Plasmodium dihydrofolate reductase is a second enzyme target for the antimalarial action of triclosan.

Plasmodium dihydrofolate reductase is a second enzyme target for the antimalarial action of triclosan.
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二氢叶酸还原酶是三氯生的抗疟疾作用的第二个酶靶标。

DOI:
10.1038/s41598-018-19549-x
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发表时间:
2018-01-18
期刊:
影响因子:
4.6
通讯作者:
Oliver SG
Oliver SG
中科院分区:
综合性期刊3区
文献类型:
--
作者:
Bilsland E;van Vliet L;Williams K;Feltham J;Carrasco MP;Fotoran WL;Cubillos EFG;Wunderlich G;Grøtli M;Hollfelder F;Jackson V;King RD;Oliver SG

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Malaria, caused by parasites of the genus Plasmodium, leads to over half a million deaths per year, 90% of which are caused by Plasmodium falciparum. P. vivax usually causes milder forms of malaria; however, P. vivax can remain dormant in the livers of infected patients for weeks or years before re-emerging in a new bout of the disease. The only drugs available that target all stages of the parasite can lead to severe side effects in patients with glucose-6-phosphate dehydrogenase (G6PD) deficiency; hence, there is an urgent need to develop new drugs active against blood and liver stages of the parasite. Different groups have demonstrated that triclosan, a common antibacterial agent, targets the Plasmodium liver enzyme enoyl reductase. Here, we provide 4 independent lines of evidence demonstrating that triclosan specifically targets both wild-type and pyrimethamine-resistant P. falciparum and P. vivax dihydrofolate reductases, classic targets for the blood stage of the parasite. This makes triclosan an exciting candidate for further development as a dual specificity antimalarial, which could target both liver and blood stages of the parasite.
DOI: 10.1371/journal.pntd.0001320
发表时间: 2011-10
影响因子: 3.8
作者:
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