Advances in understanding the genetic basis of antimalarial drug resistance.

Abstract:

:The acquisition of drug resistance by Plasmodium falciparum has severely curtailed global efforts to control malaria. Our ability to define resistance has been greatly enhanced by recent advances in Plasmodium genetics and genomics. Sequencing and microarray studies have identified thousands of polymorphisms in the P. falciparum genome, and linkage disequilibrium analyses have exploited these to rapidly identify known and novel loci that influence parasite susceptibility to antimalarials such as chloroquine, quinine, and sulfadoxine-pyrimethamine. Genetic approaches have also been designed to predict determinants of in vivo resistance to more recent first-line antimalarials such as the artemisinins. Transfection methodologies have defined the role of determinants including pfcrt, pfmdr1, and dhfr. This knowledge can be leveraged to develop more efficient methods of surveillance and treatment.

journal_name

Curr Opin Microbiol

authors

Ekland EH,Fidock DA

doi

10.1016/j.mib.2007.07.007

subject

Has Abstract

pub_date

2007-08-01 00:00:00

pages

363-70

issue

4

eissn

1369-5274

issn

1879-0364

pii

S1369-5274(07)00097-5

journal_volume

10

pub_type

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