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A cohort study of Plasmodium falciparum infection dynamics in Western Kenya Highlands

BACKGROUND: The Kenyan highlands were malaria-free before the 1910s, but a series of malaria epidemics have occurred in the highlands of western Kenya since the 1980s. Longitudinal studies of the genetic structure, complexity, infection dynamics, and duration of naturally acquired Plasmodium falcipa...

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Autores principales: Baliraine, Frederick N, Afrane, Yaw A, Amenya, Dolphine A, Bonizzoni, Mariangela, Vardo-Zalik, Anne M, Menge, David M, Githeko, Andrew K, Yan, Guiyun
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2955685/
https://www.ncbi.nlm.nih.gov/pubmed/20868504
http://dx.doi.org/10.1186/1471-2334-10-283
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author Baliraine, Frederick N
Afrane, Yaw A
Amenya, Dolphine A
Bonizzoni, Mariangela
Vardo-Zalik, Anne M
Menge, David M
Githeko, Andrew K
Yan, Guiyun
author_facet Baliraine, Frederick N
Afrane, Yaw A
Amenya, Dolphine A
Bonizzoni, Mariangela
Vardo-Zalik, Anne M
Menge, David M
Githeko, Andrew K
Yan, Guiyun
author_sort Baliraine, Frederick N
collection PubMed
description BACKGROUND: The Kenyan highlands were malaria-free before the 1910s, but a series of malaria epidemics have occurred in the highlands of western Kenya since the 1980s. Longitudinal studies of the genetic structure, complexity, infection dynamics, and duration of naturally acquired Plasmodium falciparum infections are needed to facilitate a comprehensive understanding of malaria epidemiology in the complex Kenyan highland eco-epidemiological systems where malaria recently expanded, as well as the evaluation of control measures. METHODS: We followed a cohort of 246 children residing in 3 villages at altitudes 1430 - 1580 m in western Kenya. Monthly parasitological surveys were undertaken for one year, yielding 866 P. falciparum isolates that were analyzed using 10 microsatellite markers. RESULTS: Infection complexity and genetic diversity were high (H(E )= 0.787-0.816), with ≥83% of infections harboring more than one parasite clone. Diversity remained high even during the low malaria transmission season. There was no significant difference between levels of genetic diversity and population structure between high and low transmission seasons. Infection turn-over rate was high, with the average infection duration of single parasite genotypes being 1.11 months, and the longest genotype persistence was 3 months. CONCLUSIONS: These data demonstrate that despite the relatively recent spread of malaria to the highlands, parasite populations seem to have stabilized with no evidence of bottlenecks between seasons, while the ability of residents to clear or control infections indicates presence of effective anti-plasmodial immune mechanisms.
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spelling pubmed-29556852010-10-16 A cohort study of Plasmodium falciparum infection dynamics in Western Kenya Highlands Baliraine, Frederick N Afrane, Yaw A Amenya, Dolphine A Bonizzoni, Mariangela Vardo-Zalik, Anne M Menge, David M Githeko, Andrew K Yan, Guiyun BMC Infect Dis Research Article BACKGROUND: The Kenyan highlands were malaria-free before the 1910s, but a series of malaria epidemics have occurred in the highlands of western Kenya since the 1980s. Longitudinal studies of the genetic structure, complexity, infection dynamics, and duration of naturally acquired Plasmodium falciparum infections are needed to facilitate a comprehensive understanding of malaria epidemiology in the complex Kenyan highland eco-epidemiological systems where malaria recently expanded, as well as the evaluation of control measures. METHODS: We followed a cohort of 246 children residing in 3 villages at altitudes 1430 - 1580 m in western Kenya. Monthly parasitological surveys were undertaken for one year, yielding 866 P. falciparum isolates that were analyzed using 10 microsatellite markers. RESULTS: Infection complexity and genetic diversity were high (H(E )= 0.787-0.816), with ≥83% of infections harboring more than one parasite clone. Diversity remained high even during the low malaria transmission season. There was no significant difference between levels of genetic diversity and population structure between high and low transmission seasons. Infection turn-over rate was high, with the average infection duration of single parasite genotypes being 1.11 months, and the longest genotype persistence was 3 months. CONCLUSIONS: These data demonstrate that despite the relatively recent spread of malaria to the highlands, parasite populations seem to have stabilized with no evidence of bottlenecks between seasons, while the ability of residents to clear or control infections indicates presence of effective anti-plasmodial immune mechanisms. BioMed Central 2010-09-24 /pmc/articles/PMC2955685/ /pubmed/20868504 http://dx.doi.org/10.1186/1471-2334-10-283 Text en Copyright ©2010 Baliraine et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Baliraine, Frederick N
Afrane, Yaw A
Amenya, Dolphine A
Bonizzoni, Mariangela
Vardo-Zalik, Anne M
Menge, David M
Githeko, Andrew K
Yan, Guiyun
A cohort study of Plasmodium falciparum infection dynamics in Western Kenya Highlands
title A cohort study of Plasmodium falciparum infection dynamics in Western Kenya Highlands
title_full A cohort study of Plasmodium falciparum infection dynamics in Western Kenya Highlands
title_fullStr A cohort study of Plasmodium falciparum infection dynamics in Western Kenya Highlands
title_full_unstemmed A cohort study of Plasmodium falciparum infection dynamics in Western Kenya Highlands
title_short A cohort study of Plasmodium falciparum infection dynamics in Western Kenya Highlands
title_sort cohort study of plasmodium falciparum infection dynamics in western kenya highlands
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2955685/
https://www.ncbi.nlm.nih.gov/pubmed/20868504
http://dx.doi.org/10.1186/1471-2334-10-283
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