Metabolism and immune status during transition period influences the lactation performance in Zebu (Bos indicus) cows


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Authors

  • PRATIK RAMESH WANKHADE Research Scholar, Southern Regional Station, ICAR-National Dairy Research Institute, Adugodi, Bengaluru Karnataka 560 030 India
  • AYYASAMY MANIMARAN Scientist, Southern Regional Station, ICAR-National Dairy Research Institute, Adugodi, Bengaluru Karnataka 560 030 India
  • ARUMUGAM KUMARESAN Principal Scientist, Livestock Research Centre (LRC), Southern Regional Station, ICAR-National Dairy Research Institute, Adugodi, Bengaluru Karnataka 560 030 India
  • SAKTHIVEL JEYAKUMAR Principal Scientist, Livestock Research Centre (LRC), Southern Regional Station, ICAR-National Dairy Research Institute, Adugodi, Bengaluru Karnataka 560 030 India
  • KEREKOPPA P RAMESHA Principal Scientist and Head, Southern Regional Station, ICAR-National Dairy Research Institute, Adugodi, Bengaluru Karnataka 560 030 India
  • VEERASAMY SEJIAN Senior Scientist, Division of Animal Physiology, Southern Regional Station, ICAR-National Dairy Research Institute, Adugodi, Bengaluru Karnataka 560 030 India
  • DURAISAMY RAJENDRAN Principal Scientist, Division of Animal Nutrition, ICAR-National Institute of Animal Nutrition and Physiology, Adugodi, Bengaluru, Karnataka.
  • MADIAJAGAN BAGATH Scientist, Division of Animal Nutrition, ICAR-National Institute of Animal Nutrition and Physiology, Adugodi, Bengaluru, Karnataka
  • MUNIANDY SIVARAM Senior Scientist, Southern Regional Station, ICAR-National Dairy Research Institute, Adugodi, Bengaluru Karnataka 560 030 India

https://doi.org/10.56093/ijans.v88i9.83556

Keywords:

Acute phase proteins, Deoni cows, Energy indicators, Inflammatory cytokines, Milk yield, Transition period

Abstract

We evaluated the changes in the concentration of innate immune molecules (haptoglobin: Hp, serum amyloid A: SAA, IL-6, TNF-α, IL-1β, and IL-8), energy indicators [NEFA, dry matter intake (DMI) and body condition scoring (BCS)] during the transition period in dual-purpose Zebu (Deoni breed) cows in relation to milk yield. Blood collection was done at weekly intervals (–21±2, –14±1, –7±1, d pre-partum, day 0 (date of calving) and 3±1, 7±1, 14±1, 21±2 d postpartum period) for estimation of above plasma variables using commercially available bovine specific ELISA kits. We also recorded DMI and BCS during the corresponding period. Transition cows were classified based on their milk yield during the study period as high (6), medium (6) and low (6) yielding cows and data were analyzed by using Mixed-model repeated measure analysis. High yielding (HY) cows had significantly higher concentrations of SAA, TNF-α, and IL-6 during pre-partum and early postpartum period than low yielding (LY) cows. DMI was significantly higher in HY cows than MY (3rd and 7th d) or LY cows (21st d) while, BCS was significantly higher in HY than LY cows during pre-partum period (-7th d). LY cows had significantly higher concentration of NEFA during the postpartum period (14th and 21st d). It is concluded that the active functioning of the immune system and more dry matter intake in transition Deoni cows enabled to synthesise more milk during the postpartum period.

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References

Adewuyi A A, Gruys E and Van Eerdenburg F J C M. 2005. Non esterified fatty acids (NEFA) in dairy cattle. A review. Veterinary Quarterly 27(3): 117–26. DOI: https://doi.org/10.1080/01652176.2005.9695192

Aitken S L, Corl C M and Sordillo L M. 2011. Immunopathology of mastitis: insights into disease recognition and resolution. Journal of Mammary Gland Biology and Neoplasia 16(4): 291–304. DOI: https://doi.org/10.1007/s10911-011-9230-4

Banos G, Wall E, Coffey M P, Bagnall A, Gillespie S, Russell G C and McNeilly T N. 2013. Identification of immune traits correlated with dairy cow health, reproduction and productivity. PLoS ONE 8(6): 65766. DOI: https://doi.org/10.1371/journal.pone.0065766

Bionaz M, Trevisi E, Calamari L U I G I, Librandi F, Ferrari A and Bertoni G. 2007. Plasma paraoxonase, health, inflammatory conditions, and liver function in transition dairy cows. Journal of Dairy Science 90(4): 1740–50. DOI: https://doi.org/10.3168/jds.2006-445

Das D N, Kataktalware M A, Ramesha K P and Reddy A O. 2011. Productive and reproductive performances of Deoni cattle under intensive management system. Indian Journal of Animal Sciences 81: 11.

Duffield T F and LeBlanc S J. 2009. Interpretation of serum metabolic parameters around the transition period. Southwest Nutrition and Management Conference, Ontario Veterinary College, Guelph, pp 106–114.

El-Deeb W M and El-Bahr S M. 2017. Biomarkers of ketosis in dairy cows at postparturient period: acute phase proteins and pro-inflammatory cytokines. Veterinarski Arhiv 87(4): 431– 40. DOI: https://doi.org/10.24099/vet.arhiv.160126c

Farney J K, Mamedova L K, Coetzee J F, KuKanich B, Sordillo L M, Stoakes S K, Minton J E, Hollis L C and Bradford B J. 2013. Anti-inflammatory salicylate treatment alters the metabolic adaptations to lactation in dairy cattle. American Journal of Physiology-Regulatory, Integrative and Comparative Physiology 305(2): 110–17. DOI: https://doi.org/10.1152/ajpregu.00152.2013

Gabler C, Fischer C, Drillich M, Einspanier R and Heuwieser W. 2010. Time-dependent mRNA expression of selected proinflammatory factors in the endometrium of primiparous cows postpartum. Reproductive Biology and Endocrinology 8(1): 152. DOI: https://doi.org/10.1186/1477-7827-8-152

Gruffat D, Durand D, Graulet B and Bauchart D. 1996. Regulation of VLDL synthesis and secretion in the liver. Reproduction Nutrition Development 36: 375–89. DOI: https://doi.org/10.1051/rnd:19960404

Herdt T H. 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: 215–30. DOI: https://doi.org/10.1016/S0749-0720(15)30102-X

International Dairy Federation (IDF). 1991. International provisional IDF standard 152. Milk and Milk products. Determination of fat content. General guidance on the use of butyrometric methods. Brussels, Belgium.

Jílek F, Pytloun P, Kubešová M, Štípková M, Bouška J, Volek J, Frelich J and Rajmon R. 2008. Relationships among body condition score, milk yield and reproduction in Czech Fleckvieh cows. Czech Journal of Animal Science 53(9): 357– 67. DOI: https://doi.org/10.17221/335-CJAS

Kerhli M E. 2015. Immunological dysfunction in periparturient cows: evidence, causes and ramifications. Proceeding Florida Nutrition Conference 1: 14–29.

Kellog W. 2010. Body Condition Scoring with Dairy Cattle. University of Arkansas, United States Department of Agriculture and County Governments Cooperating. Available at https://www.uaex.edu/publications/pdf/FSA-4008.pdf. Accessed 5 July 2017.

Kovac G, Tothova C, Nagy O, Seidel H and Konvicna J. 2009. Acute phase proteins and their relation to energy metabolites in dairy cows during the pre-and postpartal period. Acta Veterinaria Brno 78(3): 441–47. DOI: https://doi.org/10.2754/avb200978030441

Kushibiki S, Hodate K, Shingu H, Ueda Y, Mori Y, Itoh T and Yokomizo Y. 2001. Effects of long-term administration of recombinant bovine tumor necrosis factor-α on glucose metabolism and growth hormone secretion in steers. American Journal of Veterinary Research 62(5): 794–98. DOI: https://doi.org/10.2460/ajvr.2001.62.794

LeBlanc S. 2010. Monitoring metabolic health of dairy cattle in the transition period. Journal of Reproduction and Development 56(S): 29–35. DOI: https://doi.org/10.1262/jrd.1056S29

LeBlanc S. 2013. Managing critical periods-transition dairy cows. Book of Abstracts, 15th Conference on Production Diseases in Farm Animals. (Ed) Dalin G. Swedish University of Agricultural Science, Uppsala, Sweden. p 62–65.

Loor J J, Dann H M, Everts R E, Oliveira R, Green C A, Guretzky N A J, Rodriguez-Zas S L, Lewin H A and Drackley J K. 2005. Temporal gene expression profiling of liver from periparturient dairy cows reveals complex adaptive mechanisms in hepatic function. Physiological Genomics 23(2): 217–26. DOI: https://doi.org/10.1152/physiolgenomics.00132.2005

Majkic M, Cincovic M R, Belic B, Plavsa N, Lakic I and Radinovic M. 2017. Relationship between milk production and metabolic adaptation in dairy cows during heat stress. Acta Agriculturae Serbica 44: 123–31. DOI: https://doi.org/10.5937/AASer1744123M

Mathews A T, Rico J E, Sprenkle N T, Lock A L and McFadden J W. 2016. Increasing palmitic acid intake enhances milk production and prevents glucose-stimulated fatty acid disappearance without modifying systemic glucose tolerance in mid-lactation dairy cows. Journal of Dairy Science 99(11): 8802–16. DOI: https://doi.org/10.3168/jds.2016-11295

McLean D. 2017. Immunity in dairy cattle: what’s a healthy cow? Available at https://ecommons.cornell.edu/bitstream/handle/ 1813/53362/Pre1_McLean_manu.pdf?sequence=1. Accessed on 27 January 2018.

Moe P W, Tyrrell H F and Flatt W P. 1971. Energetics of body tissue mobilization. Journal of Dairy Science 54(4): 548–53. DOI: https://doi.org/10.3168/jds.S0022-0302(71)85886-1

National Research Council (NRC). 2001. Nutrient Requirements of Dairy Cattle. 7th revised edn. National Academy of Science, Washington, DC.

Ospina P A, Nydam D V, Stokol T and Overton T R. 2010. Associations of elevated non-esterified fatty acids and bhydroxybutyrate concentrations with early lactation reproductive performance and milk production in transition dairy cattle in the northeastern United States. Journal of Dairy Science 93(4): 1596–1603. DOI: https://doi.org/10.3168/jds.2009-2852

Pryce J E, Coffey M P, Brotherstone S H and Woolliams J A. 2002. Genetic relationships between calving interval and body condition score conditional on milk yield. Journal of Dairy Science 85(6): 1590–95. DOI: https://doi.org/10.3168/jds.S0022-0302(02)74229-X

Sordillo L M and Raphael W. 2013. Significance of metabolic stress, lipid mobilization, and inflammation on transition cow disorders. Veterinary Clinics: Food Animal Practice 29(2): 267–78. DOI: https://doi.org/10.1016/j.cvfa.2013.03.002

Sordillo L M, Pighetti G M and Davis M R. 1995. Enhanced production of bovine tumor necrosis factor-α during the periparturient period. Veterinary Immunology and Immunopathology 49(3): 263–70. DOI: https://doi.org/10.1016/0165-2427(95)05465-0

Sundrum A. 2015. Metabolic disorders in the transition period indicate that the dairy cows ability to adapt is overstressed. Animals 5(4): 978–1020. DOI: https://doi.org/10.3390/ani5040395

Tothova C, Nagy O and Kovac G. 2014. Relationship between some variables of protein profile and indicators of lipomobilization in dairy cows after calving. Archives Animal Breeding 57(1): 1–9. DOI: https://doi.org/10.7482/0003-9438-57-019

Uhlar C M and Whitehead A S. 1999. Serum amyloid A, the major vertebrate acute phase reactant. FEBS Journal 265(2): 501– 23. DOI: https://doi.org/10.1046/j.1432-1327.1999.00657.x

Wathes D C, Cheng Z, Chowdhury W, Fenwick M A, Fitzpatrick R, Morris D G, Patton J and Murphy J J. 2009. Negative energy balance alters global gene expression and immune responses in the uterus of postpartum dairy cows. Physiological Genomics 39(1): 1–13. DOI: https://doi.org/10.1152/physiolgenomics.00064.2009

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Submitted

2018-09-26

Published

2018-09-26

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How to Cite

WANKHADE, P. R., MANIMARAN, A., KUMARESAN, A., JEYAKUMAR, S., RAMESHA, K. P., SEJIAN, V., RAJENDRAN, D., BAGATH, M., & SIVARAM, M. (2018). Metabolism and immune status during transition period influences the lactation performance in Zebu (Bos indicus) cows. The Indian Journal of Animal Sciences, 88(9), 1064-1069. https://doi.org/10.56093/ijans.v88i9.83556
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