Group A streptococcal myonecrosis: increased vimentin expression after skeletal-muscle injury mediates the binding of Streptococcus pyogenes

J Infect Dis. 2006 Jun 15;193(12):1685-92. doi: 10.1086/504261. Epub 2006 May 10.

Abstract

Necrotizing fasciitis and myonecrosis caused by invasive infection with group A streptococci (GAS) are life-threatening conditions that have reemerged worldwide. Half of all GAS myonecrosis cases have no known portal of entry; yet, for unknown reasons, infection becomes established precisely at the site of a prior, nonpenetrating minor injury, such as a muscle strain. We hypothesized that GAS establishes infection by binding to surface molecules that are up-regulated on injured skeletal-muscle cells. Here, we isolated and identified vimentin as the major skeletal-muscle GAS-binding protein. Furthermore, we found that vimentin expression was up-regulated on injured skeletal-muscle cells in vitro and was expressed in muscle tissues from a patient with GAS myonecrosis who died of streptococcal toxic shock syndrome. These findings provide a molecular mechanism to explain the development of severe GAS soft-tissue infections at the sites of prior minor muscle trauma. This understanding may provide a basis for novel preventive strategies or therapies for patients with this devastating infection.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Bacterial Adhesion*
  • Female
  • Humans
  • Immunohistochemistry
  • Male
  • Mass Spectrometry
  • Middle Aged
  • Molecular Sequence Data
  • Muscle, Skeletal / metabolism
  • Muscle, Skeletal / microbiology*
  • Muscle, Skeletal / pathology*
  • Necrosis
  • Streptococcal Infections / metabolism*
  • Streptococcal Infections / microbiology
  • Streptococcus pyogenes / physiology*
  • Vimentin / biosynthesis
  • Vimentin / chemistry
  • Vimentin / isolation & purification
  • Vimentin / metabolism*

Substances

  • Vimentin