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The Malaria TaqMan Array Card Includes 87 Assays for Plasmodium falciparum Drug Resistance, Identification of Species, and Genotyping in a Single Reaction
Antimalarial drug resistance exacerbates the global disease burden and complicates eradication efforts. To facilitate the surveillance of resistance markers in countries of malaria endemicity, we developed a suite of TaqMan assays for known resistance markers and compartmentalized them into a single...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5404514/ https://www.ncbi.nlm.nih.gov/pubmed/28264857 http://dx.doi.org/10.1128/AAC.00110-17 |
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author | Pholwat, Suporn Liu, Jie Stroup, Suzanne Jacob, Shevin T. Banura, Patrick Moore, Christopher C. Huang, Fang Laufer, Miriam K. Houpt, Eric Guler, Jennifer L. |
author_facet | Pholwat, Suporn Liu, Jie Stroup, Suzanne Jacob, Shevin T. Banura, Patrick Moore, Christopher C. Huang, Fang Laufer, Miriam K. Houpt, Eric Guler, Jennifer L. |
author_sort | Pholwat, Suporn |
collection | PubMed |
description | Antimalarial drug resistance exacerbates the global disease burden and complicates eradication efforts. To facilitate the surveillance of resistance markers in countries of malaria endemicity, we developed a suite of TaqMan assays for known resistance markers and compartmentalized them into a single array card (TaqMan array card, TAC). We included 87 assays for species identification, for the detection of Plasmodium falciparum mutations associated with chloroquine, atovaquone, pyrimethamine, sulfadoxine, and artemisinin resistance, and for neutral single nucleotide polymorphism (SNP) genotyping. Assay performance was first optimized using DNA from common laboratory parasite lines and plasmid controls. The limit of detection was 0.1 to 10 pg of DNA and yielded 100% accuracy compared to sequencing. The tool was then evaluated on 87 clinical blood samples from around the world, and the malaria TAC once again achieved 100% accuracy compared to sequencing and in addition detected the presence of mixed infections in clinical samples. With its streamlined protocol and high accuracy, this malaria TAC should be a useful tool for large-scale antimalarial resistance surveillance. |
format | Online Article Text |
id | pubmed-5404514 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-54045142017-05-09 The Malaria TaqMan Array Card Includes 87 Assays for Plasmodium falciparum Drug Resistance, Identification of Species, and Genotyping in a Single Reaction Pholwat, Suporn Liu, Jie Stroup, Suzanne Jacob, Shevin T. Banura, Patrick Moore, Christopher C. Huang, Fang Laufer, Miriam K. Houpt, Eric Guler, Jennifer L. Antimicrob Agents Chemother Epidemiology and Surveillance Antimalarial drug resistance exacerbates the global disease burden and complicates eradication efforts. To facilitate the surveillance of resistance markers in countries of malaria endemicity, we developed a suite of TaqMan assays for known resistance markers and compartmentalized them into a single array card (TaqMan array card, TAC). We included 87 assays for species identification, for the detection of Plasmodium falciparum mutations associated with chloroquine, atovaquone, pyrimethamine, sulfadoxine, and artemisinin resistance, and for neutral single nucleotide polymorphism (SNP) genotyping. Assay performance was first optimized using DNA from common laboratory parasite lines and plasmid controls. The limit of detection was 0.1 to 10 pg of DNA and yielded 100% accuracy compared to sequencing. The tool was then evaluated on 87 clinical blood samples from around the world, and the malaria TAC once again achieved 100% accuracy compared to sequencing and in addition detected the presence of mixed infections in clinical samples. With its streamlined protocol and high accuracy, this malaria TAC should be a useful tool for large-scale antimalarial resistance surveillance. American Society for Microbiology 2017-04-24 /pmc/articles/PMC5404514/ /pubmed/28264857 http://dx.doi.org/10.1128/AAC.00110-17 Text en Copyright © 2017 Pholwat et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Epidemiology and Surveillance Pholwat, Suporn Liu, Jie Stroup, Suzanne Jacob, Shevin T. Banura, Patrick Moore, Christopher C. Huang, Fang Laufer, Miriam K. Houpt, Eric Guler, Jennifer L. The Malaria TaqMan Array Card Includes 87 Assays for Plasmodium falciparum Drug Resistance, Identification of Species, and Genotyping in a Single Reaction |
title | The Malaria TaqMan Array Card Includes 87 Assays for Plasmodium falciparum Drug Resistance, Identification of Species, and Genotyping in a Single Reaction |
title_full | The Malaria TaqMan Array Card Includes 87 Assays for Plasmodium falciparum Drug Resistance, Identification of Species, and Genotyping in a Single Reaction |
title_fullStr | The Malaria TaqMan Array Card Includes 87 Assays for Plasmodium falciparum Drug Resistance, Identification of Species, and Genotyping in a Single Reaction |
title_full_unstemmed | The Malaria TaqMan Array Card Includes 87 Assays for Plasmodium falciparum Drug Resistance, Identification of Species, and Genotyping in a Single Reaction |
title_short | The Malaria TaqMan Array Card Includes 87 Assays for Plasmodium falciparum Drug Resistance, Identification of Species, and Genotyping in a Single Reaction |
title_sort | malaria taqman array card includes 87 assays for plasmodium falciparum drug resistance, identification of species, and genotyping in a single reaction |
topic | Epidemiology and Surveillance |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5404514/ https://www.ncbi.nlm.nih.gov/pubmed/28264857 http://dx.doi.org/10.1128/AAC.00110-17 |
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