Genetics of Mefloquine Resistance in the Rodent Malaria Parasite Plasmodium chabaudi

Author:

Cravo Pedro V. L.12,Carlton Jane M.-R.3,Hunt Paul1,Bisoni Laura4,Padua Rose Ann5,Walliker David1

Affiliation:

1. Institute of Cell, Animal, and Population Biology, University of Edinburgh, Edinburgh EH9 3JT

2. Centro de Malária e Outras Doenças Tropicais/IHMT, 1349-008 Lisbon, Portugal

3. The Institute for Genomic Research, Rockville, Maryland 20850

4. Wellcome Trust Centre for Cell Biology, University of Edinburgh, Edinburgh EH9 3JR, Scotland

5. Department of Haematological Medicine, King's College Hospital, London SE5 9NU, United Kingdom

Abstract

ABSTRACT The genetic determinants of resistance to mefloquine in malaria parasites are unclear. Some studies have implied that amplification of, or mutations in, the multidrug resistance gene pfmdr1 in Plasmodium falciparum may be involved. Using the rodent malaria model Plasmodium chabaudi , we investigated the role of the orthologue of this gene, pcmdr1 , in a stable mefloquine-resistant mutant, AS(15MF/3), selected from a sensitive clone. pcmdr1 exists as a single copy gene on chromosome 12 of the sensitive clone. In AS(15MF/3), the gene was found to have undergone duplication, with one copy translocating to chromosome 4. mRNA levels of pcmdr1 were higher in the mutant than in the parent sensitive clone. A partial genetic map of the translocation showed that other genes in addition to pcmdr1 had been cotranslocated. The sequences of both copies of pcmdr1 of AS(15MF/3) were identical to that of the parent sensitive clone. A cross was made between AS(15MF/3) and an unrelated mefloquine-sensitive clone, AJ. Phenotypic and molecular analysis of progeny clones showed that duplication and overexpression of the pcmdr1 gene was an important determinant of resistance. However, not all mefloquine-resistant progeny contained the duplicated gene, showing that at least one other gene was involved in resistance.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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