Staphylococcus aureus vs. Osteoblast: Relationship and Consequences in Osteomyelitis

Front Cell Infect Microbiol. 2015 Nov 26:5:85. doi: 10.3389/fcimb.2015.00085. eCollection 2015.

Abstract

Bone cells, namely osteoblasts and osteoclasts work in concert and are responsible for bone extracellular matrix formation and resorption. This homeostasis is, in part, altered during infections by Staphylococcus aureus through the induction of various responses from the osteoblasts. This includes the over-production of chemokines, cytokines and growth factors, thus suggesting a role for these cells in both innate and adaptive immunity. S. aureus decreases the activity and viability of osteoblasts, by induction of apoptosis-dependent and independent mechanisms. The tight relationship between osteoclasts and osteoblasts is also modulated by S. aureus infection. The present review provides a survey of the relevant literature discussing the important aspects of S. aureus and osteoblast interaction as well as the ability for antimicrobial peptides to kill intra-osteoblastic S. aureus, hence emphasizing the necessity for new anti-infectious therapeutics.

Keywords: Staphylococcus aureus; antibiotics; antimicrobial peptide; inflammation; internalization; osteoblast; phenol soluble modulin; small colony variants.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Antimicrobial Cationic Peptides / metabolism
  • Apoptosis
  • Cell Survival
  • Host-Pathogen Interactions*
  • Humans
  • Immunity, Innate
  • Microbial Viability / drug effects
  • Osteoblasts / immunology
  • Osteoblasts / microbiology*
  • Osteoblasts / physiology
  • Osteoclasts / microbiology
  • Osteoclasts / physiology
  • Osteomyelitis / microbiology*
  • Osteomyelitis / pathology*
  • Staphylococcal Infections / microbiology*
  • Staphylococcal Infections / pathology*
  • Staphylococcus aureus / drug effects
  • Staphylococcus aureus / immunology
  • Staphylococcus aureus / physiology*

Substances

  • Antimicrobial Cationic Peptides