Biofilm formation or internalization into epithelial cells enable Streptococcus pyogenes to evade antibiotic

Taiji Ogawa1, Yutaka Terao, Hisashi Okuni

  • 1Department of Oral and Molecular Microbiology, Osaka University Graduate School of Dentistry, 1-8 Yamadaoka, Suita, Osaka 565-0871, Japan.

Microbial Pathogenesis
|March 30, 2011
PubMed

Insights

Recurrent Streptococcus pyogenes pharyngitis involves emm type-specific bacterial features enabling antibiotic resistance. Some strains evade penicillin by internalizing into cells and forming protective biofilms, requiring combination therapies for eradication.

Area of Science:

  • Microbiology
  • Infectious Diseases
  • Bacterial Pathogenesis

Background:

  • Streptococcus pyogenes is a common cause of pharyngitis, but treatment failures occur.
  • Understanding resistance mechanisms is crucial for effective pharyngitis management.

Purpose of the Study:

  • Investigate mechanisms of antibiotic resistance in recurrent Streptococcus pyogenes pharyngitis.
  • Identify emm type-specific features contributing to treatment failure.

Main Methods:

  • Bacterial isolation and serotyping (emm typing).
  • Biofilm formation assessment (fluorescence microscopy, Live/Dead staining).
  • Antimicrobial peptide susceptibility testing.
  • Epithelial cell invasion assays.
  • Flow cytometry for PrtF1 protein expression.

Main Results:

  • emm6 strains showed higher biofilm production; emm12 strains exhibited greater invasion capacity.
  • S. pyogenes survived in biofilms despite high antibiotic concentrations.
  • Bacterial internalization into epithelial cells provided temporary protection from penicillin.
  • Combined antibiotic therapies were more effective against invasive strains.
  • emm12 strains with high invasiveness expressed PrtF1 protein.

Conclusions:

  • emm type-specific bacterial traits, including biofilm formation and cellular invasion, contribute to antibiotic treatment failure in S. pyogenes pharyngitis.
  • Antimicrobial peptides show potential for biofilm inhibition.
  • Targeting invasion mechanisms and using combination therapies may improve eradication of resistant S. pyogenes strains.

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