The present study, using an in vitro model, assessed telithromycin pharmacodynamic activity at simulated clinically achievable free-drug concentrations in serum (S) and epithelial lining fluid (ELF) against efflux (mefE)-producing macrolide-resistant Streptococcus pneumoniae. Two macrolide-susceptible (PCR negative for both mefE and ermB) and 11 efflux-producing macrolide-resistant [PCR-positive for mefE and negative for ermB) S. pneumoniae strains with various telithromycin MICs (0.015 to 1 g/ml) were tested. The steady-state pharmacokinetics of telithromycin were modeled, simulating a dosage of 800 mg orally once daily administered at time 0 and at 24 h (free-drug maximum concentration [C max ] in serum, 0.7 g/ml; half-life [t 1/2 ], 10 h; free-drug C max in ELF, 6.0 g/ml; t 1/2 , 10 h). Starting inocula were 10 6 CFU/ml in Mueller-Hinton Broth with 2% lysed horse blood. Sampling at 0, 2, 4, 6, 12, 24, and 48 h assessed the extent of bacterial killing (decrease in log 10 CFU/ml versus initial inoculum). Free-telithromycin concentrations in serum achieved in the model were C max 0.9 ؎ 0.08 g/ml, area under the curve to MIC (AUC 0-24 h ) 6.4 ؎ 1.5 g · h/ml, and t 1/2 of 10.6 ؎ 0.6 h. Telithromycin-free ELF concentrations achieved in the model were C max 6.6 ؎ 0.8 g/ml, AUC 0-24 h 45.5 ؎ 5.5 g · h/ml, and t 1/2 of 10.5 ؎ 1.7 h. Free-telithromycin S and ELF concentrations rapidly eradicated efflux-producing macrolide-resistant S. pneumoniae with telithromycin MICs up to and including 0.25 g/ml and 1 g/ml, respectively. Free-telithromycin S and ELF concentrations simulating C max /MIC > 3.5 and AUC 0-24 h /MIC > 25 completely eradicated (>4 log 10 killing) macrolide-resistant S. pneumoniae at 24 and 48 h. Free-telithromycin concentrations in serum simulating C max /MIC > 1.8 and AUC 0-24 h /MIC > 12.5 were bacteriostatic (0.1 to 0.2 log 10 killing) against macrolide-resistant S. pneumoniae at 24 and 48 h. In conclusion, free-telithromycin concentrations in serum and ELF simulating C max /MIC > 3.5 and AUC 0-24 h /MIC > 25 completely eradicated (>4 log 10 killing) macrolide-resistant S. pneumoniae at 24 and 48 h.Macrolide (azithromycin, clarithromycin, and erythromycin) resistance in Streptococcus pneumoniae is presently ϳ25% in the United States and approximately 13% in Canada (1,3,28,31). Macrolide resistance in S. pneumoniae involves alteration of the ribosomal target site or production and utilization of an efflux mechanism (6, 9, 29, 33). The production of ribosomal methylase, which alters the ribosomal target site of the macrolide, is usually coded for by the ermB gene and confers broad macrolide, lincosamide, and streptogramin B resistance (6, 9, 29, 33). The second mechanism, which results in macrolide efflux, is coded by the mefA or mefE genes (6,9,29,33). Efflux is macrolide specific (14-and 15-membered macrolides only) and does not affect the lincosamide or streptogramins (28,32). Note that ermB-positive S. pneumoniae strains generally exhibit high-level (MIC 90 Ն 64 g/ml) macrolide resistance, while mefA...