Effect of the Ketone Body Beta-Hydroxybutyrate on the Innate Defense Capability of Primary Bovine Mammary Epithelial Cells

PLoS One. 2016 Jun 16;11(6):e0157774. doi: 10.1371/journal.pone.0157774. eCollection 2016.

Abstract

Negative energy balance and ketosis are thought to cause impaired immune function and to increase the risk of clinical mastitis in dairy cows. The present in vitro study aimed to investigate the effect of elevated levels of the predominant ketone body β-hydroxybutyrate on the innate defense capability of primary bovine mammary epithelial cells (pbMEC) challenged with the mastitis pathogen Escherichia coli (E. coli). Therefore, pbMEC of healthy dairy cows in mid- lactation were isolated from milk and challenged in culture with 3 mM BHBA and E. coli. pbMEC stimulated with E. coli for 6 h or 30 h showed an up-regulation of several innate immune genes, whereas co-stimulation of pbMEC with 3 mM BHBA and E. coli resulted in the down-regulation of CCL2, SAA3, LF and C3 gene expression compared to the challenge with solely the bacterial stimulus. These results indicated that increased BHBA concentrations may be partially responsible for the higher mastitis susceptibility of dairy cows in early lactation. Elevated levels of BHBA in blood and milk during negative energy balance and ketosis are likely to impair innate immune function in the bovine mammary gland by attenuating the expression of a broad range of innate immune genes.

MeSH terms

  • 3-Hydroxybutyric Acid / pharmacology*
  • Animals
  • Cattle
  • Chemokine CCL2 / genetics
  • Chemokine CCL2 / immunology
  • Complement C3 / genetics*
  • Complement C3 / metabolism
  • Energy Metabolism / drug effects
  • Energy Metabolism / immunology
  • Epithelial Cells / drug effects
  • Epithelial Cells / immunology*
  • Epithelial Cells / microbiology
  • Escherichia coli / growth & development*
  • Female
  • Gene Expression Profiling
  • Gene Expression Regulation
  • Immunity, Innate*
  • Lactoferrin / genetics
  • Lactoferrin / immunology
  • Mammary Glands, Animal / immunology
  • Mammary Glands, Animal / microbiology
  • Serum Amyloid A Protein / genetics
  • Serum Amyloid A Protein / immunology
  • Signal Transduction
  • Toll-Like Receptors / genetics*
  • Toll-Like Receptors / immunology

Substances

  • Chemokine CCL2
  • Complement C3
  • Serum Amyloid A Protein
  • Toll-Like Receptors
  • Lactoferrin
  • 3-Hydroxybutyric Acid

Grants and funding

This work was supported by the German Research Foundation (DFG) and the Technische Universität München within the funding program Open Access Publishing. Furthermore, this study was funded by the “Vereinigung zur Förderung der Milchwissenschaftlichen Forschung an der Technischen Universität München e. V.” (Freising, Germany). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.