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Effects of feed restriction and supplementary folic acid and vitamin B12 on immune cell functions and blood cell populations in dairy cows

Published online by Cambridge University Press:  10 October 2019

N. Vanacker
Affiliation:
Sherbrooke Research and Development Centre, Agriculture and Agri-Food Canada, 2000 College Sherbrooke, QC J1M 0C8, Canada Département de Biologie, Faculté des Sciences, Université de Sherbrooke, 2500 boulevard de l’Université,Sherbrooke, QC J1K 2R1, Canada
C. L. Girard
Affiliation:
Sherbrooke Research and Development Centre, Agriculture and Agri-Food Canada, 2000 College Sherbrooke, QC J1M 0C8, Canada
R. Blouin
Affiliation:
Département de Biologie, Faculté des Sciences, Université de Sherbrooke, 2500 boulevard de l’Université,Sherbrooke, QC J1K 2R1, Canada
P. Lacasse*
Affiliation:
Sherbrooke Research and Development Centre, Agriculture and Agri-Food Canada, 2000 College Sherbrooke, QC J1M 0C8, Canada
*
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Abstract

Cows undergoing a negative energy balance (NEB) often experience a state of immunosuppression and are at greater risk of infectious diseases. The present study aimed to evaluate the impact of a folic acid and vitamin B12 supplement and feed restriction on several immune parameters. Sixteen cows at 45 ± 3 days in milk were assigned to 8 blocks of 2 cows each according to each cow’s milk production in the previous week, and within each block, the cows randomly received weekly intramuscular injections of either saline or 320 mg of folic acid and 10 mg of vitamin B12 for 5 weeks. During week 5, the cows were fed 75% of their ad libitum intake for 4 days. Blood samples were taken before the beginning of the experiment, just before feed restriction and after 3 days of feed restriction, in order to evaluate blood cell populations, the phagocytosis capacity and oxidative burst of polymorphonuclear leukocytes (PMNs), the proliferation of peripheral blood mononuclear cells (PBMCs) and concentrations of non-esterified fatty acids (NEFAs) and β-hydroxybutyrate. The vitamin supplement did not affect any of the tested variables except milk fat and lactose content. Feed restriction reduced milk production and increased the concentration of NEFAs. Feed restriction did not affect blood cell populations but did reduce the percentage of PMN positive for oxidative burst after stimulation with phorbol 12-myristate 13-acetate. The proliferation of PBMCs was reduced when the cell culture medium was supplemented with sera collected during the feed restriction. In conclusion, feed restriction affected the functions of PMN and PBMC and this effect was not prevented by the folic acid and vitamin B12 supplement. These results support the hypothesis that the greater risk of infectious diseases in cows experiencing a NEB is related to impaired immune cell functions by high circulating concentration of NEFAs.

Type
Research Article
Copyright
© Her Majesty the Queen in Right of Canada, as represented by the Minister of Agriculture and Agri-Food Canada 2019 

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References

Bernier-Dodier, P, Girard, CL, Talbot, BG and Lacasse, P 2011. Effect of dry period management on mammary gland function and its endocrine regulation in dairy cows. Journal of Dairy Science 94, 49224936.CrossRefGoogle ScholarPubMed
Canadian Council on Animal Care 1993. Guide to the care and use of experimental animals, volume 1, 2nd edition. CCAC, Ottawa, ON, Canada.Google Scholar
Carbonneau, E, de Passillé, AM, Rushen, J, Talbot, BG and Lacasse, P 2012. The effect of incomplete milking or nursing on milk production, blood metabolites, and immune functions of dairy cows. Journal of Dairy Science 95, 65036512.CrossRefGoogle ScholarPubMed
Duplessis, M, Girard, CL, Santschi, DE, Laforest, J-P, Durocher, J and Pellerin, D 2014. Effects of folic acid and vitamin B12 supplementation on culling rate, diseases, and reproduction in commercial dairy herds. Journal of Dairy Science 97, 23462354.CrossRefGoogle ScholarPubMed
Duplessis, M, Lapierre, H, Pellerin, D, Laforest, J-P and Girard, CL 2017. Effects of intramuscular injections of folic acid, vitamin B12, or both, on lactational performance and energy status of multiparous dairy cows. Journal of Dairy Science 100, 40514064.CrossRefGoogle ScholarPubMed
Esposito, G, Irons, PC, Webb, EC and Chapwanya, A 2014. Interactions between negative energy balance, metabolic diseases, uterine health and immune response in transition dairy cows. Animal Reproduction Science 144, 6071.CrossRefGoogle ScholarPubMed
Gagnon, A, Khan, DR, Sirard, M-A, Girard, CL, Laforest, J-P and Richard, FJ 2015. Effects of intramuscular administration of folic acid and vitamin B12 on granulosa cells gene expression in postpartum dairy cows. Journal of Dairy Science 98, 77977809.CrossRefGoogle ScholarPubMed
Girard, C, Vanacker, N, Beaudet, V, Duplessis, M and Lacasse, P 2019. Glucose and insulin responses to an intravenous glucose tolerance test administered to fed-restricted dairy cows receiving folic acid and vitamin B12 supplements. Journal of Dairy Science 102, 62266234.CrossRefGoogle Scholar
Goff, JP and Horst, RL 1997. Physiological changes at parturition and their relationship to metabolic disorders. Journal of Dairy Science 80, 12601268.CrossRefGoogle ScholarPubMed
Graulet, B, Matte, JJ, Desrochers, A, Doepel, L, Palin, M-F and Girard, CL 2007. Effects of dietary supplements of folic acid and vitamin B12 on metabolism of dairy cows in early lactation. Journal of Dairy Science 90, 34423455.CrossRefGoogle ScholarPubMed
Hoeben, D, Burvenich, C, Trevisi, E, Bertoni, G, Hamann, J, Bruckmaier, RM and Blum, JW 2000. Role of endotoxin and TNF-α in the pathogenesis of experimentally induced coliform mastitis in periparturient cows. Journal of Dairy Research 67, 503514.CrossRefGoogle ScholarPubMed
Kehrli, ME Jr, Nonnecke, BJ and Roth, JA 1989. Alterations in bovine lymphocyte function during the periparturient period. American Journal of Veterinary Research 50, 215220.Google ScholarPubMed
Lacetera, N, Scalia, D, Bernabucci, U, Ronchi, B, Pirazzi, D and Nardone, A 2005. Lymphocyte functions in overconditioned cows around parturition. Journal of Dairy Science 88, 20102016.CrossRefGoogle ScholarPubMed
Leblanc, S 2010. Monitoring metabolic health of dairy cattle in the transition period. Journal of Reproduction and Development 56, S29S35.CrossRefGoogle ScholarPubMed
Leblanc, SJ, Lissemore, KD, Kelton, DF, Duffield, TF and Leslie, KE 2006. Major advances in disease prevention in dairy cattle. Journal of Dairy Science 89, 12671279.CrossRefGoogle ScholarPubMed
McGuire, MA, Theurer, M, Vicini, JL and Crooker, B 2004. Controlling energy balance in early lactation. Advances in Dairy Technology 16, 241252.Google Scholar
Moreira da Silva, F, Burvenich, C, Massart Leën, AM and Brossé, L 1998. Assessment of blood neutrophil oxidative burst activity in dairy cows during the period of parturition. Animal Science 67, 421426.CrossRefGoogle Scholar
National Research Council 2001. Nutrient requirements of dairy cattle 7th revue edition. National Academies Press, Washington, DC, USA.Google Scholar
Nonnecke, BJ, Kimura, K, Goff, JP and Kehrli, ME , Jr 2003. Effects of the mammary gland on functional capacities of blood mononuclear leukocyte populations from periparturient cows. Journal of Dairy Science 86, 23592368.CrossRefGoogle ScholarPubMed
Ollier, S, Beaudoin, F, Vanacker, N and Lacasse, P 2016. Effect of reducing milk production using a prolactin-release inhibitor or a glucocorticoid on metabolism and immune functions in cows subjected to acute nutritional stress. Journal of Dairy Science 99, 99499961.CrossRefGoogle ScholarPubMed
Ollier, S, Zhao, X and Lacasse, P 2014. Effects of feed restriction and prolactin-release inhibition at drying off on metabolism and mammary gland involution in cows. Journal of Dairy Science 97, 49424954.CrossRefGoogle ScholarPubMed
Preynat, A, Lapierre, H, Thivierge, MC, Palin, MF, Matte, JJ, Desrochers, A and Girard, CL 2009. Effects of supplements of folic acid, vitamin B12, and rumen-protected methionine on whole body metabolism of methionine and glucose in lactating dairy cows. Journal of Dairy Science 92, 677689.CrossRefGoogle ScholarPubMed
Roland, L, Drillich, M and Iwersen, M 2014. Hematology as a diagnostic tool in bovine medicine. Journal of Veterinary Diagnostic Investigation 26, 592598.CrossRefGoogle ScholarPubMed
Scott, JM 1999. Folate and vitamin B12 . Proceedings of Nutrition Society 58, 441448.CrossRefGoogle ScholarPubMed
Ster, C, Loiselle, M-C and Lacasse, P 2012. Effect of postcalving serum nonesterified fatty acids concentration on the functionality of bovine immune cells. Journal of Dairy Science 95, 708717.CrossRefGoogle ScholarPubMed
Vanacker, N, Girard, CL, Duplessis, M and Lacasse, P 2017b. Effects of supplementary folic acid and vitamin B12 feed-restriction on immune cell functions and blood cell population in dairy cows. Journal of Dairy Science 100 (suppl. 2), 277.Google Scholar
Vanacker, N, Ollier, S, Beaudoin, F, Blouin, R and Lacasse, P 2017a. Effect of inhibiting the lactogenic signal at calving on milk production and metabolic and immune perturbations in dairy cows. Journal of Dairy Science 100, 57825791.CrossRefGoogle ScholarPubMed
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