Resistance of Peptostreptococcus spp. to macrolides and lincosamides: inducible and constitutive phenotypes

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M Reig1, A Moreno, F Baquero

  • 1Servicio de Microbiología, Hospital Ramón y Cajal, Instituto Nacional de la Salud, Madrid, Spain.

Insights

Erythromycin and clindamycin resistance was studied in Peptostreptococcus strains. Inducible resistance was found in 5.1% of strains, while 17.7% showed constitutive resistance to these antibiotics.

Area of Science:

  • Microbiology
  • Infectious Diseases
  • Pharmacology

Background:

  • Peptostreptococcus species are anaerobic bacteria implicated in various infections.
  • Antibiotic resistance, particularly to macrolides and lincosamides, is a growing concern in clinical settings.
  • Understanding resistance patterns is crucial for effective treatment strategies.

Purpose of the Study:

  • To investigate the antimicrobial activity of erythromycin and clindamycin against Peptostreptococcus strains.
  • To identify and characterize patterns of antibiotic resistance, including inducible and constitutive resistance phenotypes.

Main Methods:

  • Susceptibility testing of 350 Peptostreptococcus strains against erythromycin and clindamycin.
  • Determination of Minimum Inhibitory Concentrations (MICs) for both antibiotics.
  • Phenotypic characterization of inducible and constitutive macrolide-lincosamide resistance.

Main Results:

  • 5.1% of strains exhibited dissociated resistance, indicating inducible macrolide-lincosamide resistance (clindamycin MIC ≤ 1 µg/ml; erythromycin MIC > 8 µg/ml).
  • 17.7% of strains displayed a constitutive resistance phenotype, with high MICs for both erythromycin and clindamycin (MICs > 8 µg/ml).

Conclusions:

  • A significant proportion of Peptostreptococcus strains demonstrate resistance to erythromycin and clindamycin.
  • The presence of both inducible and constitutive resistance mechanisms highlights the need for careful antibiotic selection.
  • Monitoring antibiotic resistance in Peptostreptococcus is essential for guiding therapeutic choices.

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