JAC Advance Access originally published online on June 23, 2004
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Journal of Antimicrobial Chemotherapy 2004 54(2):542-545; doi:10.1093/jac/dkh339
JAC vol.54 no.2 © The British Society for Antimicrobial Chemotherapy 2004; all rights reserved.
Selection of resistance of telithromycin against Haemophilus influenzae, Moraxella catarrhalis and streptococci in comparison with macrolides
Laboratory of Clinical Microbiology, Department of Clinical Sciences L. Sacco Teaching Hospital, University of Milan, Via GB Grassi 74, 20157 Milan, Italy
* Corresponding author. Tel: +39-0239042469; Fax: +39-0250319651; Email: microbio{at}unimi.it
Objective: The in vitro abilities of telithromycin, azithromycin and clarithromycin to select for resistance were compared by testing isolates of Haemophilus influenzae, Moraxella catarrhalis, Streptococcus pneumoniae and ß-haemolytic streptococci.
Methods: Five strains each of ß-lactamase-positive and ß-lactamase-negative H. influenzae, ß-lactamase-positive and ß-lactamase-negative M. catarrhalis, S. pneumoniae, ß-haemolytic group A, group C and group G streptococci and three strains of ß-lactamase-negative ampicillin-resistant H. influenzae were evaluated. Development of resistance was determined by multi-step and single-step methodologies. For multi-step studies, MIC values were determined after five serial passages on antibiotic-gradient plates and after 10 serial passages on antibiotic-free plates. Acquisition of resistance was defined as an increase of
4-fold from the starting MIC. In single-step studies, the rate of spontaneous mutations was calculated after a passage on plates containing antibiotics at concentrations equal to the highest NCCLS breakpoints.
Results: Azithromycin, clarithromycin and telithromycin gave a
4-fold increase in 20, 20 and 10 streptococcus strains, in 4, 5 and 0 H. influenzae strains and in 2, 7 and 4 M. catarrhalis strains, respectively. After 10 passages on antibiotic-free plates, 21/26 strains for azithromycin, 22/32 for clarithromycin and 1/14 for telithromycin maintained high MIC values. In single-step studies, the frequency of mutations was <1010 for H. influenzae and M. catarrhalis for telithromycin, azithromycin and clarithromycin. Telithromycin induced mutations at a lower rate than azithromycin and clarithromycin in streptococcal strains.
Conclusion: Telithromycin showed a very limited ability to select for resistance in respiratory pathogens compared with azithromycin and clarithromycin.
Keywords: azithromycin , clarithromycin , ketolides , in vitro selection of resistance , respiratory pathogens
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