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Antimicrobial Agents and Chemotherapy, 02 1995, 400-405, Vol 39, No. 2
B Fantin, R Leclercq, Y Merle, L Saint-Julien, C Veyrat, J Duval and C Carbon
In order to determine the microbiological and pharmacokinetic parameters
that best predicted the in vivo antistaphylococcal activity of the
streptogramin RP 59500 (quinupristin-dalfopristin), we evaluated the
activity in rabbit aortic endocarditis of three regimens of
quinupristin-dalfopristin against five strains of Staphylococcus aureus
with various streptogramin B-type antibiotic resistance phenotypes and
susceptible to streptogramin A-type antibiotics. Quinupristin- dalfopristin
was as active as vancomycin against three strains that were susceptible to
its streptogramin B component quinupristin, including one strain that was
inducibly resistant to erythromycin, but had a significantly decreased
activity against two strains that were resistant to quinupristin, for all
quinupristin-dalfopristin regimens tested (P < 0.05). The area under the
concentration-time curve for quinupristin-dalfopristin in plasma divided by
the MIC of quinupristin was the only parameter retained by multilinear
regression that predicted the in vivo activity of quinupristin-dalfopristin
(P = 0.0001), emphasizing the importance of determining the susceptibility
to quinupristin in order to predict the in vivo activity of
quinupristin-dalfopristin against S. aureus.
Copyright © 1995 by the American Society for Microbiology. All rights reserved.
Critical influence of resistance to streptogramin B-type antibiotics on activity of RP 59500 (quinupristin-dalfopristin) in experimental endocarditis due to Staphylococcus aureus
Institut National de la Sante et de la Recherche Medicale, Unite 13, Paris, France.
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