Probiotic Exopolysaccharide Protects against Systemic Staphylococcus aureus Infection, Inducing Dual-Functioning

Wonbeom Paik1, Francis Alonzo1, Katherine L Knight2

  • 1Department of Microbiology and Immunology, Loyola University Chicago, Maywood, Illinois, USA.

Infection and Immunity
|November 7, 2018
PubMed

Insights

Bacillus subtilis exopolysaccharide (EPS) protects mice against Staphylococcus aureus infection by creating unique macrophages. These hybrid immune cells reduce inflammation and bacterial load, improving survival rates.

Area of Science:

  • Immunology
  • Microbiology
  • Biochemistry

Background:

  • Staphylococcus aureus infections lead to high mortality.
  • Exopolysaccharide (EPS) from Bacillus subtilis induces anti-inflammatory M2 macrophages.
  • EPS has previously shown protective effects against Citrobacter rodentium-induced colitis.

Purpose of the Study:

  • To determine if Bacillus subtilis EPS can protect against systemic Staphylococcus aureus infection.
  • To investigate the immunomodulatory effects of EPS on macrophages and host response.

Main Methods:

  • Mice were treated with EPS and subsequently infected with Staphylococcus aureus.
  • Survival rates, weight loss, systemic inflammation, and bacterial burden were assessed.
  • Macrophage phenotypes, intracellular bacterial growth restriction via reactive oxygen species (ROS), T cell activation, and systemic cytokine induction were analyzed.

Main Results:

  • EPS treatment significantly enhanced survival and reduced weight loss, inflammation, and bacterial burden in mice infected with S. aureus.
  • EPS-induced macrophages exhibited an M2 phenotype but also restricted intracellular S. aureus growth via ROS.
  • EPS-induced macrophages limited T cell activation by S. aureus superantigens and abrogated systemic interferon-gamma induction.

Conclusions:

  • Bacillus subtilis EPS acts as an immunomodulatory agent.
  • EPS induces hybrid macrophages with dual functions: enhancing antibacterial immunity and limiting inflammation.
  • This dual action reduces disease severity and promotes host survival during S. aureus infection.

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