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. Author manuscript; available in PMC: 2023 Jan 18.
Published in final edited form as: Curr Opin Microbiol. 2022 Aug 22;69:102193. doi: 10.1016/j.mib.2022.102193

Table 2.

Molecular markers of antimalarial drug resistance in P. falciparum.

Class Drug Gene (s) Mutation
4-aminoquinolines Chloroquine pfcrt Necessary but not sufficient: K76Ta
Other mutations include C72S, M74I, N75E, A220S, Q271E, N326S, I356T, and R371I
pfmdrl (in combination with mutant pfcrt only) N86Y, Y184F, S1034C, N1042D, and D1246Y
Amodiaquine pfcrt and pfmdrl PfMDR1 N86Y and PfCRT K76T contribute to decreased parasite susceptibility
Piperaquine pm2/3 Increased copy number
pfcrt T93S, H97Y, F145I, I218F, M343L, C350R, or G353V
Pyronaridine Yet to be identified -
Amino alcohols Lumefantrine Yet to be identified Selects for PfMDR1 N86 and PfCRT K76
Mefloquine pfmdrl Increased copy number
Endoperoxide Artemisinin derivatives k13 Validated: P413A, F446I, N458Y, C469Y, M476I, Y493H, R539T, I543T, P553L, R561H, P574L, C580Y, and A675Vb
Candidate or associated: P441L, G449A, C469F, A481V, R515K, P527H, N537I/D, G538V, and R622I
a

Chloroquine resistance requires at least four mutations that include K76T.

b

Validated K13 markers have a statistically significant association between the mutation and delayed clearance as well as survival > 1% in the ring-stage survival assay. Candidate or associated markers fulfill one of these conditions to date.