Antimicrob Agents Chemother
We have analyzed the in vitro chemosensitivity profiles of 115 Kenyan isolates for chloroquine (CQ), piperaquine, lumefantrine (LM), and dihydroartemisinin in association with polymorphisms in pfcrt at codon 76 and pfmdr1 at codon 86, as well as with variations of the copy number of pfmdr1. The median drug concentrations that inhibit 50% of parasite growth (IC(50)s) were 41 nM (interquartile range [IQR], 18 to 73 nM), 50 nM (IQR, 29 to 96 nM), 32 nM (IQR, 17 to 46 nM), and 2 nM (IQR, 1 to 3 nM) for CQ, LM, piperaquine, and dihydroartemisinin, respectively. The activity of CQ correlated inversely with that of LM (r(2) = -0.26; P = 0.02). Interestingly, parasites for which LM IC(50)s were higher were wild type for pfcrt-76 and pfmdr1-86. All isolates had one pfmdr1 copy. Thus, the decrease in LM activity is associated with the selection of wild-type pfcrt-76 and pfmdr1-86 parasites, a feature that accounts for the inverse relationship between CQ and LM. Therefore, the use of LM-artemether is likely to lead to the selection of more CQ-susceptible parasites.
Mwai, L., Kiara, S. M., Abdirahman, A., Pole, L., Rippert, A., Diriye, A., Bull, P., Marsh, K., Borrmann, S., Nzila, A.
Pages:5069-73, Volume:53, Edition:9/23/2009, Date,Dec
Notes:Mwai, Leah|Kiara, Steven M|Abdirahman, Abdi|Pole, Lewa|Rippert, Anja|Diriye, Abdi|Bull, Pete|Marsh, Kevin|Borrmann, Steffen|Nzila, Alexis|WT077092/Wellcome Trust/United Kingdom|WT084538/Wellcome Trust/United Kingdom|Research Support, Non-U.S. Gov’t|United States|Antimicrobial agents and chemotherapy|Antimicrob Agents Chemother. 2009 Dec;53(12):5069-73. doi: 10.1128/AAC.00638-09. Epub 2009 Sep 21.
ISBN: 1098-6596 (Electronic)|0066-4804 (Linking) Permanent ID: 2786317 Accession Number: 19770282
Author Address: Kenya Medical Research Institute (KEMRI)/Wellcome Trust Collaborative Research Program, Kilifi, Kenya.