The absence of microbiota delays the inflammatory response to Cryptococcus gattii

Int J Med Microbiol. 2016 Jun;306(4):187-95. doi: 10.1016/j.ijmm.2016.03.010. Epub 2016 Apr 6.

Abstract

The inflammatory response plays a crucial role in infectious diseases, and the intestinal microbiota is linked to maturation of the immune system. However, the association between microbiota and the response against fungal infections has not been elucidated. Our aim was to evaluate the influence of microbiota on Cryptococcus gattii infection. Germ-free (GF), conventional (CV), conventionalized (CVN-mice that received feces from conventional animals), and LPS-stimulated mice were infected with C. gattii. GF mice were more susceptible to infection, showing lower survival, higher fungal burden in the lungs and brain, increased behavioral changes, reduced levels of IFN-γ, IL-1β and IL-17, and lower NFκBp65 phosphorylation compared to CV mice. Low expression of inflammatory cytokines was associated with smaller yeast cells and polysaccharide capsules (the main virulence factor of C. gattii) in the lungs, and less tissue damage. Furthermore, macrophages from GF mice showed reduced ability to engulf, produce ROS, and kill C. gattii. Restoration of microbiota (CVN mice) or LPS administration made GF mice more responsive to infection, which was associated with increased survival and higher levels of inflammatory mediators. This study is the first to demonstrate the influence of microbiota in the host response against C. gattii.

Keywords: Cryptococcosis; Cryptococcus gattii; Germ-free mice; Microbiota.

MeSH terms

  • Animals
  • Apoptosis Regulatory Proteins
  • Brain / microbiology
  • Brain / pathology
  • Colony Count, Microbial
  • Cryptococcosis / immunology*
  • Cryptococcosis / pathology*
  • Cryptococcus gattii / immunology*
  • Cytokines / metabolism
  • Disease Models, Animal
  • Disease Susceptibility*
  • Gastrointestinal Microbiome / immunology*
  • Germ-Free Life
  • Inflammation / pathology*
  • Lung / microbiology
  • Lung / pathology
  • Macrophages / immunology
  • Mice
  • Phagocytosis
  • Receptors, Immunologic
  • Receptors, Scavenger
  • Survival Analysis
  • Wiskott-Aldrich Syndrome Protein

Substances

  • Apoptosis Regulatory Proteins
  • Cd5l protein, mouse
  • Cytokines
  • Receptors, Immunologic
  • Receptors, Scavenger
  • Was protein, mouse
  • Wiskott-Aldrich Syndrome Protein