Poor stimulation of bovine dendritic cells by Mycobacterium bovis culture supernatant and surface extract is associated with decreased activation of ERK and NF- κ B and higher expression of SOCS1 and 3

Innate Immun. 2020 Aug;26(6):537-546. doi: 10.1177/1753425920929759. Epub 2020 Jun 8.

Abstract

The cell envelope of pathogenic mycobacteria interfaces with the host. As such, the interaction of bacterial products localized at or released from the cell surface with the host's immune system can determine the fate of the bacterium in its host. In this study, the effects of three different types of Mycobacterium bovis cell envelope fractions-purified protein derivative, total cell wall lipids and culture supernatant and surface extract-on bovine dendritic cells were assessed. We found that the culture supernatant and surface extract fraction induced little to no production of the pro-inflammatory cytokines TNF-α and IL-12 in bovine dendritic cells. Moreover, this muted response was associated with poor activation of ERK and NF-κB, both of which are critical for the pro-inflammatory response. Furthermore, culture supernatant and surface extract treatment increased the expression of suppressor of cytokine signaling 1 and 3, both of which are negative regulators of pro-inflammatory signaling, in bovine dendritic cells. These observations taken together suggest the M. bovis culture supernatant and surface extract fraction contain immunomodulatory molecules that may aid in M. bovis pathogenesis.

Keywords: Bovine tuberculosis; cell wall lipid; culture supernatant and surface extract; dendritic cells; immunomodulation; innate immunity; pro-inflammatory immune response.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cattle
  • Cell Differentiation
  • Cells, Cultured
  • Culture Media, Conditioned / metabolism
  • Dendritic Cells / immunology*
  • Immunomodulation
  • Inflammation Mediators / metabolism
  • Interleukin-12 / metabolism
  • MAP Kinase Signaling System
  • Mycobacterium bovis / physiology*
  • NF-kappa B / metabolism*
  • Suppressor of Cytokine Signaling 1 Protein / genetics
  • Suppressor of Cytokine Signaling 1 Protein / metabolism*
  • Suppressor of Cytokine Signaling 3 Protein / genetics
  • Suppressor of Cytokine Signaling 3 Protein / metabolism*
  • Tuberculosis, Bovine / genetics
  • Tuberculosis, Bovine / metabolism*
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Culture Media, Conditioned
  • Inflammation Mediators
  • NF-kappa B
  • Suppressor of Cytokine Signaling 1 Protein
  • Suppressor of Cytokine Signaling 3 Protein
  • Tumor Necrosis Factor-alpha
  • Interleukin-12