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Modeling the dynamics of Plasmodium falciparum gametocytes in humans during malaria infection
Renewed efforts to eliminate malaria have highlighted the potential to interrupt human-to-mosquito transmission — a process mediated by gametocyte kinetics in human hosts. Here we study the in vivo dynamics of Plasmodium falciparum gametocytes by establishing a framework which incorporates improved...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6819085/ https://www.ncbi.nlm.nih.gov/pubmed/31658944 http://dx.doi.org/10.7554/eLife.49058 |
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author | Cao, Pengxing Collins, Katharine A Zaloumis, Sophie Wattanakul, Thanaporn Tarning, Joel Simpson, Julie A McCarthy, James McCaw, James M |
author_facet | Cao, Pengxing Collins, Katharine A Zaloumis, Sophie Wattanakul, Thanaporn Tarning, Joel Simpson, Julie A McCarthy, James McCaw, James M |
author_sort | Cao, Pengxing |
collection | PubMed |
description | Renewed efforts to eliminate malaria have highlighted the potential to interrupt human-to-mosquito transmission — a process mediated by gametocyte kinetics in human hosts. Here we study the in vivo dynamics of Plasmodium falciparum gametocytes by establishing a framework which incorporates improved measurements of parasitemia, a novel gametocyte dynamics model and model fitting using Bayesian hierarchical inference. We found that the model provides an excellent fit to the clinical data from 17 volunteers infected with P. falciparum (3D7 strain) and reliably predicts observed gametocytemia. We estimated the sexual commitment rate and gametocyte sequestration time to be 0.54% (95% credible interval: 0.30–1.00%) per asexual replication cycle and 8.39 (6.54–10.59) days respectively. We used the data-calibrated model to investigate human-to-mosquito transmissibility, providing a method to link within-human host infection kinetics to epidemiological-scale infection and transmission patterns. |
format | Online Article Text |
id | pubmed-6819085 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-68190852019-10-30 Modeling the dynamics of Plasmodium falciparum gametocytes in humans during malaria infection Cao, Pengxing Collins, Katharine A Zaloumis, Sophie Wattanakul, Thanaporn Tarning, Joel Simpson, Julie A McCarthy, James McCaw, James M eLife Computational and Systems Biology Renewed efforts to eliminate malaria have highlighted the potential to interrupt human-to-mosquito transmission — a process mediated by gametocyte kinetics in human hosts. Here we study the in vivo dynamics of Plasmodium falciparum gametocytes by establishing a framework which incorporates improved measurements of parasitemia, a novel gametocyte dynamics model and model fitting using Bayesian hierarchical inference. We found that the model provides an excellent fit to the clinical data from 17 volunteers infected with P. falciparum (3D7 strain) and reliably predicts observed gametocytemia. We estimated the sexual commitment rate and gametocyte sequestration time to be 0.54% (95% credible interval: 0.30–1.00%) per asexual replication cycle and 8.39 (6.54–10.59) days respectively. We used the data-calibrated model to investigate human-to-mosquito transmissibility, providing a method to link within-human host infection kinetics to epidemiological-scale infection and transmission patterns. eLife Sciences Publications, Ltd 2019-10-29 /pmc/articles/PMC6819085/ /pubmed/31658944 http://dx.doi.org/10.7554/eLife.49058 Text en © 2019, Cao et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Computational and Systems Biology Cao, Pengxing Collins, Katharine A Zaloumis, Sophie Wattanakul, Thanaporn Tarning, Joel Simpson, Julie A McCarthy, James McCaw, James M Modeling the dynamics of Plasmodium falciparum gametocytes in humans during malaria infection |
title | Modeling the dynamics of Plasmodium falciparum gametocytes in humans during malaria infection |
title_full | Modeling the dynamics of Plasmodium falciparum gametocytes in humans during malaria infection |
title_fullStr | Modeling the dynamics of Plasmodium falciparum gametocytes in humans during malaria infection |
title_full_unstemmed | Modeling the dynamics of Plasmodium falciparum gametocytes in humans during malaria infection |
title_short | Modeling the dynamics of Plasmodium falciparum gametocytes in humans during malaria infection |
title_sort | modeling the dynamics of plasmodium falciparum gametocytes in humans during malaria infection |
topic | Computational and Systems Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6819085/ https://www.ncbi.nlm.nih.gov/pubmed/31658944 http://dx.doi.org/10.7554/eLife.49058 |
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