Fig. 6: Model for involvement of pfaat1 haplotypes in CQ resistance and fitness. | Nature Microbiology

Fig. 6: Model for involvement of pfaat1 haplotypes in CQ resistance and fitness.

From: Chloroquine resistance evolution in Plasmodium falciparum is mediated by the putative amino acid transporter AAT1

Fig. 6

pfCRT (red) and pfAAT1 (blue) are both situated in the digestive vacuole (DV) membrane. a, WT pfCRT and pfAAT1 transport peptides and aromatic amino acids, respectively, as well as CQ. b, pfCRT K76T exports CQ from the DV away from its site of action, leading to elevated resistance but transports peptides inefficiently leading to a loss of fitness. c, pfAAT1 S258L reduces entry of CQ into the DV, leading to elevated resistance, but amino acid flux is affected, leading to a loss of fitness. d, The pfAAT1 S258L/F313S double mutation increases CQ influx in comparison with the S258L alone but the amino acid transport function is restored, leading to reduced IC50 values and increased fitness in the absence of drug treatment.

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