Comparison of gene expression patterns among Leishmania braziliensis clinical isolates showing a different in vitro susceptibility to pentavalent antimony

被引:31
作者
Adaui, V. [1 ,2 ]
Schnorbusch, K. [1 ,3 ]
Zimic, M. [4 ]
Gutierrez, A. [4 ]
Decuypere, S. [1 ]
Vanaerschot, M. [1 ,3 ]
De Doncker, S. [1 ]
Maes, I. [1 ]
Llanos-Cuentas, A. [2 ]
Chappuis, F. [5 ]
Arevalo, J. [2 ,4 ]
Dujardin, J-C [1 ,3 ]
机构
[1] Inst Trop Med, Unit Mol Parasitol, Dept Parasitol, B-2000 Antwerp, Belgium
[2] Univ Peruana Cayetano Heredia, Inst Med Trop Alexander von Humboldt, Lima, Peru
[3] Univ Antwerp, Dept Biomed Sci, Fac Pharmaceut Biomed & Vet Sci, B-2020 Antwerp, Belgium
[4] Univ Peruana Cayetano Heredia, Labs Invest & Desarrollo, Fac Ciencias & Filosofia, Lima, Peru
[5] Hop Univ Geneve, Dept Community Med, Geneva, Switzerland
关键词
Leishmania (Viannia) braziliensis; antimony resistance; gene expression profiling; promastigotes; clinical isolates; ORNITHINE-DECARBOXYLASE; DONOVANI; RESISTANCE; METACYCLOGENESIS; OVEREXPRESSION; PROMASTIGOTE; DYNAMICS;
D O I
10.1017/S0031182010001095
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Introduction. Evaluation of Leishmania drug susceptibility depends on in vitro Sb-V susceptibility assays, which are labour-intensive and may give a biased view of the true parasite resistance. Molecular markers are urgently needed to improve and simplify the monitoring of Sb-V-resistance. We analysed here the gene expression profile of 21 L. braziliensis clinical isolates in vitro defined as Sb-V-resistant and -sensitive, in order to identify potential resistance markers. Methods. The differential expression of 13 genes involved in Sb-V metabolism, oxidative stress or housekeeping functions was analysed during in vitro promastigote growth. Results. Expression profiles were up-regulated for 5 genes only, each time affecting a different set of isolates (mosaic picture of gene expression). Two genes, ODC (ornithine decarboxylase) and TRY R (trypanothione reductase), showed a significantly higher expression rate in the group of Sb-V-resistant compared to the group of Sb-V-sensitive parasites (P < 0.01). However, analysis of individual isolates showed both markers to explain only partially the drug resistance. Discussion. Our results might be explained by (i) the occurrence of a pleiotropic molecular mechanism leading to the in vitro Sb-V resistance and/or (ii) the existence of different epi-phenotypes not revealed by the in vitro Sb-V susceptibility assays, but interfering with the gene expression patterns.
引用
收藏
页码:183 / 193
页数:11
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