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Absence of Putative Artemisinin Resistance Mutations Among Plasmodium falciparum in Sub-Saharan Africa: A Molecular Epidemiologic Study.

  • Steve M. Taylor
  • , Christian M. Parobek
  • , Derrick K. De Conti
  • , Kassoum Kayentao
  • , Sheick Oumar Coulibaly
  • , Brian M. Greenwood
  • , Harry Tagbor
  • , John Williams
  • , Kalifa Bojang
  • , Fanta Njie
  • , Meghna Desai
  • , Simon Kariuki
  • , Julie Gutman
  • , Don P. Mathanga
  • , Andreas Mårtensson
  • , Billy Ngasala
  • , Melissa D. Conrad
  • , Philip J. Rosenthal
  • , Antoinette K. Tshefu
  • , Ann M. Moormann
  • John M. Vulule, Ogobara K. Doumbo, Feiko Ter Kuile, Steven R. Meshnick, Jeffrey A. Bailey, Jonathan J. Juliano
  • Division of Infectious Diseases
  • Duke University
  • University of North Carolina at Chapel Hill
  • University of Massachusetts Medical School
  • Université des Sciences, des Techniques et des Technologies de Bamako
  • Liverpool School of Tropical Medicine
  • Université de Ouagadougou
  • London School of Hygiene and Tropical Medicine
  • Kwame Nkrumah University of Science and Technology
  • University for Development Studies Ghana
  • Medical Research Council Laboratories Gambia
  • Centers for Disease Control and Prevention
  • CDC Kenya
  • Kenya Medical Research Institute Kisumu, Entomology
  • University of Malawi
  • Malaria Research
  • Karolinska Institutet
  • Muhimbili University of Health and Allied Sciences
  • University of California at San Francisco
  • Université de Kinshasa
  • Kenya Medical Research Institute

Research output: Contribution to journalArticlepeer-review

221 Citations (Scopus)

Abstract

Plasmodium falciparum parasites that are resistant to artemisinins have been detected in Southeast Asia. Resistance is associated with several polymorphisms in the parasite's K13-propeller gene. The molecular epidemiology of these artemisinin resistance genotypes in African parasite populations is unknown. We developed an assay to quantify rare polymorphisms in parasite populations that uses a pooled deep-sequencing approach to score allele frequencies, validated it by evaluating mixtures of laboratory parasite strains, and then used it to screen P. falciparum parasites from >1100 African infections collected since 2002 from 14 sites across sub-Saharan Africa. We found no mutations in African parasite populations that are associated with artemisinin resistance in Southeast Asian parasites. However, we observed 15 coding mutations, including 12 novel mutations, and limited allele sharing between parasite populations, consistent with a large reservoir of naturally occurring K13-propeller variation. Although polymorphisms associated with artemisinin resistance in P. falciparum in Southeast Asia are not prevalent in sub-Saharan Africa, numerous K13-propeller coding polymorphisms circulate in Africa. Although their distributions do not support a widespread selective sweep for an artemisinin-resistant phenotype, the impact of these mutations on artemisinin susceptibility is unknown and will require further characterization. Rapid, scalable molecular surveillance offers a useful adjunct in tracking and containing artemisinin resistance.

Original languageEnglish
Pages (from-to)680-688
Number of pages9
JournalJournal of Infectious Diseases
Volume211
Issue number5
DOIs
Publication statusPublished - 1 Sept 2014

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Artemisinin resistance
  • Drug resistance
  • Falciparum malaria
  • Molecular epidemiology

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