Characterization of immune response in Staphylococcus aureus chronically infected bovine mammary glands during active involution

Comp Immunol Microbiol Infect Dis. 2017 Oct:54:51-60. doi: 10.1016/j.cimid.2017.08.005. Epub 2017 Sep 6.

Abstract

The aim of this study was to characterize the immune response in Staphylococcus aureus chronically infected bovine mammary glands during active involution. Twenty-one Holstein non-pregnant cows in late lactation either uninfected or with chronic naturally acquired S. aureus intramammary infections (IMI) were included in this study. Cows were slaughtered at 7, 14 and 21 d after cessation of milking and samples for immunohistochemical analysis were taken. Protein expression of toll-like receptor 2 (TLR2) and TLR4 was significantly higher in S. aureus-infected quarters than in uninfected controls at the three involution stages studied. Protein expression of tumor necrosis factor-alpha (TNF-α), interleukin (IL)-1α and IL-17 was significantly affected by IMI; being higher in S. aureus-infected than uninfected quarters during all evaluated stages. In S. aureus-infected and uninfected quarters protein expression of lactoferrin increased from day 7-14 of involution, decreasing significantly to day 21 in mammary quarters with chronic infections. The number of monocytes-macrophages was significantly higher in S. aureus-infected than in uninfected control quarters at 7 and 21 d of involution. The number of T lymphocytes was significantly higher in S. aureus-infected than in uninfected quarters at 7 and 14 d of involution while the number of B lymphocytes was significantly higher in S. aureus-infected than in uninfected quarters during all evaluated stages, showing a progressive increase as involution advanced. These results demonstrated a sustained and exacerbated innate and adaptive immune response during chronic S. aureus IMI, playing a critical role in the infection control during active involution.

Keywords: Immune response; Involution; Mastitis; Staphylococcus aureus.

MeSH terms

  • Adaptive Immunity*
  • Animals
  • Antibodies, Bacterial / immunology
  • Antibody Specificity
  • Cattle
  • Female
  • Immunity, Innate*
  • Interleukin-17 / analysis
  • Interleukin-1alpha / analysis
  • Lymphocytes / immunology
  • Macrophages / immunology
  • Mammary Glands, Animal / cytology
  • Mammary Glands, Animal / immunology*
  • Mammary Glands, Animal / microbiology
  • Mastitis, Bovine / immunology*
  • Mastitis, Bovine / microbiology
  • Staphylococcal Infections / immunology
  • Staphylococcal Infections / veterinary*
  • Staphylococcus aureus / immunology*
  • Toll-Like Receptor 2 / analysis
  • Tumor Necrosis Factor-alpha / analysis

Substances

  • Antibodies, Bacterial
  • Interleukin-17
  • Interleukin-1alpha
  • Toll-Like Receptor 2
  • Tumor Necrosis Factor-alpha