| Literature DB >> 26711753 |
David L Saunders1, Suwanna Chaorattanakawee2, Panita Gosi2, Charlotte Lanteri2, Sok Somethy3, Worachet Kuntawunginn2, Mali Ittiverakul2, Soklyda Chann4, Carrie Gregory2, Char Meng Chuor5, Satharath Prom3, Michele D Spring2, Chanthap Lon4.
Abstract
Our recent report of dihydroartemisinin-piperaquine failure to treat Plasmodium falciparum infections in Cambodia adds new urgency to the search for alternative treatments. Despite dihydroartemisinin-piperaquine failure, and higher piperaquine 50% inhibitory concentrations (IC50s) following reanalysis than those previously reported, P. falciparum remained sensitive to atovaquone (ATQ) in vitro. There were no point mutations in the P. falciparum cytochrome b ATQ resistance gene. Mefloquine, artemisinin, chloroquine, and quinine IC50s 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.Entities:
Mesh:
Substances:
Year: 2015 PMID: 26711753 PMCID: PMC4775999 DOI: 10.1128/AAC.02302-15
Source DB: PubMed Journal: Antimicrob Agents Chemother ISSN: 0066-4804 Impact factor: 5.191