Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5916081 | Molecular and Biochemical Parasitology | 2007 | 11 Pages |
Abstract
Mutations in the Plasmodium falciparum pfcrt gene cause resistance to the 4-amino quinoline chloroquine (CQ) and other antimalarial drugs. Mutations and/or overexpression of a P. falciparum multidrug resistance gene homologue (pfmdr1) may further modify or tailor the degree of quinoline drug resistance. Recently [Ferdig MT, Cooper RA, Mu JB, et al. Dissecting the loci of low-level quinine resistance in malaria parasites. Mol Microbiol 2004;52:985-97] QTL analysis further implicated a region of P. falciparum chromosome 13 as a partner (with pfcrt) in conferring resistance to the first quinoline-based antimalarial drug, quinine (QN). Since QN resistance (QNR) and CQR are often (but not always) observed together in parasite strains, since elevated cytosolic pH is frequently (but not always) found in CQR parasites, and since the chr 13 segment linked to QNR prominently harbors a gene encoding what appears to be a P. falciparum Na+/H+ exchanger (PfNHE), we have systematically measured cytosolic pH and PfNHE activity for an extended series of parasite strains used in the QTL analysis. Altered PfNHE activity does not correlate with CQR as previously proposed, but significantly elevated PfNHE activity is found for strains with high levels of QNR, regardless their CQR status. We propose that either an elevated pHcyt or a higher vacuolar pH-to-cytosolic pH gradient contributes to one common route to malarial QNR that is also characterized by recently defined chr 13-chr 9 pairwise interactions. Based on sequence analysis we propose a model whereby observed polymorphisms in PfNHE may lead to altered Na+/H+ set point regulation in QNR parasites.
Keywords
NMDGPfMDR1PfCRTsDCMP. falciparumamodiaquineNHEQnrCQRBCECF-AMChrPGPCCCPEIPALSCMQTLSCP2′,7′-bis-(2-carboxyethyl)-5-(and-6)-carboxyfluorescein, acetoxymethyl esteriRBCROIMDRPlasmodium falciparum chloroquine resistance transporterBSAP-glycoproteinbovine serum albuminQuantitative trait lociMalariaMultidrug resistancemefloquineregion of interestLaser scanning confocal microscopydigestive vacuoleCarbonyl cyanide 3-chlorophenylhydrazoneChromosomeChloroquineQuinineQuinidineinfected red blood cell
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Authors
Tyler N. Bennett, Jigar Patel, Michael T. Ferdig, Paul D. Roepe,