Peripheral concentrations of metabolic and inflammatory indicators during transition period and their relationship with postpartum clinical endometritis in dairy cattle


Abstract views: 129 / PDF downloads: 126

Authors

  • AYYASAMY MANIMARAN Scientist, Southern Regional Station (SRS), Livestock Research Centre (LRC), ICAR-National Dairy Research Institute (NDRI), Adugodi, Bengaluru
  • ARUMUGAM KUMARESAN Principal Scientist, LRC, SRS, ICAR-NDRI, Karnal, Haryana.
  • S N SARKAR Principal Scientist, Division of Pharmacology, ICAR-Indian Veterinary Research Institute, Izatnagar
  • ASHA YADAV Research Scholar, ICAR-National Dairy Research Institute, Karnal, Haryana 132 001 India
  • SANJANNA BOYA Research Scholar, ICAR-National Dairy Research Institute, Karnal, Haryana 132 001 India
  • SREELA L Research Scholar, ICAR-National Dairy Research Institute, Karnal, Haryana 132 001 India
  • S S LAYEK Research Scholar, ICAR-National Dairy Research Institute, Karnal, Haryana 132 001 India
  • A K MOHANTY Principal Scientist, ICAR-National Dairy Research Institute, Karnal, Haryana 132 001 India
  • P MOOVENTHAN Scientist, ICAR-National Institute of Biotic Stress Management, Baronda, Raipur
  • PRATIK R WANKHADE ICAR-National Institute of Biotic Stress Management, Baronda, Raipur

https://doi.org/10.56093/ijans.v89i11.95861

Keywords:

Acute phase proteins, Clinical endometritis, Endometritis, Energy indicators, Pro-inflammatory cytokines, Transition period

Abstract

The aim of this study was to investigate the peripheral concentration of metabolic and inflammatory indicators during transition period and their relationship in cows that developed clinical endometritis (CE) and remained nonendometritis during later postpartum period. A total of 70 cows were selected and blood was collected from 21 days before calving to 21 days after calving. After adjusting the sampling date based on the actual calving date (–21±2, –7±1, 0, 7±1, 14±1 and 21±2 days) and health status, a minimum of 8 samples each from the CE and nonendometritis cows were used at each time point of transition period for the estimation of acute phase proteins (APPs) (haptoglobin, Hp; serum amyloid A, SAA; and alpha-1 acid glycoprotein, AGP), pro-inflammatory cytokines (IL-1ô€…, TNF-ô€„, IL-6 and IL-8) and energy indicators (NEFA, BHBA, Leptin and IGF-I) using bovine specific ELISA kits. APPs (Hp, SAA and AGP), cytokines (IL-1ô€…, TNF-ô€„, IL-6) and energy indicators (NEFA, BHBA, Leptin) levels significantly increased, while IL-8 and IGF-I levels significantly decreased in transition cows that eventually developed to CE compared to the cows which remained non-endometritis during 22–47 days postpartum. It is concluded that cows that diagnosed as CE during postpartum period were experienced negative energy balance and compromised their immune status during transition period.

Downloads

Download data is not yet available.

References

Cairoli F, Battocchio M, Veronesi M C, Brambilla D, Conserva F, Eberini I, Wait R and Gianazza E. 2006. Serum protein pattern during cow pregnancy: acute-phase proteins increase in the peri-partum period. Electrophoresis 27 1617–25 DOI: https://doi.org/10.1002/elps.200500742

Carter J N, Meredith G L, Montelongo M, Gill D R, Krehbiel C R, Payton M E and Confer A W. 2002. Relationship of vitamin E supplementation and antimicrobial treatment with acute- phase protein responses in cattle affected by naturally acquired respiratory tract disease. American Journal of Veterinary Research 63 1111–17 DOI: https://doi.org/10.2460/ajvr.2002.63.1111

Chan J P W, Chang C C, Chin C, Hsu W L, Liu W B and Chen T H. 2010. Association of increased serum acute-phase protein concentrations with reproductive performance in dairy cows with postpartum metritis. Veterinary Clinical Pathology 39(1) 72–78 DOI: https://doi.org/10.1111/j.1939-165X.2009.00182.x

Chapwanya A, Meade K G, Doherty M L, Callanan J J, Mee J F and O’Farrelly C. 2009. Histopathological and molecular evaluation of Holstein-Friesian cows postpartum: toward an improved understanding of uterine innate immunity. Theriogenology 71(9): 1396–1407. DOI: https://doi.org/10.1016/j.theriogenology.2009.01.006

Drackley J K. 1999. Biology of dairy cows during the transition period: The final frontier. Journal of Dairy Science 82 2259–73. DOI: https://doi.org/10.3168/jds.S0022-0302(99)75474-3

Dubuc J, Duffield T F, Leslie K E, Walton J S and LeBlanc S J. 2010. Risk factors for postpartum uterine diseases in dairy cows. Journal of Dairy Science 93(12): 5764–71. DOI: https://doi.org/10.3168/jds.2010-3429

Dubuc J. 2011. Postpartum uterine diseases: prevalence, impacts, and treatments. Western Canadian dairy seminar proceeding, advances in dairy technology 23: 255–67.

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

Galvao K N, Flaminio M J B F, Brittin S B, Sper R, Fraga M, Caixeta L, Ricci A, Guard C L, Butler W R and Gilbert R O. 2010. Association between uterine disease and indicators of neutrophil and systemic energy status in lactating Holstein Journal of Dairy Science 93 2926–37 DOI: https://doi.org/10.3168/jds.2009-2551

Galvao K N, Santos N R, Galvao J S and Gilbert R O. 2011. Association between endometritis and endometrial cytokine expression in postpartum Holstein cows. Theriogenology 76 290–99 DOI: https://doi.org/10.1016/j.theriogenology.2011.02.006

Giuliodori M J, Magnasco R P, Becu-Villalobos D, Lacau- Mengido I M, Risco C A and De la Sota R L. 2013. CE in an Argentinean herd of dairy cows: risk factors and reproductive efficiency. Journal of Dairy Science 96(1): 210–18. DOI: https://doi.org/10.3168/jds.2012-5682

Hammon D S, Evjen I M, Dhiman T R, Goff J P and Walters J L. 2006. Neutrophil function and energy status in Holstein cows with uterine health disorders. Veterinary Immunology and Immunopathology 113: 21–29 DOI: https://doi.org/10.1016/j.vetimm.2006.03.022

Horadagoda A, Eckersall P D, Hodgson J C, Gibbs H A and Moon G M. 1994. Immediate responses in serum TNF and acute phase protein concentrations to infection with Pasteurella haemolytica A1 in calves. Research in Veterinary Science 57(1): 129–32. DOI: https://doi.org/10.1016/0034-5288(94)90094-9

Huzzey J M, Duffield T F, LeBlanc S J, Veira D M, Weary D M and Von Keyserlingk M A G. 2009. Short communication: Haptoglobin as an early indicator of metritis. Journal of Dairy Science 92(2): 621–25. DOI: https://doi.org/10.3168/jds.2008-1526

Huzzey J M, Nydam D V, Grant R J and Overton T R. 2011. Associations of prepartum plasma cortisol, haptoglobin, fecal cortisol metabolites, and nonesterified fatty acids with postpartum health status in Holstein dairy cows. Journal of Dairy Science 94(12): 5878–89. DOI: https://doi.org/10.3168/jds.2010-3391

Jacobi S K, Gabler N K, Ajuwon K M, Davis J E and Spurlock M E. 2006. Adopicytes, myofibres and cytokine biology: new horizons in the regulation of growth and body composition. Journal of Animal Science 85 140–49 DOI: https://doi.org/10.2527/2006.8413_supplE140x

Kasimanickam R K, Kasimanickam V R, Olsen J R, Jeffress E J, Moore D A and Kastelic J P. 2013. Associations among serum pro-and anti-inflammatory cytokines, metabolic mediators, body condition, and uterine disease in postpartum dairy Reproductive Biology and Endocrinology 11(1): 103. DOI: https://doi.org/10.1186/1477-7827-11-103

Kim I H, Na K J and Yang M P. 2005. Immune responses during the peripartum period in dairy cows with postpartum endometritis. Journal of Reproduction and Development 51(6): 757–64 DOI: https://doi.org/10.1262/jrd.17036

LeBlanc S J. 2012. Interactions of metabolism, inflammation, and reproductive tract health in the postpartum period in dairy cattle. Reproduction in Domestic Animals 47 18–30 DOI: https://doi.org/10.1111/j.1439-0531.2012.02109.x

Mateus L, Costa L L D, Bernardo F and Silva J R. 2002. Influence of puerperal uterine infection on uterine involution and postpartum ovarian activity in dairy cows. Reproduction in Domestic Animals 37(1): 31–35. DOI: https://doi.org/10.1046/j.1439-0531.2002.00317.x

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

Nightingale C R, Sellers M D and Ballou M A. 2015. Elevated plasma haptoglobin concentrations following parturition are associated with elevated leukocyte responses and decreased subsequent reproductive efficiency in multiparous Holstein dairy cows. Veterinary Immunology and Immunopathology 164(1–2): 16–23. DOI: https://doi.org/10.1016/j.vetimm.2014.12.016

Overton T R and Waldron M R. 2004. Nutritional management of transition dairy cows: Strategies to optimize metabolic health. Journal of Dairy Science 87 105–19 DOI: https://doi.org/10.3168/jds.S0022-0302(04)70066-1

Petersen H H, Nielsen J P and Heegaard P M H. 2004. Application of acute phase protein measurement in veterinary clinical chemistry. Veterinary Research 35 163–87 DOI: https://doi.org/10.1051/vetres:2004002

Schoenberg K M, Perfield K L J K, Bradford B J, Boisclair Y R and Overton T R. 2011 Effects of prepartum 2,4- thiazolidinedione on insulin sensitivity, plasma concentrations of tumor necrosis factor- and leptin, and adipose tissue gene expression. Journal of Dairy Science 94 5523–32 DOI: https://doi.org/10.3168/jds.2011-4501

Sheldon I M and Dobson H. 2004. Postpartum uterine health in cattle. Animal Reproduction Science 82–83: 295–306 DOI: https://doi.org/10.1016/j.anireprosci.2004.04.006

Sheldon I M, Lewis G S, LeBlanc S and Gilbert R O. 2006. Defining postpartum uterine disease in cattle. Theriogenology 65(8): 1516–30. DOI: https://doi.org/10.1016/j.theriogenology.2005.08.021

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

Williams E J, Fischer D P, Noakes D E, England G C, Rycroft A, Dobson H and Sheldon I M. 2007. The relationship between uterine pathogen growth density and ovarian function in the postpartum dairy cow. Theriogenology 68(4): 549–59. DOI: https://doi.org/10.1016/j.theriogenology.2007.04.056

Zulu V C, Nakao T and Sawamukai Y. 2002. Insulin-like growth factor-I as a possible hormonal mediator of nutritional regulation of reproduction in cattle. Journal of Veterinary Medical Science 64(8): 657–65. DOI: https://doi.org/10.1292/jvms.64.657

Downloads

Submitted

2019-12-04

Published

2019-12-04

Issue

Section

Articles

How to Cite

MANIMARAN, A., KUMARESAN, A., SARKAR, S. N., YADAV, A., BOYA, S., L, S., LAYEK, S. S., MOHANTY, A. K., MOOVENTHAN, P., & WANKHADE, P. R. (2019). Peripheral concentrations of metabolic and inflammatory indicators during transition period and their relationship with postpartum clinical endometritis in dairy cattle. The Indian Journal of Animal Sciences, 89(11), 1205–1210. https://doi.org/10.56093/ijans.v89i11.95861
Citation