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Nutrition, immune function and health of dairy cattle

Published online by Cambridge University Press:  24 September 2012

K. L. Ingvartsen*
Affiliation:
Department of Animal Science, Aarhus University, Blichers Allé 20, PO Box 50, DK-8830 Tjele, Denmark
K. Moyes
Affiliation:
Department of Animal Science, Aarhus University, Blichers Allé 20, PO Box 50, DK-8830 Tjele, Denmark
*
E-mail: kli@agrsci.dk
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Abstract

The large increase in milk yield and the structural changes in the dairy industry have caused major changes in the housing, feeding and management of the dairy cow. However, while large improvements have occurred in production and efficiency, the disease incidence, based on veterinary records, does not seem to be improved. Earlier reviews have covered critical periods such as the transition period in the cow and its influence on health and immune function, the interplay between the endocrine system and the immune system and nutrition and immune function. Knowledge on these topics is crucial for our understanding of disease risk and our effort to develop health and welfare improving strategies, including proactive management for preventing diseases and reducing the severity of diseases. To build onto this the main purpose of this review will therefore be on the effect of physiological imbalance (PI) on immune function, and to give perspectives for prevention of diseases in the dairy cow through nutrition. To a large extent, the health problems during the periparturient period relate to cows having difficulty in adapting to the nutrient needs for lactation. This may result in PI, a situation where the regulatory mechanisms are insufficient for the animals to function optimally leading to a high risk of a complex of digestive, metabolic and infectious problems. The risk of infectious diseases will be increased if the immune competence is reduced. Nutrition plays a pivotal role in the immune response and the effect of nutrition may be directly through nutrients or indirectly by metabolites, for example, in situations with PI. This review discusses the complex relationships between metabolic status and immune function and how these complex interactions increase the risk of disease during early lactation. A special focus will be placed on the major energetic fuels currently known to be used by immune cells (i.e. glucose, non-esterified fatty acids, beta-hydroxybutyrate and glutamine) and how certain metabolic states, such as degree of negative energy balance and risk of PI, contribute to immunosuppression during the periparturient period. Finally, we will address some issues on disease prevention through nutrition.

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Copyright © The Animal Consortium 2012

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References

Allen, MS, Bradford, BJ, Oba, M 2009. Board Invited Review: the hepatic oxidation theory of the control of feed intake and its application to ruminants. Journal of Animal Science 87, 33173334.Google Scholar
Andersen, O 1991. Health control. Annual Report, National Committee on Danish Cattle Husbandry, Skejby, Denmark (In Danish), pp. 9–17.Google Scholar
Barghouthi, S, Everett, KD, Speert, DP 1995. Nonopsonic phagocytosis of Pseudomonas aeruginosa requires facilitated transport of d-glucose by macrophages. Journal of Immunology 154, 34203428.Google Scholar
Bastard, JP, Maachi, M, Lagathu, C, Kim, MJ, Caron, M, Vidal, H, Capeau, J, Feve, B 2006. Recent advances in the relationship between obesity, inflammation, and insulin resistance. European Cytokine Network 17, 412.Google Scholar
Bauman, DE 2000. Regulation of nutrient partitioning during lactation: homeostasis and homeorhesis revisited. In Ruminant physiology: digestion, metabolism, growth and reproduction (ed. PB Cronjé), pp. 311328. CABI Publishing, New York City, NY.Google Scholar
Bell, AW, Ehrhardt, RA 2000. Regulation of macronutrient partitioning between maternal and conceptus tissues in the pregnant ruminant. In Ruminant physiology: digestion, metabolism, growth and reproduction (ed. PB Cronjé), pp. 275293. CABI Publishing, New York City.CrossRefGoogle Scholar
Bell, AW, Slepetis, R, Ehrhardt, RA 1995. Growth and accretion of energy and protein in the gravid uterus during late pregnancy in Holstein cows. Journal of Dairy Science 78, 19541961.Google Scholar
Bertics, SJ, Grummer, RR, Cadorniga-Valino, C, Stoddard, EE 1992. Effect of prepartum dry matter intake on liver triglyceride concentration and early lactation. Journal of Dairy Science 75, 19141922.CrossRefGoogle ScholarPubMed
Brassard, P, Larbi, A, Grenier, A, Frisch, F, Fortin, C, Carpentier, AC, Fulop, T 2007. Modulation of T-cell signalling by non-esterified fatty acids. Prostaglandins, Leukotrienes and Essential Fatty Acids 77, 337343.Google Scholar
Bobe, G, Young, JW, Beitz, DC 2004. Invited review: pathology, etiology, prevention, and treatment of fatty liver in dairy cows. Journal of Dairy Science 87, 31053124.Google Scholar
Calder, PC, Bond, JA, Newsholme, EA 1990. Fatty acid inhibition of lipopolysaccharide-stimulated B lymphocyte proliferation. Biochemical SocietyTransactions 18, 904905.Google Scholar
Contreras, GA, Sordillo, LM 2011. Lipid mobilization and inflammatory responses during the transition period of dairy cows. Comparative Immunology, Microbiology and Infectious Diseases 34, 281289.Google Scholar
Dann, HM, Litherland, NB, Underwood, JP, Bionaz, M, D'Angelo, A, McFadden, JW, Drackley, JK 2006. Diets during far-off and close-up dry periods affect periparturient metabolism and lactation in multiparous cows. Journal of Dairy Science 89, 35633577.CrossRefGoogle ScholarPubMed
Detilleux, JC, Kehrli, ME Jr, Stabel, JR, Freeman, AE, Kelley, DH 1995. Study of immunological dysfunction in periparturient Holstein cattle selected for high and average milk production. Veterinary Immunology and Immunopathology 44, 251267.CrossRefGoogle ScholarPubMed
Doepel, L, Lessard, M, Gagnon, N, Lobley, GE, Bernier, JF, Dubreuil, P, Lapierre, H 2006. Effect of postruminal glutamine supplementation on immune response and milk production in dairy cows. Journal of Dairy Science 89, 31073121.CrossRefGoogle ScholarPubMed
Douglas, GN, Overton, TR, Bateman, HG, Dann, HM, Drackley, JK 2006. Prepartal plane of nutrition, regardless of dietary energy source, affects periparturient metabolism and dry matter intake in Holstein cows. Journal of Dairy Science 89, 21412157.CrossRefGoogle ScholarPubMed
Douglas, GN, Rehage, J, Beaulieu, AD, Bahaa, AO, Drackley, JK 2007. Prepartum nutrition alters fatty acid composition in plasma, adipose tissue, and liver lipids of periparturient dairy cows. Journal of Dairy Science 90, 29412959.Google Scholar
Drackley, JK, Donkin, SS, Reynolds, CK 2006. Major advances in fundamental dairy cattle nutrition. Journal of Dairy Science 89, 13241336.CrossRefGoogle ScholarPubMed
Duffield, TF, Lissemore, KD, McBride, BW, Leslie, KE 2009. Impact of hyperketonemia in early lactation dairy cows on health and production. Journal of Dairy Science 92, 571580.Google Scholar
Enevoldsen, C, Sorensen, JT 1992. Effects of dry period length on clinical mastitis and other major clinical health disorders. Journal of Dairy Science 75, 10071014.CrossRefGoogle ScholarPubMed
Franklin, ST, Young, JW, Nonnecke, BJ 1991. Effects of ketones, acetate, butyrate, and glucose on bovine lymphocyte proliferation. Journal of Dairy Science 74, 25072514.CrossRefGoogle ScholarPubMed
Friggens, NC, Andersen, JB, Larsen, T, Aaes, O, Dewhurst, RJ 2004a. Priming the dairy cow for lactation: a review of dry cow feeding strategies. Animal Research 53, 453473.Google Scholar
Friggens, NC, Ingvartsen, KL, Emmans, GC 2004b. Prediction of body lipid change in pregnancy and lactation. Journal of Dairy Science 87, 9881000.Google Scholar
Fukuzumi, M, Shinomiya, H, Shimizu, Y, Ohishi, K, Utsumi, S 1996. Endotoxin-induced enhancement of glucose influx into murine peritoneal macrophages via GLUT1. Infection and Immunity 64, 108112.Google Scholar
Furukawa, S, Saito, H, Inoue, T, Matsuda, T, Fukatsu, K, Han, I, Ikeda, S, Hidemura, A 2000. Supplemental glutamine augments phagocytosis and reactive oxygen intermediate production by neutrophils and monocytes from postoperative patients in vitro. Nutrition 16, 323329.Google Scholar
Gamelli, RL, Liu, H, He, LK, Hofmann, CA 1996. Augmentations of glucose uptake and glucose transporter-1 in macrophages following thermal injury and sepsis in mice. Journal of Leukocyte Biology 59, 639647.Google Scholar
Goff, JP 2006. Major advances in our understanding of nutritional influences on bovine health. Journal of Dairy Science 89, 12921301.Google Scholar
Gorjão, R, Verlengia, R, Lima, TM, Soriano, FG, Boaventura, MF, Kanunfre, CC, Peres, CM, Sampaio, SC, Otton, R, Folador, A, Martins, EF, Curi, TC, Portiolli, EP, Newsholme, P, Curi, R 2006. Effect of docosahexaenoic acid-rich fish oil supplementation on human leukocyte function. Clinical Nutrition 25, 923938.Google Scholar
Grummer, RR 1993. Etiology of lipid-related metabolic disorders in periparturient dairy cows. Journal of Dairy Science 76, 38823896.Google Scholar
Hansen, JV, Friggens, NC, Hojsgaard, S 2006. The influence of breed and parity on milk yield, and milk yield acceleration curves. Livestock Science 104, 5362.Google Scholar
Hayirli, A, Grummer, RR, Nordheim, EV, Crump, PM 2002. Animal and dietary factors affecting feed intake during the prefresh transition period in Holsteins. Journal of Dairy Science 85, 34303443.CrossRefGoogle ScholarPubMed
Herdt, TH 2000. Ruminant adaptation to negative energy balance. Influences on the etiology of ketosis and fatty liver. Veterinary Clinics of North America: Food Animal Practice 16, 215230.Google Scholar
Hoeben, D, Heyneman, R, Burvenich, C 1997. Elevated levels of beta-hydroxybutyric acid in periparturient cows and in vitro effect on respiratory burst activity of bovine neutrophils. Veterinary Immunology and Immunopathology 58, 165170.Google Scholar
Holtenius, K, Persson, WK, Essen-Gustavsson, B, Holtenius, P, Hallen, SC 2004. Metabolic parameters and blood leukocyte profiles in cows from herds with high or low mastitis incidence. Veterinary Journal 168, 6573.CrossRefGoogle ScholarPubMed
Hughes, DA, Pinder, AC 2000. n-3 polyunsaturated fatty acids inhibit the antigen-presenting function of human monocytes. American Journal of Clinical Nutrition 71 (suppl. S), 357S360S.Google Scholar
Ingvartsen, KL 2006. Feeding and management related diseases in the transition cow. Physiological adaptations around calving and strategies to reduce feeding-related diseases. Animal Feed Science and Technology 126, 175213.Google Scholar
Ingvartsen, KL, Andersen, JB 2000. Integration of metabolism and intake regulation: a review focusing on periparturient animals. Journal of Dairy Science 83, 15731597.Google Scholar
Ingvartsen, KL, Boisclair, YR 2001. Leptin and the regulation of food intake, energy homeostasis and immunity with special focus on periparturient ruminants. Domestic Animal Endocrinology 21, 215250.Google Scholar
Ingvartsen, KL, Dewhurst, RJ, Friggens, NC 2003. On the relationship between lactational performance and health: is it yield or metabolic imbalance that cause production diseases in dairy cattle? A position paper. Livestock Production Science 83, 277308.Google Scholar
Janosi, S, Kulcsar, M, Korodi, P, Katai, L, Reiczigel, J, Dieleman, SJ, Nikolic, JA, Salyi, G, Ribiczey-Szabo, P, Huszenicza, G 2003. Energy imbalance related predisposition to mastitis in group-fed high-producing postpartum dairy cows. Acta Veterinaria Hungarica 51, 409424.Google Scholar
Janovick, NA, Boisclair, YR, Drackley, JK 2011. Prepartum dietary energy intake affects metabolism and health during the periparturient period in primiparous and multiparous Holstein cows. Journal of Dairy Science 94, 13851400.CrossRefGoogle ScholarPubMed
Janovick-Guretzky, NA, Dann, HM, Carlson, DB, Murphy, MR, Loor, JJ, Drackley, JK 2007. Housekeeping gene expression in bovine liver is affected by physiological state, feed intake, and dietary treatment. Journal of Dairy Science 90, 22462252.Google Scholar
Kehrli, ME JrHarp, JA 2001. Immunity in the mammary gland. Veterinary Clinics of North America: Food Animal Practice 17, 495516.Google Scholar
Kehrli, ME, Neill, JD, Burvenich, C, Goff, JP, Lippolis, JDRTA, Nonnecke, BJ 2006. Energy and protein effects on the immune system. In Ruminant physiology. Digestion, metabolism and impact of nutrition on gene expression, immunology and stress (ed. K Sejrsen, T Hvelplund and MO Nielsen), pp. 455471. Wageningen Academic Publishers, Wageningen, The Netherlands.Google Scholar
Kelton, DF, Lissemore, KD, Martin, RE 1998. Recommendations for recording and calculating the incidence of selected clinical diseases of dairy cattle. Journal of Dairy Science 81, 25022509.Google Scholar
Klucinski, W, Degorski, A, Miernik-Degorska, E, Targowski, S, Winnicka, A 1988. Effect of ketone bodies on the phagocytic activity of bovine milk macrophages and polymorphonuclear leukocytes. Zentralblatt fur Veterinarmedizin A 35, 632639.Google ScholarPubMed
Kremer, WD, Noordhuizen-Stassen, EN, Grommers, FJ, Schukken, YH, Heeringa, R, Brand, A, Burvenich, C 1993. Severity of experimental Escherichia coli mastitis in ketonemic and nonketonemic dairy cows. Journal of Dairy Science 76, 34283436.Google Scholar
Krogh, K, Tinderup, M 2008. Ny opgørelse over sygdomsbehandlinger i mælkekvægsbesætninger [New calculation of disease treatments in dairy herds]. Kvæginfo 1902. Videncentret for Landbrug, Aarhus, Denmark (In Danish).Google Scholar
Lacetera, N, Scalia, D, Franci, O, Bernabucci, U, Ronchi, B, Nardone, A 2004. Short communication: effects of nonesterified fatty acids on lymphocyte function in dairy heifers. Journal of Dairy Science 87, 10121014.Google Scholar
Lacetera, N, Scalia, D, Bernabucci, U, Ronchi, B, Pirazzi, D, Nardone, A 2005. Lymphocyte functions in overconditioned cows around parturition. Journal of Dairy Science 88, 20102016.Google Scholar
Lang, CH, Dobrescu, C 1991. Sepsis-induced increases in glucose uptake by macrophage-rich tissues persist during hypoglycemia. Metabolism 40, 585593.Google Scholar
Law, RA, Young, FJ, Patterson, DC, Kilpatrick, DJ, Wylie, AR, Ingvarsten, KL, Hameleers, A, McCoy, MA, Mayne, CS, Ferris, C 2011. Effect of precalving and postcalving dietary energy level on performance and blood metabolite concentrations of dairy cows throughout lactation. Journal of Dairy Science 94, 808823.Google Scholar
LeBlanc, SJ, Leslie, KE, Duffield, TF 2005. Metabolic predictors of displaced abomasum in dairy cattle. Journal of Dairy Science 88, 159170.Google Scholar
Lee, JY, Hwang, DH 2006. The modulation of inflammatory gene expression by lipids: mediation through Toll-like receptors. Molecules and Cells 21, 174185.Google Scholar
Lee, JY, Plakidas, A, Lee, WH, Heikkinen, A, Chanmugam, P, Bray, G, Hwang, DH 2003. Differential modulation of Toll-like receptors by fatty acids: preferential inhibition by n-3 polyunsaturated fatty acids. Journal of Lipid Research 44, 479486.Google Scholar
Lee, JY, Zhao, L, Youn, HS, Weatherill, AR, Tapping, R, Feng, L, Lee, WH, Fitzgerald, KA, Hwang, DH 2004. Saturated fatty acid activates but polyunsaturated fatty acid inhibits Toll-like receptor 2 dimerized with Toll-like receptor 6 or 1. Journal of Biological Chemistry 279, 1697116979.CrossRefGoogle ScholarPubMed
Liu, GW, Zhang, ZG, Wang, JG, Wang, Z, Xu, C, Zhu, XL 2010. Insulin receptor gene expression in normal and diseased bovine liver. Journal of Comparative Pathology 143, 258261.Google Scholar
Loor, JJ, Dann, HM, Everts, RE, Oliveira, R, Green, CA, Guretzky, NA, Rodriguez-Zas, SL, Lewin, HA, Drackley, JK 2005. Temporal gene expression profiling of liver from periparturient dairy cows reveals complex adaptive mechanisms in hepatic function. Physiological Genomics 23, 217226.Google Scholar
Markusfeld, O, Galon, N, Ezra, E 1997. Body condition score, health, yield and fertility in diary cows. Veterinary Record 141, 6772.Google Scholar
McCarthy, SD, Waters, SM, Kenny, DA, Diskin, MG, Fitzpatrick, R, Patton, J, Wathes, DC, Morris, DG 2010. Negative energy balance and hepatic gene expression patterns in high-yielding dairy cows during the early postpartum period: a global approach. Physiological Genomics 42A, 188199.Google 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, 399415.Google Scholar
Meinz, H, Lacy, DB, Ejiofor, J, McGuinness, OP 1998. Alterations in hepatic gluconeogenic amino acid uptake and gluconeogenesis in the endotoxin treated conscious dog. Shock 9, 296303.Google Scholar
Miles, EA, Banerjee, T, Wells, SJ, Calder, PC 2006. Limited effect of eicosapentaenoic acid on T-lymphocyte and natural killer cell numbers and functions in healthy young males. Nutrition 22, 512519.Google Scholar
Morris, DG, Waters, SM, McCarthy, SD, Patton, J, Earley, B, Fitzpatrick, R, Murphy, JJ, Diskin, MG, Kenny, DA, Brass, A, Wathes, DC 2009. Pleiotropic effects of negative energy balance in the postpartum dairy cow on splenic gene expression: repercussions for innate and adaptive immunity. Physiological Genomics 39, 2837.Google Scholar
Moyes, KM, Drackley, JK, Morin, DE, Loor, JJ 2010a. Greater expression of TLR2, TLR4, and IL6 due to negative energy balance is associated with lower expression of HLA-DRA and HLA-A in bovine blood neutrophils after intramammary mastitis challenge with Streptococcus uberis. Functional and Integrative Genomics 10, 5361.Google Scholar
Moyes, KM, Drackley, JK, Morin, DE, Rodriguez-Zas, SL, Everts, RE, Lewin, HA, Loor, JJ 2010b. Mammary gene expression profiles during an intramammary challenge reveal potential mechanisms linking negative energy balance with impaired immune response. Physiological Genomics 41, 161170.Google Scholar
Moyes, KM, Drackley, JK, Salak-Johnson, JL, Morin, DE, Hope, JC, Loor, JJ 2009a. Dietary-induced negative energy balance has minimal effects on innate immunity during a Streptococcus uberis mastitis challenge in dairy cows during midlactation. Journal of Dairy Science 92, 43014316.CrossRefGoogle ScholarPubMed
Moyes, KM, Larsen, T, Friggens, NC, Drackley, JK, Ingvartsen, KL 2009b. Identification of potential markers in blood for the development of subclinical and clinical mastitis in dairy cattle at parturition and during early lactation. Journal of Dairy Science 92, 54195428.Google Scholar
Mukesh, M, Bionaz, M, Graugnard, DE, Drackley, JK, Loor, JJ 2010. Adipose tissue depots of Holstein cows are immune responsive: inflammatory gene expression in vitro. Domestic Animal Endocrinology 38, 168178.Google Scholar
Mulligan, FJ, Doherty, ML 2008. Production diseases of the transition cow. Veterinary Journal 176, 39.Google Scholar
National Research Council. 2001. Nutrient requirements of dairy cattle. National Academy Press, Washington, DC.Google Scholar
Newsholme, EA, Crabtree, B, Ardawi, MS 1985. Glutamine metabolism in lymphocytes: its biochemical, physiological and clinical importance. Quarterly Journal of Experimental Physiology 70, 473489.Google Scholar
Newsholme, P, Gordon, S, Newsholme, EA 1987. Rates of utilization and fates of glucose, glutamine, pyruvate, fatty acids and ketone bodies by mouse macrophages. Biochemistry Journal 242, 631636.CrossRefGoogle ScholarPubMed
Newsholme, P, Curi, R, Gordon, S, Newsholme, EA 1986. Metabolism of glucose, glutamine, long-chain fatty acids and ketone bodies by murine macrophages. Biochemical Journal 239, 121125.Google Scholar
Newsholme, P, Curi, R, Pithon Curi, TC, Murphy, CJ, Garcia, C, Pires de, MM 1999. Glutamine metabolism by lymphocytes, macrophages, and neutrophils: its importance in health and disease. Journal of Nutritional Biochemistry 10, 316324.CrossRefGoogle ScholarPubMed
Nonnecke, BJ, Franklin, ST, Young, JW 1992. Effects of ketones, acetate, and glucose on in vitro immunoglobulin secretion by bovine lymphocytes. Journal of Dairy Science 75, 982990.CrossRefGoogle ScholarPubMed
Ogle, CK, Ogle, JD, Mao, JX, Simon, J, Noel, JG, Li, BG, Alexander, JW 1994. Effect of glutamine on phagocytosis and bacterial killing by normal and pediatric burn patient neutrophils. Journal of Parental and Enteral Nutrition 18, 128133.Google Scholar
Paape, MJ, Guidry, AJ, Jain, NC, Miller, RH 1991. Leukocytic defense mechanisms in the udder. Flemish Veterinary Journal 62 (suppl. 1), 95109.Google Scholar
Perkins, KH, VandeHaar, MJ, Tempelman, RJ, Burton, JL 2001. Negative energy balance does not decrease expression of leukocyte adhesion or antigen-presenting molecules in cattle. Journal of Dairy Science 84, 421428.Google Scholar
Perkins, KH, VandeHaar, MJ, Burton, JL, Liesman, JS, Erskine, RJ, Elsasser, TH 2002. Clinical responses to intramammary endotoxin infusion in dairy cows subjected to feed restriction. Journal of Dairy Science 85, 17241731.Google Scholar
Pezeshki, A, Capuco, AV, De Spiegeleer, B, Peelman, L, Stevens, M, Collier, RJ, Burvenich, C 2010. An integrated view on how the management of the dry period length of lactating cows could affect mammary biology and defense. Journal of Animal Physiology and Animal Nutrition 94, e7e30.CrossRefGoogle Scholar
Pithon-Curi, TC, De Melo, MP, Curi, R 2004. Glucose and glutamine utilization by rat lymphocytes, monocytes and neutrophils in culture: a comparative study. Cell Biochemistry and Function 22, 321326.CrossRefGoogle ScholarPubMed
Quiroz-Rocha, GF, LeBlanc, S, Duffield, T, Wood, D, Leslie, KE, Jacobs, RM 2009. Evaluation of prepartum serum cholesterol and fatty acids concentrations as predictors of postpartum retention of the placenta in dairy cows. Journal of the American Veterinary Medical Association 234, 790793.Google Scholar
Rainard, P, Riollet, C 2006. Innate immunity of the bovine mammary gland. Veterinary Research 37, 369400.Google Scholar
Rastani, RR, Andrew, SM, Zinn, SA, Sniffen, CJ 2001. Body composition and estimated tissue energy balance in Jersey and Holstein cows during early lactation. Journal of Dairy Science 84, 12011209.Google Scholar
Rezamand, P, McGuire, MA 2011. Effects of trans fatty acids on markers of inflammation in bovine mammary epithelial cells. Journal of Dairy Science 94, 316320.Google Scholar
Sartorelli, P, Paltrinieri, S, Agnes, F 1999. Non-specific immunity and ketone bodies. I: In vitro studies on chemotaxis and phagocytosis in ovine neutrophils. Zentralblatt fur Veterinarmedizin A 46, 613619.Google Scholar
Sato, S, Suzuki, T, Okada, K 1995. Suppression of mitogenic response of bovine peripheral blood lymphocytes by ketone bodies. Journal of Veterinary Medical Science 57, 183185.Google Scholar
Scalia, D, Lacetera, N, Bernabucci, U, Demeyere, K, Duchateau, L, Burvenich, C 2006. In vitro effects of nonesterified fatty acids on bovine neutrophils oxidative burst and viability. Journal of Dairy Science 89, 147154.Google Scholar
Schuster, DP, Brody, SL, Zhou, Z, Bernstein, M, Arch, R, Link, D, Mueckler, M 2007. Regulation of lipopolysaccharide-induced increases in neutrophil glucose uptake. American Journal of Physiology – Lung Cellular and Molecular Physiology 292, L845L851.Google Scholar
Shi, H, Kokoeva, MV, Inouye, K, Tzameli, I, Yin, H, Flier, JS 2006. TLR4 links innate immunity and fatty acid-induced insulin resistance. Journal of Clinical Investigation 116, 30153025.Google Scholar
Sordillo, LM, Aitken, SL 2009. Impact of oxidative stress on the health and immune function of dairy cattle. Veterinary Immunology and Immunopathology 128, 104109.Google Scholar
Sordillo, LM, Shafer-Weaver, K, DeRosa, D 1997. Immunobiology of the mammary gland. Journal of Dairy Science 80, 18511865.Google Scholar
Sordillo, LM, Contreras, GA, Aitken, SL 2009. Metabolic factors affecting the inflammatory response of periparturient dairy cows. Animal Health Research Reviews 10, 5363.Google Scholar
Sorensen, JT, Enevoldsen, C 1991. Effect of dry period length on milk production in subsequent lactation. Journal of Dairy Science 74, 12771283.Google Scholar
Stevens, MG, Peelman, LJ, De, SB, Pezeshki, A, Van De Walle, GR, Duchateau, L, Burvenich, C 2011. Differential gene expression of the toll-like receptor-4 cascade and neutrophil function in early- and mid-lactating dairy cows. Journal of Dairy Science 94, 12771288.Google Scholar
Suriyasathaporn, W, Heuer, C, Noordhuizen-Stassen, EN, Schukken, YH 2000. Hyperketonemia and the impairment of udder defense: a review. Veterinary Research 31, 397412.Google Scholar
Suriyasathaporn, W, Daemen, AJ, Noordhuizen-Stassen, EN, Dieleman, SJ, Nielen, M, Schukken, YH 1999. Beta-hydroxybutyrate levels in peripheral blood and ketone bodies supplemented in culture media affect the in vitro chemotaxis of bovine leukocytes. Veterinary Immunology and Immunopathology 68, 177186.Google Scholar
Targowski, SP, Klucinski, W 1983. Reduction in mitogenic response of bovine lymphocytes by ketone bodies. American Journal of Veterinary Research 44, 828830.Google Scholar
Tilg, H, Moschen, AR 2008. Insulin resistance, inflammation, and non-alcoholic fatty liver disease. Trends in Endocrinology and Metabolism 19, 371379.Google Scholar
Trebble, T, Arden, NK, Stroud, MA, Wootton, SA, Burdge, GC, Miles, EA, Ballinger, AB, Thompson, RL, Calder, PC 2003a. Inhibition of tumour necrosis factor-alpha and interleukin 6 production by mononuclear cells following dietary fish-oil supplementation in healthy men and response to antioxidant co-supplementation. British Journal of Nutrition 90, 405412.Google Scholar
Trebble, TM, Wootton, SA, Miles, EA, Mullee, M, Arden, NK, Ballinger, AB, Stroud, MA, Burdge, GC, Calder, PC 2003b. Prostaglandin E2 production and T cell function after fish-oil supplementation: response to antioxidant cosupplementation. American Journal of Clinical Nutrition 78, 376382.Google Scholar
Trinderup, M, Kjeldsen, AM, Andersen, O 2001. Forskellige behandlingsfrekvenser af malkekøer i forskellige staldsystemer [Different treatment frequency of dairy cows in different housing systems]. LK-meddelelse 905, 18 (In Danish).Google Scholar
Vangroenweghe, F, Lamote, I, Burvenich, C 2005. Physiology of the periparturient period and its relation to severity of clinical mastitis. Domestic Animal Endocrinology 29, 283293.Google Scholar
Vernon, RG 2005. Lipid metabolism during lactation: a review of adipose tissue-liver interactions and the development of fatty liver. Journal of Dairy Research 72, 460469.Google Scholar
Wallace, C, Keast, D 1992. Glutamine and macrophage function. Metabolism 41, 10161020.Google Scholar
Wathes, DC, Cheng, Z, Chowdhury, W, Fenwick, MA, Fitzpatrick, R, Morris, DG, Patton, J, Murphy, JJ 2009. Negative energy balance alters global gene expression and immune responses in the uterus of postpartum dairy cows. Physiological Genomics 39, 113.Google Scholar
Yassad, A, Lavoinne, A, Bion, A, Daveau, M, Husson, A 1997. Glutamine accelerates interleukin-6 production by rat peritoneal macrophages in culture. Federation of European Biochemical Societies Letters 413, 8184.Google Scholar