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Use of Leishmania donovani Field Isolates Expressing the Luciferase Reporter Gene in In Vitro Drug Screening†

机译:在体外药物筛选中使用表达荧光素酶报告基因的利什曼原虫野外分离株†

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摘要

Currently available primary screens for the selection of candidate antileishmanial compounds are not ideal. These techniques are time-consuming, laborious, and difficult to scale and require macrophages, which limit their use for high-throughput screening. We have developed Leishmania donovani field isolates that constitutively express the firefly luciferase reporter gene (luc) as a part of an episomal vector. An excellent correlation between parasite number and luciferase activity was observed. luc expression was stable, even in the absence of drug selection, for 4 weeks. The transfectants were infective to macrophages, and intracellular amastigotes exhibited luciferase activity. The suitability of these recombinant field isolates for in vitro screening of antileishmanial drugs was established. The luciferase-expressing sodium stibogluconate-resistant cell lines offer a model for the screening of compounds for resistance. The system is in routine use at the Central Drug Research Institute, Lucknow, India, for high-throughput screening of newly synthesized compounds.
机译:当前可用的用于筛选候选抗疟原虫化合物的初级筛选并不理想。这些技术耗时,费力并且难以规模化并且需要巨噬细胞,这限制了它们用于高通量筛选的用途。我们已经开发了组成型表达萤火虫荧光素酶报道基因(luc)作为附加型载体一部分的利什曼原虫多诺万尼(Leishmania donovani)场分离株。观察到寄生虫数量和荧光素酶活性之间的极好的相关性。即使没有药物选择,luc表达也稳定了4周。转染子感染巨噬细胞,胞内变形虫表现出萤光素酶活性。确定了这些重组野外分离株在体外筛选抗疟疾药物的适用性。表达荧光素酶的抗葡糖苷酸钠细胞系为筛选抗药性化合物提供了模型。该系统已在印度拉克瑙的中央药物研究所常规使用,用于高通量筛选新合成的化合物。

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