Document Type

Article

Publication Date

2010

DOI

10.1111/j.1365-2958.2010.07366.x

Publication Title

Molecular Microbiology

Volume

78

Issue

3

Pages

770-787

Abstract

Mutations in the Plasmodium falciparum chloroquine (CQ) resistance transporter (PfCRT) are major determinants of verapamil (VP)-reversible CQ resistance (CQR). In the presence of mutant PfCRT, additional genes contribute to the wide range of CQ susceptibilities observed. It is not known if these genes influence mechanisms of chemosensitization by CQR reversal agents. Using quantitative trait locus (QTL) mapping of progeny clones from the HB3 x Dd2 cross, we show that the P. falciparum multidrug resistance gene 1 (pfmdr1) interacts with the South-East Asia-derived mutant pfcrt haplotype to modulate CQR levels. A novel chromosome 7 locus is predicted to contribute with the pfcrt and pfmdr1 loci to influence CQR levels. Chemoreversal via a wide range of chemical structures operates through a direct pfcrt-based mechanism. Direct inhibition of parasite growth by these reversal agents is influenced by pfcrt mutations and additional loci. Direct labelling of purified recombinant PfMDR1 protein with a highly specific photoaffinity CQ analogue, and lack of competition for photo labelling by VP, supports our QTL predictions. We find no evidence that pfmdr1 copy number affects CQ response in the progeny; however, inheritance patterns indicate that an allele-specific interaction between pfmdr1 and pfcrt is part of the complex genetic background of CQR.

Rights

Web of Science: "Free full-text from publisher -- gold open access."

Original Publication Citation

Patel, J. J., Thacker, D., Tan, J. C., Pleeter, P., Checkley, L., Gonzales, J. M., . . . Ferdig, M. T. (2010). Chloroquine susceptibility and reversibility in a Plasmodium falciparum genetic cross. Molecular Microbiology, 78(3), 770-787. doi:10.1111/j.1365-2958.2010.07366.x

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