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Independent Origin of Plasmodium falciparum Antifolate Super-Resistance, Uganda, Tanzania, and Ethiopia
Super-resistant Plasmodium falciparum threatens the effectiveness of sulfadoxine–pyrimethamine in intermittent preventive treatment for malaria during pregnancy. It is characterized by the A581G Pfdhps mutation on a background of the double-mutant Pfdhps and the triple-mutant Pfdhfr. Using samples c...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Centers for Disease Control and Prevention
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4111169/ https://www.ncbi.nlm.nih.gov/pubmed/25061906 http://dx.doi.org/10.3201/eid2008.131897 |
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author | Alifrangis, Michael Nag, Sidsel Schousboe, Mette L. Ishengoma, Deus Lusingu, John Pota, Hirva Kavishe, Reginald A. Pearce, Richard Ord, Rosalynn Lynch, Caroline Dejene, Seyoum Cox, Jonathan Rwakimari, John Minja, Daniel T.R. Lemnge, Martha M. Roper, Cally |
author_facet | Alifrangis, Michael Nag, Sidsel Schousboe, Mette L. Ishengoma, Deus Lusingu, John Pota, Hirva Kavishe, Reginald A. Pearce, Richard Ord, Rosalynn Lynch, Caroline Dejene, Seyoum Cox, Jonathan Rwakimari, John Minja, Daniel T.R. Lemnge, Martha M. Roper, Cally |
author_sort | Alifrangis, Michael |
collection | PubMed |
description | Super-resistant Plasmodium falciparum threatens the effectiveness of sulfadoxine–pyrimethamine in intermittent preventive treatment for malaria during pregnancy. It is characterized by the A581G Pfdhps mutation on a background of the double-mutant Pfdhps and the triple-mutant Pfdhfr. Using samples collected during 2004–2008, we investigated the evolutionary origin of the A581G mutation by characterizing microsatellite diversity flanking Pfdhps triple-mutant (437G+540E+581G) alleles from 3 locations in eastern Africa and comparing it with double-mutant (437G+540E) alleles from the same area. In Ethiopia, both alleles derived from 1 lineage that was distinct from those in Uganda and Tanzania. Uganda and Tanzania triple mutants derived from the previously characterized southeastern Africa double-mutant lineage. The A581G mutation has occurred multiple times on local Pfdhps double-mutant backgrounds; however, a novel microsatellite allele incorporated into the Tanzania lineage since 2004 illustrates the local expansion of emergent triple-mutant lineages. |
format | Online Article Text |
id | pubmed-4111169 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Centers for Disease Control and Prevention |
record_format | MEDLINE/PubMed |
spelling | pubmed-41111692014-08-05 Independent Origin of Plasmodium falciparum Antifolate Super-Resistance, Uganda, Tanzania, and Ethiopia Alifrangis, Michael Nag, Sidsel Schousboe, Mette L. Ishengoma, Deus Lusingu, John Pota, Hirva Kavishe, Reginald A. Pearce, Richard Ord, Rosalynn Lynch, Caroline Dejene, Seyoum Cox, Jonathan Rwakimari, John Minja, Daniel T.R. Lemnge, Martha M. Roper, Cally Emerg Infect Dis Research Super-resistant Plasmodium falciparum threatens the effectiveness of sulfadoxine–pyrimethamine in intermittent preventive treatment for malaria during pregnancy. It is characterized by the A581G Pfdhps mutation on a background of the double-mutant Pfdhps and the triple-mutant Pfdhfr. Using samples collected during 2004–2008, we investigated the evolutionary origin of the A581G mutation by characterizing microsatellite diversity flanking Pfdhps triple-mutant (437G+540E+581G) alleles from 3 locations in eastern Africa and comparing it with double-mutant (437G+540E) alleles from the same area. In Ethiopia, both alleles derived from 1 lineage that was distinct from those in Uganda and Tanzania. Uganda and Tanzania triple mutants derived from the previously characterized southeastern Africa double-mutant lineage. The A581G mutation has occurred multiple times on local Pfdhps double-mutant backgrounds; however, a novel microsatellite allele incorporated into the Tanzania lineage since 2004 illustrates the local expansion of emergent triple-mutant lineages. Centers for Disease Control and Prevention 2014-08 /pmc/articles/PMC4111169/ /pubmed/25061906 http://dx.doi.org/10.3201/eid2008.131897 Text en https://creativecommons.org/licenses/by/4.0/This is a publication of the U.S. Government. This publication is in the public domain and is therefore without copyright. All text from this work may be reprinted freely. Use of these materials should be properly cited. |
spellingShingle | Research Alifrangis, Michael Nag, Sidsel Schousboe, Mette L. Ishengoma, Deus Lusingu, John Pota, Hirva Kavishe, Reginald A. Pearce, Richard Ord, Rosalynn Lynch, Caroline Dejene, Seyoum Cox, Jonathan Rwakimari, John Minja, Daniel T.R. Lemnge, Martha M. Roper, Cally Independent Origin of Plasmodium falciparum Antifolate Super-Resistance, Uganda, Tanzania, and Ethiopia |
title | Independent Origin of Plasmodium falciparum Antifolate Super-Resistance, Uganda, Tanzania, and Ethiopia |
title_full | Independent Origin of Plasmodium falciparum Antifolate Super-Resistance, Uganda, Tanzania, and Ethiopia |
title_fullStr | Independent Origin of Plasmodium falciparum Antifolate Super-Resistance, Uganda, Tanzania, and Ethiopia |
title_full_unstemmed | Independent Origin of Plasmodium falciparum Antifolate Super-Resistance, Uganda, Tanzania, and Ethiopia |
title_short | Independent Origin of Plasmodium falciparum Antifolate Super-Resistance, Uganda, Tanzania, and Ethiopia |
title_sort | independent origin of plasmodium falciparum antifolate super-resistance, uganda, tanzania, and ethiopia |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4111169/ https://www.ncbi.nlm.nih.gov/pubmed/25061906 http://dx.doi.org/10.3201/eid2008.131897 |
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