Atovaquone-Proguanil Remains a Potential Stopgap Therapy for Multidrug-Resistant Plasmodium falciparum in Areas along the Thai-Cambodian Border
Author(s) -
David Saunders,
Suwanna Chaorattanakawee,
Panita Gosi,
Charlotte Lanteri,
Somethy Sok,
Worachet Kuntawunginn,
Mali Ittiverakul,
Soklyda Chann,
Carrie Gregory,
Char Meng Chuor,
Satharath Prom,
Michele Spring,
Chanthap Lon
Publication year - 2015
Publication title -
antimicrobial agents and chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.07
H-Index - 259
eISSN - 1070-6283
pISSN - 0066-4804
DOI - 10.1128/aac.02302-15
Subject(s) - piperaquine , atovaquone , mefloquine , plasmodium falciparum , medicine , artemisinin , dihydroartemisinin , primaquine , pharmacology , proguanil , virology , malaria , chloroquine , immunology
Our recent report of dihydroartemisinin-piperaquine failure to treatPlasmodium falciparum infections in Cambodia adds new urgency to the search for alternative treatments. Despite dihydroartemisinin-piperaquine failure, and higher piperaquine 50% inhibitory concentrations (IC50 s) following reanalysis than those previously reported,P. falciparum remained sensitive to atovaquone (ATQ)in vitro . There were no point mutations in theP. falciparum cytochromeb ATQ resistance gene. Mefloquine, artemisinin, chloroquine, and quinine IC50 s remained comparable to those from other recent reports. Atovaquone-proguanil may be a useful stopgap but remains susceptible to developing resistance when used as blood-stage therapy.
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