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Molecular characterization of macrolide resistance mechanisms among Streptococcus pneumoniae and Streptococcus
D J Farrell1, I Morrissey, S Bakker
1GR Micro Ltd, 7-9 William Road, London NW1 3ER, UK. D.Farrell@grmicro.co.uk
Abstract:
In this study, the distribution of macrolide resistance mechanisms was determined for isolates of Streptococcus pneumoniae and Streptococcus pyogenes obtained from the PROTEKT 1999-2000 study (a global, longitudinal study of the antibacterial susceptibility of bacterial pathogens associated with community-acquired lower respiratory tract infections). The global macrolide resistance mechanism distribution results for 1043 macrolide-resistant S. pneumoniae isolates collected from 25 countries were as follows: 35.3% mef(A), 56.2% erm(B), 6.8% both mef(A) and erm(B), 0.2% erm(A) subclass erm(TR) and 1.5% negative for mechanisms tested. Mechanisms of macrolide resistance were found to vary widely between countries and different geographical regions with mef(A) predominating in North America and erm(B) in Europe. Approximation of genotype from macrolide MIC without molecular determination of the mechanism of resistance resulted in an error of 10.2% (106 isolates). Overall, for 143 macrolide-resistant S. pyogenes isolates, 46.1% of the isolates tested were mef(A), 30.8% were erm(B), 23.1% were erm(A) subclass erm(TR) and no isolates were negative for all the genetic markers tested. Again, the distribution varied widely between countries and geographical regions. This study provides valuable baseline data for the continued monitoring of the evolution of macrolide resistance development in these important respiratory tract pathogens. The ketolide telithromycin retained excellent anti-pneumococcal activity irrespective of macrolide resistance mechanism, having a MIC(90) of 0.25, 0.5 and 0.5 mg/L against mef(A), erm(B) and mef(A)+erm(B) macrolide-resistant S. pneumoniae, respectively. It also exhibited potent activity against S. pyogenes that had become resistant to macrolides via either mef(A), (MIC(90 )0.5 mg/L) or erm(TR), (MIC(90) 0.03 mg/L).
Insights
Macrolide resistance mechanisms in Streptococcus pneumoniae and Streptococcus pyogenes vary globally, with different genes predominating by region. Telithromycin shows potent activity against these resistant pathogens.
Area of Science:
- Microbiology
- Infectious Diseases
- Pharmacology
Background:
- Macrolide resistance in Streptococcus pneumoniae and Streptococcus pyogenes is a growing concern for community-acquired lower respiratory tract infections.
- Understanding the distribution of resistance mechanisms is crucial for effective treatment strategies.
- The PROTEKT study provided longitudinal data on antibacterial susceptibility globally.
Purpose of the Study:
- To determine the distribution of macrolide resistance mechanisms in S. pneumoniae and S. pyogenes isolates.
- To analyze geographical variations in resistance mechanisms.
- To evaluate the in vitro activity of telithromycin against macrolide-resistant strains.
Main Methods:
- Analysis of 1043 macrolide-resistant S. pneumoniae and 143 S. pyogenes isolates from the PROTEKT 1999-2000 study.
- Molecular determination of macrolide resistance mechanisms (mef(A), erm(B), erm(TR)).
- Determination of Minimum Inhibitory Concentrations (MICs) for telithromycin against resistant isolates.
Main Results:
- Globally, erm(B) (56.2%) and mef(A) (35.3%) were the most common mechanisms in S. pneumoniae; mef(A) predominated in North America, erm(B) in Europe.
- Resistance mechanisms varied significantly by country and region for both S. pneumoniae and S. pyogenes.
- Telithromycin demonstrated potent activity against macrolide-resistant S. pneumoniae and S. pyogenes, irrespective of the resistance mechanism.
Conclusions:
- Significant geographical variation exists in macrolide resistance mechanisms for key respiratory pathogens.
- This data provides a baseline for monitoring the evolution of macrolide resistance.
- Telithromycin retains excellent activity against macrolide-resistant S. pneumoniae and S. pyogenes, suggesting its potential therapeutic value.