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Antimicrobial Agents and Chemotherapy, March 2005, p. 996-1001, Vol. 49, No. 3
0066-4804/05/$08.00+0 doi:10.1128/AAC.49.3.996-1001.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.
Pulmonary Damage and Bacterial Load in Assessment of the Efficacy of Simulated Human Treatment-Like Amoxicillin (2,000 Milligrams) Therapy of Experimental Pneumococcal Pneumonia Caused by Strains for Which Amoxicillin MICs Differ
Matilde Gracia,1 Carmina Martínez-Marín,1 Lorena Huelves,1 Maria J. Giménez,2 Lorenzo Aguilar,2 Antonio Carcas,3 Carmen Ponte,1 and Francisco Soriano1*Department of Medical Microbiology, Fundación Jiménez Díaz,1 GlaxoSmithKline,2 Department of Clinical Pharmacology, Hospital La Paz, Madrid, Spain3
Received 23 June 2004/ Returned for modification 29 September 2004/ Accepted 9 November 2004
An experimental rat pneumonia model using two amoxicillin-susceptible (MICs, 
0.015 and 2 µg/ml) and two non-amoxicillin-susceptible (MIC, 4 µg/ml) Streptococcus pneumoniae strains was developed for testing the efficacy of amoxicillin administered to simulate human serum kinetics after treatment with amoxicillin-clavulanate (2,000 and 125 mg, respectively, twice a day, for 2.5 days). The end points for efficacy were reductions in bacterial loads in the lungs and reductions in levels of pulmonary damage. For the amoxicillin-susceptible strains (serotypes 23F and 14), a decrease greater than 4.5 log10 CFU/pair of lungs was obtained, and the time for which the serum antibiotic concentration (SAC) was higher than the MIC (TSAC>MIC) was greater than 60% of the dosing interval. For non-amoxicillin-susceptible strains, the decrease in bacterial load was 1.34 to 1.75 log10 CFU/pair of lungs, with a TSAC>MIC of 46.7% of the dosing interval. An in vitro study showed that serotype 9V non-amoxicillin-susceptible strains behaved as tolerant-like to concentrations similar to those in the in vivo model. The high and maintained SACs (TSAC>MIC, >46% for all strains) significantly diminished lung injury (affected area of the lung and lung weight), compared to that in controls, by all strains, regardless of the MIC, bactericidal behavior in in vitro killing curves, or the serotype of the infecting strain. These results show the importance of host therapeutic end points in the evaluation of antibiotic efficacy. The antibiotic was more efficacious, for one nonsusceptible strain tested, when the treatment was started early (1 h postinoculation [p.i.]) than when treatment was delayed (24 h p.i.).
* Corresponding author. Mailing address: Department of Medical Microbiology, Fundación Jiménez Díaz, Avenida de Reyes Católicos 2, 28040 Madrid, Spain. Phone: 34-91-5447387. Fax: 34-91-5494764. E-mail: fsoriano{at}fjd.es.
Antimicrobial Agents and Chemotherapy, March 2005, p. 996-1001, Vol. 49, No. 3
0066-4804/05/$08.00+0 doi:10.1128/AAC.49.3.996-1001.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.
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