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. 2016 Jul 22;60(8):5010–5013. doi: 10.1128/AAC.03105-15

TABLE 1.

Ex vivo susceptibility of 40 Plasmodium falciparum isolates to chloroquine, quinine, monodesethylamodiaquine, mefloquine, lumefantrine, piperaquine, pyronaridine, dihydroartemisinin, artesunate, and doxycycline according to the D113N mutation in the E3 ubiquitin protein ligase genea

Drug Wild-type D113N (no. of isolates)
Mutated D113N (no. of isolates)
P value
Mean IC50 95% CI Mean IC50 95% CI
CQ 75.8 nM (15) 43.9–130.8 60.5 nM (25) 40.4–89.3 0.3909
QN 116.2 nM (15) 64.6–209.0 71.4 nM (24) 42.0–121.2 0.4188
DQ 23.5 nM (15) 12.0–46.2 17.1 nM (25) 10.2–28.7 0.4178
MQ 22.4 nM (14) 15.3–32.8 27.5 nM (25) 19.0–39.8 0.2887
LMF 6.6 nM (15) 3.3–13.6 5.7 nM (25) 3.3–9.8 0.6711
PPQ 34.5 nM (13) 27.1–43.9 37.7 nM (25) 23.0–61.9 0.5827
PND 10.3 nM (13) 7.6–13.9 9.7 nM (20) 5.8–16.2 0.6717
DHA 1.6 nM (14) 0.9–2.7 1.4 nM (25) 0.7–2.6 0.9883
AS 3.3 nM (13) 1.9–5.7 2.2 nM (19) 1.2–4.1 0.2872
DOX 12.2 μM (14) 6.7–22.3 13.6 μM (25) 8.4–22.1 0.6539
a

CQ, chloroquine; QN, quinine; DQ, monodesethylamodiaquine; MQ, mefloquine; LMF, lumefantrine; PPQ, piperaquine; PND, pyronaridine; DHA, dihydroartemisinin; AS, artesunate; DOX, doxycycline; mean IC50, geometric mean 50% inhibitory concentration; 95% CI, 95% confidence interval. P values were determined by the Wilcoxon signed-rank test.