Small-Molecule Xenomycins Inhibit All Stages of the Plasmodium Life Cycle

被引:11
|
作者
Erath, Jessey [1 ]
Gallego-Delgado, Julio [1 ]
Xu, Wenyue [1 ]
Andriani, Grasiella [1 ]
Tanghe, Scott [1 ]
Gurova, Katerina V. [2 ]
Gudkov, Andrei [2 ]
Purmal, Andrei [3 ]
Rydkina, Elena [2 ]
Rodriguez, Ana [1 ]
机构
[1] NYU, Sch Med, Dept Microbiol, Div Parasitol, New York, NY 10016 USA
[2] Roswell Pk Canc Inst, Dept Cell Stress Biol, Buffalo, NY 14263 USA
[3] Incuron LLC, Buffalo, NY USA
关键词
MALARIA; ERADICATION;
D O I
10.1128/AAC.04704-14
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Widespread resistance to most antimalaria drugs in use has prompted the search for novel candidate compounds with activity against Plasmodium asexual blood stages to be developed for treatment. In addition, the current malaria eradication programs require the development of drugs that are effective against all stages of the parasite life cycle. We have analyzed the antimalarial properties of xenomycins, a novel subclass of small molecule compounds initially isolated for anticancer activity and similarity to quinacrine in biological effects on mammalian cells. In vitro studies show potent activity of Xenomycins against Plasmodium falciparum. Oral administration of xenomycins in mouse models result in effective clearance of liver and blood asexual and sexual stages, as well as effective inhibition of transmission to mosquitoes. These characteristics position xenomycins as antimalarial candidates with potential activity in prevention, treatment and elimination of this disease.
引用
收藏
页码:1427 / 1434
页数:8
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