4.5 Review

Drug resistance genomics of the antimalarial drug artemisinin

Journal

GENOME BIOLOGY
Volume 15, Issue 11, Pages -

Publisher

BMC
DOI: 10.1186/s13059-014-0544-6

Keywords

-

Funding

  1. NIAID [R01AI103058, R01AI090141]
  2. Bill Melinda Gates Foundation [OPP1040406]
  3. Medicines for Malaria Venture
  4. Hertz Fellowship
  5. UCSD Genetics Training Program through the National Institute of General Medical Sciences [T32 GM008666]
  6. Bill and Melinda Gates Foundation [OPP1040406] Funding Source: Bill and Melinda Gates Foundation

Ask authors/readers for more resources

Across the globe, over 200 million annual malaria infections result in up to 660,000 deaths, 77% of which occur in children under the age of five years. Although prevention is important, malaria deaths are typically prevented by using antimalarial drugs that eliminate symptoms and clear parasites from the blood. Artemisinins are one of the few remaining compound classes that can be used to cure multidrug-resistant Plasmodium falciparum infections. Unfortunately, clinical trials from Southeast Asia are showing that artemisinin-based treatments are beginning to lose their effectiveness, adding renewed urgency to the search for the genetic determinants of parasite resistance to this important drug class. We review the genetic and genomic approaches that have led to an improved understanding of artemisinin resistance, including the identification of resistance-conferring mutations in the P. falciparum kelch13 gene.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available