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Long-distance transmission patterns modelled from SNP barcodes of Plasmodium falciparum infections in The Gambia

Malaria has declined significantly in The Gambia and determining transmission dynamics of Plasmodium falciparum can help targeting control interventions towards elimination. This can be inferred from genetic similarity between parasite isolates from different sites and timepoints. Here, we imposed a...

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Autores principales: Amambua-Ngwa, Alfred, Jeffries, David, Mwesigwa, Julia, Seedy-Jawara, Aminata, Okebe, Joseph, Achan, Jane, Drakeley, Chris, Volkman, Sarah, D’Alessandro, Umberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6751170/
https://www.ncbi.nlm.nih.gov/pubmed/31534181
http://dx.doi.org/10.1038/s41598-019-49991-4
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author Amambua-Ngwa, Alfred
Jeffries, David
Mwesigwa, Julia
Seedy-Jawara, Aminata
Okebe, Joseph
Achan, Jane
Drakeley, Chris
Volkman, Sarah
D’Alessandro, Umberto
author_facet Amambua-Ngwa, Alfred
Jeffries, David
Mwesigwa, Julia
Seedy-Jawara, Aminata
Okebe, Joseph
Achan, Jane
Drakeley, Chris
Volkman, Sarah
D’Alessandro, Umberto
author_sort Amambua-Ngwa, Alfred
collection PubMed
description Malaria has declined significantly in The Gambia and determining transmission dynamics of Plasmodium falciparum can help targeting control interventions towards elimination. This can be inferred from genetic similarity between parasite isolates from different sites and timepoints. Here, we imposed a P. falciparum life cycle time on a genetic distance likelihood model to determine transmission paths from a 54 SNP barcode of 355 isolates. Samples were collected monthly during the 2013 malaria season from six pairs of villages spanning 300 km from western to eastern Gambia. There was spatial and temporal hierarchy in pairwise genetic relatedness, with the most similar barcodes from isolates within the same households and village. Constrained by travel data, the model detected 60 directional transmission events, with 27% paths linking persons from different regions. We identified 13 infected individuals (4.2% of those genotyped) responsible for 2 to 8 subsequent infections within their communities. These super-infectors were mostly from high transmission villages. When considering paths between isolates from the most distant regions (west vs east) and travel history, there were 3 transmission paths from eastern to western Gambia, all at the peak (October) of the malaria transmission season. No paths with known travel originated from the extreme west to east. Although more than half of all paths were within-village, parasite flow from east to west may contribute to maintain transmission in western Gambia, where malaria transmission is already low. Therefore, interrupting malaria transmission in western Gambia would require targeting eastern Gambia, where malaria prevalence is substantially higher, with intensified malaria interventions.
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spelling pubmed-67511702019-09-30 Long-distance transmission patterns modelled from SNP barcodes of Plasmodium falciparum infections in The Gambia Amambua-Ngwa, Alfred Jeffries, David Mwesigwa, Julia Seedy-Jawara, Aminata Okebe, Joseph Achan, Jane Drakeley, Chris Volkman, Sarah D’Alessandro, Umberto Sci Rep Article Malaria has declined significantly in The Gambia and determining transmission dynamics of Plasmodium falciparum can help targeting control interventions towards elimination. This can be inferred from genetic similarity between parasite isolates from different sites and timepoints. Here, we imposed a P. falciparum life cycle time on a genetic distance likelihood model to determine transmission paths from a 54 SNP barcode of 355 isolates. Samples were collected monthly during the 2013 malaria season from six pairs of villages spanning 300 km from western to eastern Gambia. There was spatial and temporal hierarchy in pairwise genetic relatedness, with the most similar barcodes from isolates within the same households and village. Constrained by travel data, the model detected 60 directional transmission events, with 27% paths linking persons from different regions. We identified 13 infected individuals (4.2% of those genotyped) responsible for 2 to 8 subsequent infections within their communities. These super-infectors were mostly from high transmission villages. When considering paths between isolates from the most distant regions (west vs east) and travel history, there were 3 transmission paths from eastern to western Gambia, all at the peak (October) of the malaria transmission season. No paths with known travel originated from the extreme west to east. Although more than half of all paths were within-village, parasite flow from east to west may contribute to maintain transmission in western Gambia, where malaria transmission is already low. Therefore, interrupting malaria transmission in western Gambia would require targeting eastern Gambia, where malaria prevalence is substantially higher, with intensified malaria interventions. Nature Publishing Group UK 2019-09-18 /pmc/articles/PMC6751170/ /pubmed/31534181 http://dx.doi.org/10.1038/s41598-019-49991-4 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
Amambua-Ngwa, Alfred
Jeffries, David
Mwesigwa, Julia
Seedy-Jawara, Aminata
Okebe, Joseph
Achan, Jane
Drakeley, Chris
Volkman, Sarah
D’Alessandro, Umberto
Long-distance transmission patterns modelled from SNP barcodes of Plasmodium falciparum infections in The Gambia
title Long-distance transmission patterns modelled from SNP barcodes of Plasmodium falciparum infections in The Gambia
title_full Long-distance transmission patterns modelled from SNP barcodes of Plasmodium falciparum infections in The Gambia
title_fullStr Long-distance transmission patterns modelled from SNP barcodes of Plasmodium falciparum infections in The Gambia
title_full_unstemmed Long-distance transmission patterns modelled from SNP barcodes of Plasmodium falciparum infections in The Gambia
title_short Long-distance transmission patterns modelled from SNP barcodes of Plasmodium falciparum infections in The Gambia
title_sort long-distance transmission patterns modelled from snp barcodes of plasmodium falciparum infections in the gambia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6751170/
https://www.ncbi.nlm.nih.gov/pubmed/31534181
http://dx.doi.org/10.1038/s41598-019-49991-4
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