Atovaquone resistance in malaria parasites

被引:63
作者
Vaidya, AB [1 ]
Mather, MW [1 ]
机构
[1] Med Coll Penn & Hahnemann Univ, Dept Microbiol & Immunol, Philadelphia, PA 19129 USA
关键词
D O I
10.1054/drup.2000.0157
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Atovaquone is a broad-spectrum antiparasitic agent active against malaria, Pneumocystis carinii pneumonia, toxoplasmosis and babesiosis. When used as a single agent, resistance to atovaquone arose rapidly in falciparum malaria, requiring the development of a new antimalarial drug combination of atovaquone and proguanil. Recent laboratory investigations have provided insights into the mode of atovaquone action, and identified the molecular basis for the resistance development. Mutations within a catalytic domain of the cytochrome be, complex present within the parasite mitochondrial inner membrane were shown to be responsible for atovaquone resistance. Here, we review these studies and propose a mechanism by which atovaquone resistance may arise quickly in malaria parasites. (C) 2000 Harcourt Publishers Ltd.
引用
收藏
页码:283 / 287
页数:5
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