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A computational lens for sexual-stage transmission, reproduction, fitness and kinetics in Plasmodium falciparum

BACKGROUND: The burden of falciparum malaria remains unacceptably high in much of sub-Saharan Africa and massive efforts are underway to eliminate the parasite. While symptoms of malaria are caused by asexual reproduction of the parasite, transmission to new human hosts relies entirely on male and f...

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Autores principales: Lawniczak, Mara K. N., Eckhoff, Philip A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5031309/
https://www.ncbi.nlm.nih.gov/pubmed/27653663
http://dx.doi.org/10.1186/s12936-016-1538-5
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author Lawniczak, Mara K. N.
Eckhoff, Philip A.
author_facet Lawniczak, Mara K. N.
Eckhoff, Philip A.
author_sort Lawniczak, Mara K. N.
collection PubMed
description BACKGROUND: The burden of falciparum malaria remains unacceptably high in much of sub-Saharan Africa and massive efforts are underway to eliminate the parasite. While symptoms of malaria are caused by asexual reproduction of the parasite, transmission to new human hosts relies entirely on male and female sexual-stage parasites, known as gametocytes. Successful transmission can be observed at very low gametocyte densities, which raises the question of whether transmission-enhancing mechanisms exist in the human host, the mosquito, or both. METHODS: A new computational model was developed to investigate the probability of fertilization over a range of overdispersion parameters and male gamete exploration rates. Simulations were used to fit a likelihood surface for data on rates of mosquito infection across a wide range of host gametocyte densities. RESULTS: The best fit simultaneously requires very strong overdispersion and faster gamete exploration than is possible with random swimming in order to explain typical prevalence levels in mosquitoes. Gametocyte overdispersion or clustering in the human host and faster gamete exploration of the mosquito blood meal are highly probably given these results. CONCLUSIONS: Density-dependent gametocyte clustering in the human host, and non-random searching (e.g., chemotaxis) in the mosquito are probable. Future work should aim to discover these mechanisms, as disrupting parasite development in the mosquito will play a critical role in eliminating malaria. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12936-016-1538-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-50313092016-09-29 A computational lens for sexual-stage transmission, reproduction, fitness and kinetics in Plasmodium falciparum Lawniczak, Mara K. N. Eckhoff, Philip A. Malar J Research BACKGROUND: The burden of falciparum malaria remains unacceptably high in much of sub-Saharan Africa and massive efforts are underway to eliminate the parasite. While symptoms of malaria are caused by asexual reproduction of the parasite, transmission to new human hosts relies entirely on male and female sexual-stage parasites, known as gametocytes. Successful transmission can be observed at very low gametocyte densities, which raises the question of whether transmission-enhancing mechanisms exist in the human host, the mosquito, or both. METHODS: A new computational model was developed to investigate the probability of fertilization over a range of overdispersion parameters and male gamete exploration rates. Simulations were used to fit a likelihood surface for data on rates of mosquito infection across a wide range of host gametocyte densities. RESULTS: The best fit simultaneously requires very strong overdispersion and faster gamete exploration than is possible with random swimming in order to explain typical prevalence levels in mosquitoes. Gametocyte overdispersion or clustering in the human host and faster gamete exploration of the mosquito blood meal are highly probably given these results. CONCLUSIONS: Density-dependent gametocyte clustering in the human host, and non-random searching (e.g., chemotaxis) in the mosquito are probable. Future work should aim to discover these mechanisms, as disrupting parasite development in the mosquito will play a critical role in eliminating malaria. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12936-016-1538-5) contains supplementary material, which is available to authorized users. BioMed Central 2016-09-21 /pmc/articles/PMC5031309/ /pubmed/27653663 http://dx.doi.org/10.1186/s12936-016-1538-5 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
Lawniczak, Mara K. N.
Eckhoff, Philip A.
A computational lens for sexual-stage transmission, reproduction, fitness and kinetics in Plasmodium falciparum
title A computational lens for sexual-stage transmission, reproduction, fitness and kinetics in Plasmodium falciparum
title_full A computational lens for sexual-stage transmission, reproduction, fitness and kinetics in Plasmodium falciparum
title_fullStr A computational lens for sexual-stage transmission, reproduction, fitness and kinetics in Plasmodium falciparum
title_full_unstemmed A computational lens for sexual-stage transmission, reproduction, fitness and kinetics in Plasmodium falciparum
title_short A computational lens for sexual-stage transmission, reproduction, fitness and kinetics in Plasmodium falciparum
title_sort computational lens for sexual-stage transmission, reproduction, fitness and kinetics in plasmodium falciparum
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5031309/
https://www.ncbi.nlm.nih.gov/pubmed/27653663
http://dx.doi.org/10.1186/s12936-016-1538-5
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