Laurent Thierry, Rijal Suman, Yardley Vanessa, Croft Simon, De Doncker Simonne, Decuypere Saskia, Khanal Basudha, Singh Rupa, Schönian Gabriele, Kuhls Katrin, Chappuis François, Dujardin Jean-Claude
Department of Parasitology, Unit of Molecular Parasitology, Institute of Tropical Medicine, Antwerp B-2000, Belgium.
Infect Genet Evol. 2007 Mar;7(2):206-12. doi: 10.1016/j.meegid.2006.08.005. Epub 2006 Sep 27.
Pentavalent antimonials (SbV) are the first line drug against leishmaniasis worldwide, but drug resistance is increasingly reported, particularly in the Indian sub-continent, where it represents a major threat for the control of anthroponotic visceral leishmaniasis (VL). In order to understand the epidemiological dynamics of antimonial resistance in anthroponotic VL, we analysed here the population structure of 24 Leishmania donovani stocks isolated from anthroponotic VL-patients from Eastern Nepal: 13 SbV-naturally resistant and 11 SbV-sensitive, as demonstrated by in vitro drug susceptibility assays. The parasites were genotyped by PCR-RFLP analysis of kDNA minicircles and by microsatellite analysis and the encountered polymorphism revealed a polyclonal structure among resistant isolates. Furthermore, analysis of paired samples obtained from the same patients before treatment and after failure revealed primary as well as acquired resistance. The hypothesis of independent events of drug resistance emergence is proposed and confronted to alternative explanations. Our results show the dynamics of drug resistance epidemiology and highlight the importance of surveillance networks.
五价锑剂(SbV)是全球治疗利什曼病的一线药物,但耐药情况的报道日益增多,尤其是在印度次大陆,这对控制人源性内脏利什曼病(VL)构成了重大威胁。为了解人源性VL中锑剂耐药的流行病学动态,我们在此分析了从尼泊尔东部人源性VL患者中分离出的24株杜氏利什曼原虫的种群结构:通过体外药敏试验证明,其中13株对SbV天然耐药,11株对SbV敏感。通过对kDNA小环进行PCR-RFLP分析和微卫星分析对寄生虫进行基因分型,所发现的多态性表明耐药分离株具有多克隆结构。此外,对同一患者治疗前和治疗失败后采集的配对样本进行分析,发现了原发性耐药以及获得性耐药。我们提出了耐药性出现的独立事件假说,并与其他解释进行了对比。我们的结果显示了耐药性流行病学的动态变化,并突出了监测网络的重要性。