Wall teichoic acids mediate increased virulence in Staphylococcus aureus

Stefanie Wanner1, Jessica Schade1, Daniela Keinhörster1

  • 1Department of Medicine, Interfacultary Institute for Microbiology and Infection Medicine (IMIT), University of Tübingen, Elfriede-Aulhorn Straße 6, 72076 Tübingen, Germany.

Nature Microbiology
|January 24, 2017
PubMed

Insights

Community-associated methicillin-resistant Staphylococcus aureus (CA-MRSA) cause skin infections. Higher amounts of wall teichoic acid (WTA) in CA-MRSA increase virulence through a T-cell mechanism, aiding abscess formation.

Area of Science:

  • Microbiology
  • Immunology
  • Infectious Diseases

Background:

  • Community-associated methicillin-resistant Staphylococcus aureus (CA-MRSA) drives a pandemic of skin and soft tissue infections.
  • The precise mechanisms behind CA-MRSA's heightened virulence remain incompletely understood.
  • Staphylococcus aureus possesses a significant cell wall component known as wall teichoic acid (WTA).

Purpose of the Study:

  • To elucidate the role of wall teichoic acid (WTA) in the pathogenesis of CA-MRSA infections.
  • To investigate the link between WTA content and the virulence of CA-MRSA strains.
  • To explore the T-cell-mediated mechanisms underlying CA-MRSA-induced abscess formation.

Main Methods:

  • Utilized an animal model to assess skin abscess induction.
  • Quantified cell-wall-associated WTA content in various S. aureus strains.
  • Analyzed the correlation between WTA levels and abscess formation, including T-cell involvement.

Main Results:

  • A positive correlation was observed between the amount of WTA and the severity of skin abscess induction.
  • CA-MRSA strains with higher WTA content (WTAhigh) demonstrated increased abscess-forming activity compared to WTAlow strains.
  • The abscess formation was dependent on WTA and involved a T-cell-mediated pathway.

Conclusions:

  • Wall teichoic acid (WTA) is a direct contributor to the strain-specific virulence of Staphylococcus aureus.
  • The findings reveal a novel WTA-dependent, T-cell-mediated mechanism driving CA-MRSA virulence.
  • This research provides insights that could inform the development of new anti-infective strategies against CA-MRSA.

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