Inflammation Mediators Regulate the Microbiota Resistance to Adverse Factors

Bull Exp Biol Med. 2020 Nov;170(1):49-52. doi: 10.1007/s10517-020-05002-5. Epub 2020 Nov 22.

Abstract

We studied the effects of IL-1β, IL-8, TNFα, and prostaglandin E2α in concentrations typically observed in health and during inflammation on the growth of vaginal microbiota and its resistance to factors inhibiting the synthesis of proteins, nucleic acids, and peptidoglycans. An increase in the cytokine levels, characteristic of inflammation, inhibits the growth of Lactobacillus population and improves its resistance to adverse factors. The growth of the population of opportunistic microorganisms (S. aureus, E. coli) is stimulated under these conditions, while their resistance to adverse factors decreases. Hence, it seems that the cytokines regulate the behavior of the host cells and of its bacterial symbionts.

Keywords: cytokines; inflammation; interspecies communication; lactobacilli; resistance.

MeSH terms

  • Body Fluids / microbiology
  • Case-Control Studies
  • Dinoprostone / immunology
  • Dinoprostone / pharmacology*
  • Drug Resistance, Bacterial / drug effects
  • Escherichia coli / drug effects
  • Escherichia coli / growth & development
  • Female
  • Host-Pathogen Interactions
  • Humans
  • Inflammation
  • Inflammation Mediators / immunology
  • Inflammation Mediators / pharmacology*
  • Interleukin-1beta / immunology
  • Interleukin-1beta / pharmacology*
  • Interleukin-8 / immunology
  • Interleukin-8 / pharmacology*
  • Lactobacillus / drug effects
  • Lactobacillus / growth & development
  • Microbiota / drug effects*
  • Microbiota / immunology
  • Staphylococcus aureus / drug effects
  • Staphylococcus aureus / growth & development
  • Tumor Necrosis Factor-alpha / immunology
  • Tumor Necrosis Factor-alpha / pharmacology*
  • Vagina / immunology
  • Vagina / microbiology
  • Vaginosis, Bacterial / immunology
  • Vaginosis, Bacterial / microbiology*

Substances

  • CXCL8 protein, human
  • IL1B protein, human
  • Inflammation Mediators
  • Interleukin-1beta
  • Interleukin-8
  • Tumor Necrosis Factor-alpha
  • Dinoprostone