Differential adaptation of metabolic inflammation between primiparous and multiparous Zebu cows during transition period


Abstract views: 107 / PDF downloads: 121

Authors

https://doi.org/10.56093/ijans.v92i7.118208

Keywords:

Deoni cows, Inflammatory indicators, Metabolic indicators, Milk yield, Parity, Transition period.

Abstract

This study aimed to estimate the changes in the milk yield, milk fat, energy indicators [NEFA, BHBA, Dry Matter
Intake (DMI) and Body Condition Score (BCS)] and concentration of innate immune molecules (Haptoglobin: Hp,
Serum Amyloid A: SAA, TLR-4, TNF-α, IL-1β, IL-6, and IL-8), during the transition period in primiparous and
multiparous dual-purpose zebu (Deoni) cows. The blood sample was collected at weekly intervals during pre-partum (-21±2, -14±1, -7±1, d), date of calving (day 0), and postpartum period (3±1, 7±1, 14±1, 21±2 d) for estimation
of the above plasma variables using commercially available bovine specific ELISA kits. DMI and BCS during
the corresponding period were also recorded. Data were analyzed using a linear mixed model considering group,
time and their interaction as fixed effects. Group, time and their interaction had significant effect on DMI where
primiparous cows consumed higher DMI during early postpartum period as compared to multiparous cows. Group
alone had significant effect on milk yield, milk fat per cent and BHBA level while time alone influenced BCS.
The interaction of group and time had significant effects on plasma TLR-4 and IL-8 concentration. Group also
had significant effect on Hp and TNF-α levels. It was concluded that parity had significant effect on metabolic
and immune indicators where higher DMI during transition period resulted in more milk yield in primiparous than
multiparous indigenous (Deoni) cows.

Downloads

Download data is not yet available.

Author Biography

  • Manimaran Ayyasamy, Livestock Research Center, Southern Regional Station, ICAR-NDRI, Bengaluru, Karnataka, India
    Senior Scientist, LRC, SRS, ICAR-NDRI, Adugodi, Bengaluru 

References

Aeberhard K, Bruckmaier R M and Blum J W. 2001. Metabolic, enzymatic and endocrine status in high-yielding dairy cowspart 2. Journal of Veterinary Medicine Series A 48(2): 111– 27. DOI: https://doi.org/10.1046/j.1439-0442.2001.00294.x

Barca J, Schukken Y H and Meikle A. 2021. Increase in white blood cell counts by pegbovigrastim in primiparous and

multiparous grazing dairy cows and the interaction with prepartum body condition score and non-esterified fatty acids concentration. PLoS One 16(1): 0245149. Bionaz M, Trevisi E, Calamari L, 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.

Boro P, Kumaresan A, Pathak R, Patbandha T K, Kumari S, Yadav A, Manimaran A, Baithalu R K, Attupuram N M and Mohanty T K. 2015. Alteration in peripheral blood concentration of certain pro-inflammatory cytokines in cows developing retention of fetal membranes. Animal Reproduction Science 157: 11–16.

Bradford B J, Yuan K, Farney J K, Mamedova L K and Carpenter A J. 2015. Invited review: Inflammation during the transition to lactation: New adventures with an old flame. Journal of Dairy Science 98(10): 6631–50. DOI: https://doi.org/10.3168/jds.2015-9683

Bronzo V, Lopreiato V, Riva F, Amadori M, Curone G, Addis M F, Cremonesi P, Moroni P, Trevisi E and Castiglioni B. 2020. The role of innate immune response and microbiome in resilience of dairy cattle to disease: The mastitis model. Animals 10(8): 1397. DOI: https://doi.org/10.3390/ani10081397

Budikhina A S, Murugina N E, Maximchik P V, Dagil Y A, Nikolaeva A M, Balyasova L S, Murugin V V, Selezneva E

M, Pashchenkova Y G, Chkadua G Z and Pinegin B V. 2021. Interplay between NOD1 and TLR4 receptors in macrophages: non-synergistic activation of signaling pathways results in synergistic induction of proinflammatory gene expression. The Journal of Immunology 206(9): 2206–20. DOI: https://doi.org/10.4049/jimmunol.2000692

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. The Indian Journal of Animal Sciences 81(11): 1186–88.

Dervishi E, Zhang G, Hailemariam D, Goldansaz S A, Deng Q, Dunn S M and Ametaj B N. 2016. Alterations

in innate immunity reactants and carbohydrate and lipid metabolism precede occurrence of metritis in transition dairy cows. Research in Veterinary Science 104: 30–39.

Eckersall P D and Bell R. 2010. Acute phase proteins: Biomarkers of infection and inflammation in veterinary medicine. The Veterinary Journal 185(1): 23–27. DOI: https://doi.org/10.1016/j.tvjl.2010.04.009

Grummer R R. 1995. Impact of changes in organic nutrient metabolism on feeding the transition dairy cow. Journal of Animal Science 73(9): 2820–33. DOI: https://doi.org/10.2527/1995.7392820x

Herdt T H. 2000. Ruminant adaptation to negative energy balance: influences on the etiology of ketosis and fatty liver. Veterinary Clinics: Food Animal Practice 16(2): 215–30.

Jilek F, Pytloun P, Kubesova M, Stipkova M, Bouska 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):

–67.

Kellogg W. 2010. Body condition scoring with dairy cattle. university of Arkansas, united states department of agriculture and county governments cooperating [Online]. Available at https:// www.uaex.edu/publications/pdf/FSA-4008.pdf. Accessed on 20 November 2021. Kerhli M E. 2015. Immunological dysfunction in periparturient cows: Evidence, causes and ramifications. Proceeding of Florida Ruminant Nutrition Symposium 14–29. Kimura K, Reinhardt T A and Goff J P. 2006. Parturition and hypocalcemia blunts calcium signals in immune cells of dairy

cattle. Journal of Dairy Science 89(7): 2588–95.

Kuhla B. 2020. Pro-inflammatory cytokines and hypothalamic inflammation: Implications for insufficient feed intake of transition dairy cows. Animal 14(1): 65–77. DOI: https://doi.org/10.1017/S1751731119003124

Kumari S, Prasad S, Patbandha T K, Pathak R, Kumaresan A, Boro P, Manimaran A and Mohanty T K. 2016. Metabolic indicators for retention of fetal membranes in Zebu and crossbred dairy cattle. Animal Production Science 56(7): 1113–20. DOI: https://doi.org/10.1071/AN14941

Kuralkar S V, Bankar P S, Chopade M M, Kuralkar P and Dhaware S A. 2014. Phenotypic characteristics, production

and reproduction performance of Deoni cattle in its native tract. The Indian Journal of Animal Sciences 84(1): 75–77.

LeBlanc S. 2010. Monitoring metabolic health of dairy cattle in the transition period. Journal of Reproduction and Development 56: 29–35.

Manimaran A, Kumaresan A, Jeyakumar S, Mohanty T K, Sejian V, Kumar N, Sreela L, Prakash M A, Mooventhan P,

Anantharaj A and Das D N. 2016. Potential of acute phase proteins as predictor of postpartum uterine infections during transition period and its regulatory mechanism in dairy cattle. Veterinary World 9(1): 91–100. DOI: https://doi.org/10.14202/vetworld.2016.91-100

Manimaran A, Wankhade P R, Kumaresan A, Patbandha T K, Sivaram M, Jeyakumar S and Rajendran D. 2021. Peripheral blood concentration of toll-like receptor-4 and its accuracy for prediction of postpartum performances of transition Zebu (Bos indicus) cows. The Indian Journal of Animal Sciences 91(8): 628–31.

Miller N, Delbecchi L, Petitclerc D, Wagner G F, Talbot B G and Lacasse P. 2006. Effect of stage of lactation and parity

on mammary gland cell renewal. Journal of Dairy Science 89(12): 4669–77.

National Research Council (NRC). 2001. Nutrient Requirements of Dairy Cattle. 7th revised edition. National Academies Press, Washington, DC. Neave H W, Lomb J, Von Keyserlingk M A G, BehnamShabahang A and Weary D M. 2017. Parity differences in the behavior of transition dairy cows. Journal of Dairy Science 100(1): 548–61.

Ohtsuka H, Terasawa S, Watanabe C, Kohiruimaki M, Mukai M, Ando T, Petrovski K R and Morris S. 2010. Effect of parity on lymphocytes in peripheral blood and colostrum of healthy Holstein dairy cows. Canadian Journal of Veterinary Research 74(2): 130–35.

Ospina P A, Nydam D V, Stokol T and Overton T R. 2010. Associations of elevated non-esterified fatty acids and

β-hydroxybutyrate 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.

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

Reshalaitihan M, Wynn S, Teramura M, Sato T and Hanada M. 2020. Effect of parity number on the dry matter intake of dairy cows during the first week after calving. Animal Science Journal 91(1): 13314. DOI: https://doi.org/10.1111/asj.13314

Roche J R, Friggens N C, Kay J K, Fisher M W, Stafford K J and Berry D P. 2009. Invited review: Body condition score

and its association with dairy cow productivity, health, and welfare. Journal of Dairy Science 92(12): 5769–5801.

Ruprechter G, de Lourdes Adrien M, Larriestra A, Meotti O, Batista C, Meikle A and Noro M. 2018. Metabolic predictors of peri-partum diseases and their association with parity in dairy cows. Research in Veterinary Science 118: 191–98.

Seifi H A, LeBlanc S J, Leslie K E and Duffield T F. 2011. Metabolic predictors of post-partum disease and culling risk

in dairy cattle. The Veterinary Journal 188(2): 216–20.

Sharma D. 2021. ῾Prevalence of health disorders in cows with special reference to subclinical mastitis under organized and unorganized production conditions.᾿ Ph.D. thesis, ICARNational Dairy Research Institute, Karnal, Haryana, India.

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

Soumya N P, Das D N, Jeyakumar S, Mondal S, Mor A and Mundhe U T. 2017. Differential expression of ISG 15

mRNA in peripheral blood mononuclear cells of nulliparous and multiparous pregnant versus non-pregnant Bos indicus cattle. Reproduction in Domestic Animals 52(1): 97–106.

Theurer M L, McGuire M A and Higgins J J. 2003. Relationships between body condition score and peak milk. Journal of Dairy Science 86(1): 282.

Trevisi E, Moscati L and Amadori M. 2016. Disease-predicting and prognostic potential of innate immune responses to noninfectious stressors: Human and animal models, Elseviers Inc. The Innate Immune Response to Noninfectious Stressors pp. 209–35. Wang Y, Huo P, Sun Y and Zhang Y. 2019. Effects of body condition score changes during peripartum on the postpartum health and production performance of primiparous dairy cows. Animals 9(12): 1159. DOI: https://doi.org/10.3390/ani9121159

Wankhade P R, Manimaran A, Kumaresan A, Jeyakumar S, Ramesha K P, Sejian V, Rajendran D, Bagath M and 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): 1064–69.

Wankhade P R, Manimaran A, Kumaresan A, Jeyakumar S, Ramesha K P, Sejian V, Rajendran D and Varghese M R. 2017. Metabolic and immunological changes in transition dairy cows: A review. Veterinary World 10(11): 1367–77. DOI: https://doi.org/10.14202/vetworld.2017.1367-1377

Wankhade P R, Manimaran A, Kumaresan A, Jeyakumar S, Sejian V, Rajendran D, Bagath M, Sivaram M, Ramesha K

P and Varghese M R. 2019. Active immune system and dry matter intake during the transition period are associated with postpartum fertility in lactating Zebu cows. Livestock Science 228: 18–24.

Watanabe A, Yagi Y, Shiono H, Yokomizo Y and Inumaru S. 2008. Effects of intramammary infusions of interleukin-8 on milk protein composition and induction of acute-phase protein in cows during mammary involution. Canadian Journal of Veterinary Research 72(3): 291–96.

Wathes D C, Cheng Z, Bourne N, Taylor V J, Coffey M P and Brotherstone S. 2007. Differences between primiparous and multiparous dairy cows in the inter-relationships between metabolic traits, milk yield and body condition score in the periparturient period. Domestic Animal Endocrinology 33(2): 203–25. DOI: https://doi.org/10.1016/j.domaniend.2006.05.004

Zarei S, Ghorbani G R, Khorvash M, Martin O, Mahdavi A H and Riasi A. 2017. The impact of season, parity, and volume of colostrum on Holstein dairy cows colostrum composition. Agricultural Sciences 8: 572–81.

Zebeli Q, Ghareeb K, Humer E, Metzler-Zebeli B U and Besenfelder U. 2015. Nutrition, rumen health and inflammation in the transition period and their role on overall health and fertility in dairy cows. Research in Veterinary Science 103: 126–36.

Zhang G, Hailemariam D, Dervishi E, Goldansaz S A, Deng Q, Dunn S M and Ametaj B N. 2016. Dairy cows affected

by ketosis show alterations in innate immunity and lipid and carbohydrate metabolism during the dry off period and

postpartum. Research in Veterinary Science 107: 246–56.

Downloads

Submitted

2021-11-23

Published

2022-06-19

Issue

Section

Articles

How to Cite

WANKHADE, P. R., Ayyasamy, M., KUMARESAN, A., SIVARAM, M., SEJIAN, V., & RAJENDRAN, D. (2022). Differential adaptation of metabolic inflammation between primiparous and multiparous Zebu cows during transition period. The Indian Journal of Animal Sciences, 92(7), 830-836. https://doi.org/10.56093/ijans.v92i7.118208
Citation