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Antimicrobial Agents and Chemotherapy, Apr 1996, 941-946, Vol 40, No. 4
E Azoulay-Dupuis, P Moine, JP Bedos, V Rieux and E Vallee
We used a mouse model of pneumococcal pneumonia to assess the bactericidal
effect of increasing doses of amoxicillin (AMX) against clinical strains
with various susceptibilities to penicillin. Twelve strains that exhibited
similar virulence in mice were selected. Three were penicillin susceptible
(PS) (penicillin and AMX MICs = 0.01 to 0.03 microgram/ml), three were
intermediately resistant (PIR) (penicillin and AMX MICs = 0.5 to 1
microgram/ml), and six were penicillin resistant (PR) (penicillin and AMX
MICs = 1 to 8 micrograms/ml). Leukopenic Swiss mice were infected
intratracheally with 10(7) CFU of each strain. Treatment was initiated 3 h
after infection and consisted of a single subcutaneous injection of AMX at
doses ranging from 2.5 to 10 mg/kg (PS strains), 5 to 100 (PIR strains),
and 25 to 3,000 (PR strains). Bacterial killing kinetics were recorded in
the lungs over 9 h. The maximal log CFU reduction (Emax) was observed 3 h
postinjection. The relation between Emax and log10(dose/MIC) showed two
populations. With seven strains (the three PS, the three PIR, and one of
the six PR [MICs, penicillin/AMX = 4/1]) a good correlation was observed
between Emax and log10(dose/MIC) (r = 0.772; P < 0.02). A bactericidal
effect equal to 3.5 log10 CFU was observed at a log10(dose/MIC) = 2. At
this ratio, with the five other PR strains, Emax varied from 0.4 to 1.6
log10 CFU. In brain heart infusion medium containing AMX at 50 times the
relevant MIC, these five PR strains were tolerant in vitro. Treatment
failure with AMX was found in vivo, with tolerant, highly resistant
strains.
Copyright © 1996 by the American Society for Microbiology. All rights reserved.
Amoxicillin dose-effect relationship with Streptococcus pneumoniae in a mouse pneumonia model and roles of in vitro penicillin susceptibilities, autolysis, and tolerance properties of the strains
Institut National de la Sante et de la Recherche Medicale U13, Groupe Hospitalier Bichat-Claude Bernard, Paris, France.
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