Activity of subinhibitory concentrations of dapsone alone and in combination with cell-wall inhibitors against Mycobacterium avium complex organisms.
N Rastogi, K S Goh, V Labrousse
Index: Eur. J. Clin. Microbiol. Infect. Dis. 12(12) , 954-8, (1993)
Full Text: HTML
Abstract
MICs of dapsone (p-p'-diaminodiphenylsulfone) were determined radiometrically for ten strains each of the Mycobacterium avium complex (MAC) and Mycobacterium tuberculosis. MICs ranged from 50 to 250 micrograms/ml for Mycobacterium tuberculosis and from 2 to 100 micrograms/ml for MAC. However, at a concentration as low as 1.5 micrograms/ml dapsone significantly inhibited growth of MAC bacteria when used in combination with other drugs specifically acting at the mycobacterial cell-wall level. The latter drugs were used in subinhibitory concentrations, and included m-fluorophenylalanine (an inhibitor of mycoside-C biosynthesis), ethambutol (an inhibitor of arabinogalactan biosynthesis), and ethionamide (an inhibitor of mycolic acid biosynthesis). Using a radiometric method (Bactec 460-TB), the activity of dapsone was found to be enhanced for 2/10 strains in the presence of m-fluorophenylalanine, for 3/10 strains in the presence of ethambutol and for 5/10 strains in the presence of ethionamide. A satisfactory correlation between the radiometric data and bacterial viable counts was established.
Related Compounds
Related Articles:
Hidden overflow pathway to L-phenylalanine in Pseudomonas aeruginosa.
1983-05-01
[J. Bacteriol. 154(2) , 623-31, (1983)]
1992-10-15
[Biochem. J. 287 ( Pt 2) , 627-32, (1992)]
1994-05-03
[Biochemistry 33(17) , 5238-45, (1994)]
Fungitoxicity of m-fluorophenylalanine-containing peptides towards Pythium ultimum.
1989-04-15
[Experientia 45(4) , 325-7, (1989)]
2009-09-15
[Bioorg. Med. Chem. Lett. 19(18) , 5449-51, (2009)]