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Independent Lineages of Highly Sulfadoxine-Resistant Plasmodium falciparum Haplotypes, Eastern Africa
Sulfadoxine-resistant Plasmodium falciparum undermines malaria prevention with sulfadoxine/pyrimethamine. Parasites with a highly resistant mutant dihydropteroate synthase (dhps) haplotype have recently emerged in eastern Africa; they negated preventive benefits of sulfadoxine/pyrimethamine, and mig...
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/PMC4073871/ https://www.ncbi.nlm.nih.gov/pubmed/24960247 http://dx.doi.org/10.3201/eid2007.131720 |
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author | Taylor, Steve M. Antonia, Alejandro L. Harrington, Whitney E. Goheen, Morgan M. Mwapasa, Victor Chaluluka, Ebbie Fried, Michal Kabyemela, Edward Madanitsa, Mwayi Khairallah, Carole Kalilani-Phiri, Linda Tshefu, Antoinette K. Rogerson, Stephen J. ter Kuile, Feiko O. Duffy, Patrick E. Meshnick, Steven R. |
author_facet | Taylor, Steve M. Antonia, Alejandro L. Harrington, Whitney E. Goheen, Morgan M. Mwapasa, Victor Chaluluka, Ebbie Fried, Michal Kabyemela, Edward Madanitsa, Mwayi Khairallah, Carole Kalilani-Phiri, Linda Tshefu, Antoinette K. Rogerson, Stephen J. ter Kuile, Feiko O. Duffy, Patrick E. Meshnick, Steven R. |
author_sort | Taylor, Steve M. |
collection | PubMed |
description | Sulfadoxine-resistant Plasmodium falciparum undermines malaria prevention with sulfadoxine/pyrimethamine. Parasites with a highly resistant mutant dihydropteroate synthase (dhps) haplotype have recently emerged in eastern Africa; they negated preventive benefits of sulfadoxine/pyrimethamine, and might exacerbate placental malaria. We explored emerging lineages of dhps mutant haplotypes in Malawi, the Democratic Republic of the Congo, and Tanzania by using analyses of genetic microsatellites flanking the dhps locus. In Malawi, a triple-mutant dhps SGEG (mutant amino acids are underlined) haplotype emerged in 2010 that was closely related to pre-existing double-mutant SGEA haplotypes, suggesting local origination in Malawi. When we compared mutant strains with parasites from the Democratic Republic of the Congo and Tanzania by multiple independent analyses, we found that SGEG parasites were partitioned into separate lineages by country. These findings support a model of local origination of SGEG dhps haplotypes, rather than geographic diffusion, and have implications for investigations of emergence and effects of parasite drug resistance. |
format | Online Article Text |
id | pubmed-4073871 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Centers for Disease Control and Prevention |
record_format | MEDLINE/PubMed |
spelling | pubmed-40738712014-07-16 Independent Lineages of Highly Sulfadoxine-Resistant Plasmodium falciparum Haplotypes, Eastern Africa Taylor, Steve M. Antonia, Alejandro L. Harrington, Whitney E. Goheen, Morgan M. Mwapasa, Victor Chaluluka, Ebbie Fried, Michal Kabyemela, Edward Madanitsa, Mwayi Khairallah, Carole Kalilani-Phiri, Linda Tshefu, Antoinette K. Rogerson, Stephen J. ter Kuile, Feiko O. Duffy, Patrick E. Meshnick, Steven R. Emerg Infect Dis Research Sulfadoxine-resistant Plasmodium falciparum undermines malaria prevention with sulfadoxine/pyrimethamine. Parasites with a highly resistant mutant dihydropteroate synthase (dhps) haplotype have recently emerged in eastern Africa; they negated preventive benefits of sulfadoxine/pyrimethamine, and might exacerbate placental malaria. We explored emerging lineages of dhps mutant haplotypes in Malawi, the Democratic Republic of the Congo, and Tanzania by using analyses of genetic microsatellites flanking the dhps locus. In Malawi, a triple-mutant dhps SGEG (mutant amino acids are underlined) haplotype emerged in 2010 that was closely related to pre-existing double-mutant SGEA haplotypes, suggesting local origination in Malawi. When we compared mutant strains with parasites from the Democratic Republic of the Congo and Tanzania by multiple independent analyses, we found that SGEG parasites were partitioned into separate lineages by country. These findings support a model of local origination of SGEG dhps haplotypes, rather than geographic diffusion, and have implications for investigations of emergence and effects of parasite drug resistance. Centers for Disease Control and Prevention 2014-07 /pmc/articles/PMC4073871/ /pubmed/24960247 http://dx.doi.org/10.3201/eid2007.131720 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 Taylor, Steve M. Antonia, Alejandro L. Harrington, Whitney E. Goheen, Morgan M. Mwapasa, Victor Chaluluka, Ebbie Fried, Michal Kabyemela, Edward Madanitsa, Mwayi Khairallah, Carole Kalilani-Phiri, Linda Tshefu, Antoinette K. Rogerson, Stephen J. ter Kuile, Feiko O. Duffy, Patrick E. Meshnick, Steven R. Independent Lineages of Highly Sulfadoxine-Resistant Plasmodium falciparum Haplotypes, Eastern Africa |
title | Independent Lineages of Highly Sulfadoxine-Resistant Plasmodium falciparum Haplotypes, Eastern Africa |
title_full | Independent Lineages of Highly Sulfadoxine-Resistant Plasmodium falciparum Haplotypes, Eastern Africa |
title_fullStr | Independent Lineages of Highly Sulfadoxine-Resistant Plasmodium falciparum Haplotypes, Eastern Africa |
title_full_unstemmed | Independent Lineages of Highly Sulfadoxine-Resistant Plasmodium falciparum Haplotypes, Eastern Africa |
title_short | Independent Lineages of Highly Sulfadoxine-Resistant Plasmodium falciparum Haplotypes, Eastern Africa |
title_sort | independent lineages of highly sulfadoxine-resistant plasmodium falciparum haplotypes, eastern africa |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4073871/ https://www.ncbi.nlm.nih.gov/pubmed/24960247 http://dx.doi.org/10.3201/eid2007.131720 |
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