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Ethambutol potentiates extracellular and intracellular activities of clarithromycin,sparfloxacin, amikacin,and rifampin againstMycobacterium avium
Authors:Nalin Rastogi  Valérie Labrousse  Joao Paulo Carvalho de Sousa
Institution:(1) Tuberculosis and Mycobacteria Unit, Institut Pasteur, 25 Rue du Dr. Roux, 75724 Paris, France
Abstract:Intracellular bactericidal activities of the antituberculosis drugs rifampin and amikacin, as well as those of newly described drugs clarithromycin (a macrolide) and sparfoxacin (a difluoroquinolone), were assessed against three strains of theMycobacterium avium complex (MAC) growing in two different in vitro macrophage systems, namely, mouse bone marrowderived macrophages (BMMØ) and human peripheral blood monocyte-derived macrophages (human MØ). All the infected macrophages were fed reported Cmax concentrations of the drugs, i.e., 15mgrg/ml for rifampin, 20 mgrg/ml for amikacin, 4mgrg/ml for clarithromycin, and 1.5mgrg/ml for sparfloxacin. Further potentiation of drug activity in the presence of Cmax level of ethambutol (6mgrg/ml) during 9 days of intracellular growth (measured by lysing the macrophages and making bacterial counts) was assessed. Our results showed that all four drugs were active against the strains used in this study and that the addition of ethambutol (which had no significant intracellular activity against the bacteria in this system) further potentiated the bactericidal effect of the drugs. When the same drug combinations were tested at their sublethal concentrations by BACTEC® radiometric methodology, a good correlation between the drug enhancement data in extracellular and intracellular systems was found. We conclude that ethambutol may serve as an essential component in effective anti-M. avium chemotherapy and that the effective drug combinations may be routinely screened by the Bactec radiometric methodology.
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