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Antimicrobial Agents and Chemotherapy, February 1998, p. 352-357, Vol. 42, No. 2
Institut de Chimie des Substances Naturelles,
Received 23 June 1997/Returned for modification 17 November
1997/Accepted 3 December 1997
Amphotericin B (AmB)-resistant Leishmania donovani
promastigotes were selected by increasing drug pressure, and their
biological features were compared with those of the wild-type parent
strain. The 50% inhibitory concentration for resistant cells was 20 times higher than that for the wild-type. Resistance was stable after more than 40 passages in drug-free medium, and resistant promastigotes were infective to macrophages in vitro but lost their virulence in
vivo. They had 2.5 times longer generation time, decreased AmB uptake,
and increased AmB efflux in comparison to the wild type. Fluorescence
measurement with a specific plasma membrane probe,
1-[4-(trimethylammonio)-1,6-diphenylhexa]-1,3,5-triene, showed
increased membrane fluidity in drug-resistant promastigotes. Analysis
of lipid composition showed that in resistant cells saturated fatty
acids were prevalent, with stearic acid as the major fatty acid, and
the major sterol was an ergosterol precursor, the cholesta-5, 7, 24-trien-3
0066-4804/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Mechanism of Amphotericin B Resistance in
Leishmania donovani Promastigotes
-ol and not ergosterol as in the AmB-sensitive strain.
*
Corresponding author. Mailing address: Biologie et
Contrôle des Organismes Parasites, Faculté de Pharmacie,
Université de Paris-Sud, F-92296, Châtenay-Malabry, France.
Phone: 33 1 46 83 55 54. Fax: 33 1 46 83 55 57. E-mail:
philippe.loiseau{at}cep.u-psud.fr.
Antimicrobial Agents and Chemotherapy, February 1998, p. 352-357, Vol. 42, No. 2
0066-4804/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
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