Choudhury Kohelia, Zander Dorothea, Kube Michael, Reinhardt Richard, Clos Joachim
Bernhard Nocht Institute for Tropical Medicine, RG Leishmaniasis, Bernhard Nocht St 74, D-20359 Hamburg, Germany.
Int J Parasitol. 2008 Oct;38(12):1411-23. doi: 10.1016/j.ijpara.2008.03.005. Epub 2008 Apr 8.
Resistance to treatment is a growing problem in efforts to control Old World leishmaniasis. Parasites resistant to new therapeutics such as miltefosine have not been reported from the field yet but based on experimental evidence, may appear soon. Therefore, we attempted to identify genetic markers that may correlate with miltefosine resistance. Using a functional cloning approach, we have isolated a gene from Leishmania infantum that, upon over-expression, confers protection not only against miltefosine, but also against Sb(III), the active principle of anti-leishmanial antimonials. The gene encodes a very large putative polypeptide of 299 kDa that shows no similarities to known proteins or functional motifs. Database mining and karyotyping experiments suggest that in L. infantum this gene is part of a 44-kbp duplicated region that is found on two separate chromosomes, CHR08 and CHR29.
在控制东半球利什曼病的努力中,治疗耐药性问题日益严重。对诸如米替福新等新疗法具有抗性的寄生虫尚未在野外被报道,但基于实验证据,可能很快就会出现。因此,我们试图鉴定可能与米替福新抗性相关的遗传标记。使用功能克隆方法,我们从婴儿利什曼原虫中分离出一个基因,该基因在过表达时不仅赋予对米替福新的抗性,还赋予对三价锑(抗利什曼病锑剂的活性成分)的抗性。该基因编码一个299 kDa的非常大的推定多肽,与已知蛋白质或功能基序没有相似性。数据库挖掘和核型分析实验表明,在婴儿利什曼原虫中,该基因是一个44 kbp重复区域的一部分,该区域位于两条不同的染色体CHR08和CHR29上。