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Plasmodium falciparum genotype and gametocyte prevalence in children with uncomplicated malaria in coastal Ghana
BACKGROUND: Plasmodium falciparum gametocytes are vital to sustaining malaria transmission. Parasite densities, multiplicity of infection as well as asexual genotype are features that have been found to influence gametocyte production. Measurements of the prevalence of Plasmodium sp. gametocytes may...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5148883/ https://www.ncbi.nlm.nih.gov/pubmed/27938356 http://dx.doi.org/10.1186/s12936-016-1640-8 |
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author | Ayanful-Torgby, Ruth Oppong, Akua Abankwa, Joana Acquah, Festus Williamson, Kimberly C. Amoah, Linda Eva |
author_facet | Ayanful-Torgby, Ruth Oppong, Akua Abankwa, Joana Acquah, Festus Williamson, Kimberly C. Amoah, Linda Eva |
author_sort | Ayanful-Torgby, Ruth |
collection | PubMed |
description | BACKGROUND: Plasmodium falciparum gametocytes are vital to sustaining malaria transmission. Parasite densities, multiplicity of infection as well as asexual genotype are features that have been found to influence gametocyte production. Measurements of the prevalence of Plasmodium sp. gametocytes may serve as a tool to monitor the success of malaria eradication efforts. METHODS: Whole blood was collected from 112 children aged between 6 months and 13 years with uncomplicated P. falciparum malaria attending three health facilities in southern Ghana from June to August, 2014 before (day 0) and 4 days after completion of anti-malaria drug treatment (day 7). Malaria parasites were observed by microscopy and polymerase chain reaction (PCR); submicroscopic gametocyte carriage was measured by a Pfs25 (PF3D7_1031000) mRNA real time reverse transcriptase polymerase chain reaction (RT-PCR). Parasite genotyping was performed on gDNA extracted from dried filter paper blood blots by amplification of the polymorphic regions of msp1 (PF3D7_0930300) and msp2 (PF3D7_0206800) using PCR. RESULTS: Microscopy estimated 3.1% (3/96) of the total population to carry gametocytes on day 0, which decreased to 2.1% (2/96) on day 7. In contrast, reverse transcriptase-real time PCR (RT-PCR) analysis of a subset of 35 samples estimated submicroscopic gametocyte carriage to be as high as 77% (27/35) using primers specific for Pfs25 (CT < 35) on day 0 and by day 7 this only declined to 60% (21/35). Genotyping the msp2 gene identified higher levels of MOI than the msp1 gene. CONCLUSIONS: Although below detection by microscopy, gametocyte prevalence at submicroscopic levels are high in this region and emphasize the need for more effective elimination approaches like the development of transmission-blocking vaccines and safer gametocytocidal drugs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12936-016-1640-8) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5148883 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-51488832016-12-16 Plasmodium falciparum genotype and gametocyte prevalence in children with uncomplicated malaria in coastal Ghana Ayanful-Torgby, Ruth Oppong, Akua Abankwa, Joana Acquah, Festus Williamson, Kimberly C. Amoah, Linda Eva Malar J Research BACKGROUND: Plasmodium falciparum gametocytes are vital to sustaining malaria transmission. Parasite densities, multiplicity of infection as well as asexual genotype are features that have been found to influence gametocyte production. Measurements of the prevalence of Plasmodium sp. gametocytes may serve as a tool to monitor the success of malaria eradication efforts. METHODS: Whole blood was collected from 112 children aged between 6 months and 13 years with uncomplicated P. falciparum malaria attending three health facilities in southern Ghana from June to August, 2014 before (day 0) and 4 days after completion of anti-malaria drug treatment (day 7). Malaria parasites were observed by microscopy and polymerase chain reaction (PCR); submicroscopic gametocyte carriage was measured by a Pfs25 (PF3D7_1031000) mRNA real time reverse transcriptase polymerase chain reaction (RT-PCR). Parasite genotyping was performed on gDNA extracted from dried filter paper blood blots by amplification of the polymorphic regions of msp1 (PF3D7_0930300) and msp2 (PF3D7_0206800) using PCR. RESULTS: Microscopy estimated 3.1% (3/96) of the total population to carry gametocytes on day 0, which decreased to 2.1% (2/96) on day 7. In contrast, reverse transcriptase-real time PCR (RT-PCR) analysis of a subset of 35 samples estimated submicroscopic gametocyte carriage to be as high as 77% (27/35) using primers specific for Pfs25 (CT < 35) on day 0 and by day 7 this only declined to 60% (21/35). Genotyping the msp2 gene identified higher levels of MOI than the msp1 gene. CONCLUSIONS: Although below detection by microscopy, gametocyte prevalence at submicroscopic levels are high in this region and emphasize the need for more effective elimination approaches like the development of transmission-blocking vaccines and safer gametocytocidal drugs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12936-016-1640-8) contains supplementary material, which is available to authorized users. BioMed Central 2016-12-09 /pmc/articles/PMC5148883/ /pubmed/27938356 http://dx.doi.org/10.1186/s12936-016-1640-8 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Ayanful-Torgby, Ruth Oppong, Akua Abankwa, Joana Acquah, Festus Williamson, Kimberly C. Amoah, Linda Eva Plasmodium falciparum genotype and gametocyte prevalence in children with uncomplicated malaria in coastal Ghana |
title | Plasmodium falciparum genotype and gametocyte prevalence in children with uncomplicated malaria in coastal Ghana |
title_full | Plasmodium falciparum genotype and gametocyte prevalence in children with uncomplicated malaria in coastal Ghana |
title_fullStr | Plasmodium falciparum genotype and gametocyte prevalence in children with uncomplicated malaria in coastal Ghana |
title_full_unstemmed | Plasmodium falciparum genotype and gametocyte prevalence in children with uncomplicated malaria in coastal Ghana |
title_short | Plasmodium falciparum genotype and gametocyte prevalence in children with uncomplicated malaria in coastal Ghana |
title_sort | plasmodium falciparum genotype and gametocyte prevalence in children with uncomplicated malaria in coastal ghana |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5148883/ https://www.ncbi.nlm.nih.gov/pubmed/27938356 http://dx.doi.org/10.1186/s12936-016-1640-8 |
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