Axenically grown amastigotes of Leishmania infantum used as an in vitro model to investigate the pentavalent antimony mode of action

被引:120
作者
Sereno, D
Cavaleyra, M
Zemzoumi, K
Maquaire, S
Ouaissi, A
Lemesre, JL
机构
[1] Ctr ORSTOM, Lab Biol Parasitaire, F-34032 Montpellier 1, France
[2] Ctr ORSTOM, INSERM, CJF 96 04, F-34032 Montpellier, France
关键词
D O I
10.1128/AAC.42.12.3097
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The mechanism(s) of activity of pentavalent antimony [Sb(V)] is poorly understood, In a recent study, we have shown that potassium antimonyl tartrate, a trivalent antimonial [Sb(III)], was substantially more potent than Sb(V) against both promastigotes and axenically grown amastigotes of three Leishmania species, supporting the idea of an in vivo metabolic conversion of Sb(V) into Sb(III), We report that amastigotes of Leishmania infantum cultured under axenic conditions were poorly susceptible to meglumine [Glucantime; an Sb(V)], unlike those growing inside THP-1 cells (50% inhibitory concentrations [IC(50)s], about 1.8 mg/ml and 22 mu g/ml, respectively). In order to define more precisely the mode of action of Sb(V) agents in vivo, we first induced in vitro Sb(III) resistance by direct drug pressure on axenically grown amastigotes of L. infantum. Then we determined the susceptibilities of both extracellular and intracellular chemoresistant amastigotes to the Sb(V)-containing drugs meglumine and sodiun stibogluconate plus m-chlorocresol (Pentostam), The chemoresistant amastigotes LdiR2, LdiR10, and LdiR20 were 14, 26, and 32 times more resistant to Sb(III), respectively, than the wild-type one (LdiWT), In accordance with the hypothesis described above, we found that intracellular chemoresistant amastigotes were resistant to meglumine [Sb(V)] in proportion to the initial level of Sb(III)-induced resistance. By contrast, Sb(III)-resistant cells were very susceptible to sodium stibogluconate, This lack of cross-resistance is probably due to the presence in this reagent of m-chlorocresol, which we found to be more toxic than Sb(III) to L. infantum amastigotes (IC(50)s, of 0.54 and 1.32 mu g/ml, respectively). Collectively, these results were consistent with the hypothesis of an intramacrophagic metabolic conversion of Sb(V) into trivalent compounds, which in turn became readily toxic to the Leishmania amastigote stage.
引用
收藏
页码:3097 / 3102
页数:6
相关论文
共 39 条
[31]   ANTIMONY QUANTIFICATION IN LEISHMANIA BY ELECTROTHERMAL ATOMIC-ABSORPTION SPECTROSCOPY [J].
ROBERTS, WL ;
RAINEY, PM .
ANALYTICAL BIOCHEMISTRY, 1993, 211 (01) :1-6
[32]   Use of an enzymatic micromethod to quantify amastigote stage of Leishmania amazonensis in vitro [J].
Sereno, D ;
Lemesre, JL .
PARASITOLOGY RESEARCH, 1997, 83 (04) :401-403
[33]   Axenically cultured amastigote forms as an in vitro model for investigation of antileishmanial agents [J].
Sereno, D ;
Lemesre, JL .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1997, 41 (05) :972-976
[34]   In vitro life cycle of pentamidine-resistant amastigotes: Stability of the chemoresistant phenotypes is dependent on the level of resistance induced [J].
Sereno, D ;
Lemesre, JL .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1997, 41 (09) :1898-1903
[35]   Phenotypic characterization of Leishmania mexicana pentamidine-resistant promastigotes. Modulation of the resistance during developmental life cycle [J].
Sereno, D ;
Michon, P ;
Brajon, N ;
Lemesre, JL .
COMPTES RENDUS DE L ACADEMIE DES SCIENCES SERIE III-SCIENCES DE LA VIE-LIFE SCIENCES, 1997, 320 (12) :981-987
[36]  
TSUCHIYA S, 1982, CANCER RES, V42, P1530
[37]   MULTIDRUG-RESISTANCE AND P-GLYCOPROTEINS IN PARASITIC PROTOZOA [J].
ULLMAN, B .
JOURNAL OF BIOENERGETICS AND BIOMEMBRANES, 1995, 27 (01) :77-84
[38]   LEISHMANIA-DONOVANI - ISOLATION AND CHARACTERIZATION OF SODIUM STIBOGLUCONATE (PENTOSTAM)-RESISTANT CELL-LINES [J].
ULLMAN, B ;
CARREROVALENZUELA, E ;
COONS, T .
EXPERIMENTAL PARASITOLOGY, 1989, 69 (02) :157-163
[39]   Disposition of antimony after the administration of N-methylglucamine antimoniate to dogs [J].
Valladares, JE ;
Alberola, J ;
Esteban, M ;
Arboix, M .
VETERINARY RECORD, 1996, 138 (08) :181-183