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High-resolution micro-epidemiology of parasite spatial and temporal dynamics in a high malaria transmission setting in Kenya

Novel interventions that leverage the heterogeneity of parasite transmission are needed to achieve malaria elimination. To better understand spatial and temporal dynamics of transmission, we applied amplicon next-generation sequencing of two polymorphic gene regions (csp and ama1) to a cohort identi...

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Autores principales: Nelson, Cody S., Sumner, Kelsey M., Freedman, Elizabeth, Saelens, Joseph W., Obala, Andrew A., Mangeni, Judith N., Taylor, Steve M., O’Meara, Wendy P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6901486/
https://www.ncbi.nlm.nih.gov/pubmed/31819062
http://dx.doi.org/10.1038/s41467-019-13578-4
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author Nelson, Cody S.
Sumner, Kelsey M.
Freedman, Elizabeth
Saelens, Joseph W.
Obala, Andrew A.
Mangeni, Judith N.
Taylor, Steve M.
O’Meara, Wendy P.
author_facet Nelson, Cody S.
Sumner, Kelsey M.
Freedman, Elizabeth
Saelens, Joseph W.
Obala, Andrew A.
Mangeni, Judith N.
Taylor, Steve M.
O’Meara, Wendy P.
author_sort Nelson, Cody S.
collection PubMed
description Novel interventions that leverage the heterogeneity of parasite transmission are needed to achieve malaria elimination. To better understand spatial and temporal dynamics of transmission, we applied amplicon next-generation sequencing of two polymorphic gene regions (csp and ama1) to a cohort identified via reactive case detection in a high-transmission setting in western Kenya. From April 2013 to July 2014, we enrolled 442 symptomatic children with malaria, 442 matched controls, and all household members of both groups. Here, we evaluate genetic similarity between infected individuals using three indices: sharing of parasite haplotypes on binary and proportional scales and the L1 norm. Symptomatic children more commonly share haplotypes with their own household members. Furthermore, we observe robust temporal structuring of parasite genetic similarity and identify the unique molecular signature of an outbreak. These findings of both micro- and macro-scale organization of parasite populations might be harnessed to inform next-generation malaria control measures.
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spelling pubmed-69014862019-12-11 High-resolution micro-epidemiology of parasite spatial and temporal dynamics in a high malaria transmission setting in Kenya Nelson, Cody S. Sumner, Kelsey M. Freedman, Elizabeth Saelens, Joseph W. Obala, Andrew A. Mangeni, Judith N. Taylor, Steve M. O’Meara, Wendy P. Nat Commun Article Novel interventions that leverage the heterogeneity of parasite transmission are needed to achieve malaria elimination. To better understand spatial and temporal dynamics of transmission, we applied amplicon next-generation sequencing of two polymorphic gene regions (csp and ama1) to a cohort identified via reactive case detection in a high-transmission setting in western Kenya. From April 2013 to July 2014, we enrolled 442 symptomatic children with malaria, 442 matched controls, and all household members of both groups. Here, we evaluate genetic similarity between infected individuals using three indices: sharing of parasite haplotypes on binary and proportional scales and the L1 norm. Symptomatic children more commonly share haplotypes with their own household members. Furthermore, we observe robust temporal structuring of parasite genetic similarity and identify the unique molecular signature of an outbreak. These findings of both micro- and macro-scale organization of parasite populations might be harnessed to inform next-generation malaria control measures. Nature Publishing Group UK 2019-12-09 /pmc/articles/PMC6901486/ /pubmed/31819062 http://dx.doi.org/10.1038/s41467-019-13578-4 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Nelson, Cody S.
Sumner, Kelsey M.
Freedman, Elizabeth
Saelens, Joseph W.
Obala, Andrew A.
Mangeni, Judith N.
Taylor, Steve M.
O’Meara, Wendy P.
High-resolution micro-epidemiology of parasite spatial and temporal dynamics in a high malaria transmission setting in Kenya
title High-resolution micro-epidemiology of parasite spatial and temporal dynamics in a high malaria transmission setting in Kenya
title_full High-resolution micro-epidemiology of parasite spatial and temporal dynamics in a high malaria transmission setting in Kenya
title_fullStr High-resolution micro-epidemiology of parasite spatial and temporal dynamics in a high malaria transmission setting in Kenya
title_full_unstemmed High-resolution micro-epidemiology of parasite spatial and temporal dynamics in a high malaria transmission setting in Kenya
title_short High-resolution micro-epidemiology of parasite spatial and temporal dynamics in a high malaria transmission setting in Kenya
title_sort high-resolution micro-epidemiology of parasite spatial and temporal dynamics in a high malaria transmission setting in kenya
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6901486/
https://www.ncbi.nlm.nih.gov/pubmed/31819062
http://dx.doi.org/10.1038/s41467-019-13578-4
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