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Microbiology 145 (1999), 2527-2532
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Microbiology (1999), 145, 2527-2532.
© 1999 Society for General Microbiology


Biochemistry

Purification and inhibition by quinolones of DNA gyrases from Mycobacterium avium, Mycobacterium smegmatis and Mycobacterium fortuitum bv. peregrinum

Isabelle Guillemin1, Wladimir Sougakoff1, Emmanuelle Cambau1, Valérie Revel-Viravau1, Nicole Moreau2 and Vincent Jarlier1

Laboratoire de Recherche Moléculaire sur les Antibiotiques (LRMA), Université Pierre et Marie Curie (Paris VI), Faculté de Médecine Pitié-Salpêtrière, 91 Bd de l’Hôpital, 75634 Paris Cédex 13, France1
LRMA, Faculté de Médecine, Broussais-Hôtel Dieu, 75005 Paris, France2

Author for correspondence: Wladimir Sougakoff. Tel: +33 1 40 77 97 46. Fax: +33 1 45 82 75 77. e-mail: sougakof@ lmcp.jussieu.fr

The DNA gyrases from Mycobacterium avium, Mycobacterium smegmatis and Mycobacterium fortuitum bv. peregrinum, which are species naturally resistant, moderately susceptible and susceptible to fluoroquinolones, respectively, were purified by affinity chromatography on novobiocin-Sepharose columns. The DNA gyrase inhibiting activities (IC50 values) of classical quinolones and fluoroquinolones were determined from the purified enzymes and were compared to the corresponding antibacterial activities (MICs). Regarding M. fortuitum bv. peregrinum, which is nearly as susceptible as Escherichia coli, the corresponding MIC and IC50 values of quinolones were significantly lower than those found for M. avium and M. smegmatis (e.g. for ofloxacin, MICs of 0·25 versus 32 and 1 µg ml-1, and IC50 values of 1 versus 8 and 6 µg ml-1, respectively). Such a result could be related to the presence of Ser-83 in the quinolone-resistance-determining region of the gyrase A subunit of M. fortuitum bv. peregrinum, as found in wild-type E. coli, instead of Ala-83 in M. avium and M. smegmatis, as found in fluoroquinolone-resistant E. coli mutants. The IC50 values of quinolones against the M. avium and M. smegmatis DNA gyrases were similar, while the corresponding MICs were 32-fold higher for M. avium when compared to M. smegmatis, suggesting that an additional mechanism, such as a low cell wall permeability or a drug efflux, could contribute to the low antibacterial potency of quinolones against M. avium.

Keywords: Mycobacterium, DNA gyrase, quinolone inhibition assays, fluoroquinolone resistance

Abbreviations: QRDR, quinolone-resistance-determining regions




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