Villarreal Diana, Nirdé Philippe, Hide Mallorie, Barnabé Christian, Tibayrenc Michel
Génétique et Evolution des Maladies Infectieuses G.E.M.I., UMR 2724 CNRS/IRD, UR 165 IRD, Centre de Recherche IRD, 911 avenue Agropolis, BP 64501, 34394 Montpellier Cedex 5, France.
Antimicrob Agents Chemother. 2005 Jul;49(7):2701-9. doi: 10.1128/AAC.49.7.2701-2709.2005.
We analyzed the differential gene expression among representative Trypanosoma cruzi stocks in relation to benznidazole exposures using a random differentially expressed sequences (RADES) technique. Studies were carried out with drug pressure both at the natural susceptibility level of the wild-type parasite (50% inhibitory concentration for the wild type) and at different resistance levels. The pattern of differential gene expression performed with resistant stocks was compared to the population structure of this parasite, established by random amplified polymorphic DNA analysis and multilocus enzyme electrophoresis. A RADES band polymorphism was observed, and over- or underexpression was linked to the resistance level of the stock. The analysis of RADES bands suggested that different products may be involved in benznidazole resistance mechanisms. No significant association was found between phylogenetic clustering and benznidazole susceptibility. Benznidazole resistance may involve several mechanisms, depending on the level of drug exposure.
我们使用随机差异表达序列(RADES)技术分析了代表性克氏锥虫株在接受苯硝唑处理后的差异基因表达情况。研究在野生型寄生虫的自然易感性水平(野生型的50%抑制浓度)以及不同抗性水平的药物压力下进行。将抗性株的差异基因表达模式与通过随机扩增多态性DNA分析和多位点酶电泳确定的该寄生虫的群体结构进行比较。观察到RADES条带多态性,且过表达或低表达与虫株的抗性水平相关。对RADES条带的分析表明,不同产物可能参与苯硝唑抗性机制。系统发育聚类与苯硝唑敏感性之间未发现显著关联。苯硝唑抗性可能涉及多种机制,这取决于药物暴露水平。