Efficacy of beta-lactams against experimental pneumococcal endocarditis caused by strains with different

Cristina Pichardo1, Fernando Docobo-Pérez, Maria E Pachón-Ibáñez

  • 1Infectious Diseases Service, Virgen del Rocío University Hospitals, Sevilla, Spain. cristina.pichardo.exts@juntadeandalucia.es

Abstract

Insights

Penicillin remains effective against Streptococcus pneumoniae infections, even with resistant strains. This study suggests current susceptibility breakpoints for penicillin may need reevaluation.

Area of Science:

  • Microbiology and Infectious Diseases
  • Pharmacology and Therapeutics

Background:

  • Streptococcus pneumoniae is a significant cause of bacterial infections.
  • Antimicrobial resistance in S. pneumoniae necessitates ongoing evaluation of treatment efficacy.
  • Understanding the in vitro and in vivo activity of antibiotics is crucial for clinical decision-making.

Purpose of the Study:

  • To compare the in vitro and in vivo activity of penicillin, cefotaxime, and ceftriaxone against Streptococcus pneumoniae.
  • To assess antibiotic efficacy using strains with varying penicillin minimum inhibitory concentrations (MICs).

Main Methods:

  • In vitro time-kill curves were performed.
  • An experimental rabbit model of endocarditis was utilized.
  • Three S. pneumoniae strains with penicillin MICs of 0.015, 0.25, and 2 mg/L were tested.

Main Results:

  • Penicillin demonstrated significant efficacy in clearing bacteria from vegetations and blood, regardless of penicillin susceptibility (P < 0.01 vs. controls).
  • Cefotaxime and ceftriaxone exhibited similar efficacy to penicillin in the in vivo model.
  • Penicillin showed superior results in the in vivo endocarditis model compared to in vitro time-kill curves.

Conclusions:

  • Penicillin is efficacious for treating pneumococcal infections, including those caused by strains with MICs up to 2 mg/L (excluding meningitis).
  • Current breakpoints for defining S. pneumoniae susceptibility and resistance to penicillin warrant review.
  • Reevaluation of breakpoints is suggested, similar to recent changes for amoxicillin and third-generation cephalosporins.

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