membrane fatty acid composition modulate mitochondrial functions and their thermal sensitivity? Comparative Biochemistry and Physiology Part A: Molecular and Integrative Physiology 149 2029Google Scholar
Lemieux, H, Bulteau, AL, Friguet, B, Tardif, J-C & Blier, PU 2011 Dietary fatty acids and oxidative stress in the heart mitochondria. Mitochondrion 11 97103Google Scholar
Mehrzad, J, Dosogne, H, Meyer, E, Heyneman, R & Burvenich, C 2001 Respiratory burst activity of blood and milk neutrophils in dairy cows during different stages of lactation. Journal of Dairy Research 68 399415Google Scholar
Mehrzad, J, Duchateau, L, Pyörälä, S & Burvenich, C 2002 Blood and milk neutrophil chemiluminescence and viability in primiparous and pluriparous dairy cows during late pregnancy, around parturition and early lactation. Journal of Dairy Science 85 32683276Google Scholar
Mehrzad, J, Duchateau, L & Burvenich, C 2004 Viability of milk neutrophils and severity of bovine coliform mastitis. Journal of Dairy Science 87 41504162CrossRefGoogle ScholarPubMed
Mehrzad, J, Duchateau, L & Burvenich, C 2005 High milk neutrophil chemiluminescence limits the severity of bovine coliform mastitis. Veterinary Research 36 101116Google Scholar
Nair, MKM, Joy, J, Vasudevan, P, Hinckley, L, Hoagland, TA & Venkitanarayanan, KS 2005 Antibacterial effect of caprylic acid and monocaprylin on major bacterial mastitis pathogens. Journal of Dairy Science 88 34883495CrossRefGoogle ScholarPubMed
Paape, MJ, Bannerman, DD, Zhao, X & Lee, JW 2003 The bovine neutrophil: structure and function in blood and milk. Veterinary Research 34 597627Google Scholar
Pantoja, JCF, Hulland, C & Ruegg, PL 2009 Somatic cell count across the dry period as a risk factor for the development of clinical mastitis in the subsequent lactation. Journal of Dairy Science 92 139148CrossRefGoogle ScholarPubMed
Piepers, S, De Meulemeester, L, de Kruif, A, Opsomer, G, Barkema, HW & De Vliegher, S 2007 Prevalence and distribution of mastitis pathogens in subclinically infected dairy cows in Flanders, Belgium. Journal of Dairy Research 74 478483Google Scholar
Piepers, S, De Vliegher, S, Demeyere, K, Lambrecht, BN, de Kruif, A, Meyer, E & Opsomer, G 2009a Technical Note: Flow cytometric identification of bovine milk neutrophils and simultaneous quantification of their viability. Journal of Dairy Science 92 626631Google Scholar
Piepers, S, Opsomer, G, Meyer, E, Demeyere, K, Barkema, HW, de Kruif, A & De Vliegher, S 2009b Heifer and quarter characteristics associated with periparturient blood and milk neutrophil apoptosis in healthy heifers and in heifers with subclinical mastitis. Journal of Dairy Science 92 43304339Google Scholar
Schukken, YH, Erb, HN, Sears, PM & Smith, RD 1988 Ecologic study of the risk factors for environmental mastitis in cows. American Journal of Veterinary Research 49 766769Google Scholar
Smith, KL, Todhunter, DA & Schoenberger, PS 1985 Environmental pathogens and intramammary infection during dry period. Journal of Dairy Science 68 402417Google Scholar
Sordillo, LM & Aitken, SL 2009 Impact of oxidative stress on the health and immune function of dairy cattle. Veterinary Immunology and Immunopathology 128 104109Google Scholar
Van Oostveldt, K, Dosogne, H, Burvenich, C, Paape, MJ, Brochez, V & Van den Eeckhout, E 1999a Flow cytometric procedure to detect apoptosis of bovine polymorphonuclear leukocytes in blood. Veterinary Immunology and Immunopathology 70 125133Google Scholar
Van Oostveldt, K, Burvenich, C, Paape, MJ & Meyer, E 1999b The effect of diapedesis on the apoptotic response of isolated bovine neutrophils. Cell Biology International 23 755791Google Scholar
Van Oostveldt, K, Vangroenweghe, F, Dosogne, H & Burvenich, C 2001 Apoptosis and necrosis of blood and milk polymorphonuclear leukocytes in early and midlactating healthy cows. Veterinary Research 32 617622Google Scholar
Van Oostveldt, K, Paape, MJ, Dosogne, H & Burvenich, C 2002 Effect of apoptosis on phagocytosis, respiratory burst and CD 18 adhesion receptor expression of bovine neutrophils. Domestic Animal Endocrinology 22 3750CrossRefGoogle Scholar
Vermes, I, Clemens, H, Steffens-Nakken, H & Reutelingsperger, C 1995 A novel assay for apoptotis flow cytometric detection of phosphatidylserine expression on early apoptotic cells using fluorescein labelled Annexin V. Journal of Immunological Methods 184 3951Google Scholar
Versleijen, M, Roelofs, H, Preijers, F, Roos, D & Wanten, G 2005 Parenteral lipids modulate leukocyte phenotypes in whole blood, depending on their fatty acid composition. Clinical Nutrition 24 822829Google Scholar
Versleijen, MWJ, van Esterik, JCJ, Roelofs, HMJ, van Ernst-de Vries, SE, Willems, PHGM & Wanten, GJA 2009 Parenteral medium-chain triglyceride-induced neutrophil activation is not mediated by a Pertussis toxin sensitive receptor. Clinical Nutrition 28 5964Google Scholar
Wanten, GJA, Janssen, FP & Naber, AHJ 2002 Saturated triglycerides and fatty acids activate neutrophils depending on carbon chain-length. European Journal of Clinical Investigation 32 285289CrossRefGoogle ScholarPubMed