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Multi-population genomic analysis of malaria parasites indicates local selection and differentiation at the gdv1 locus regulating sexual development
Parasites infect hosts in widely varying environments, encountering diverse challenges for adaptation. To identify malaria parasite genes under locally divergent selection across a large endemic region with a wide spectrum of transmission intensity, genome sequences were obtained from 284 clinical P...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6202401/ https://www.ncbi.nlm.nih.gov/pubmed/30361631 http://dx.doi.org/10.1038/s41598-018-34078-3 |
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author | Duffy, Craig W. Amambua-Ngwa, Alfred Ahouidi, Ambroise D. Diakite, Mahamadou Awandare, Gordon A. Ba, Hampate Tarr, Sarah J. Murray, Lee Stewart, Lindsay B. D’Alessandro, Umberto Otto, Thomas D. Kwiatkowski, Dominic P. Conway, David J. |
author_facet | Duffy, Craig W. Amambua-Ngwa, Alfred Ahouidi, Ambroise D. Diakite, Mahamadou Awandare, Gordon A. Ba, Hampate Tarr, Sarah J. Murray, Lee Stewart, Lindsay B. D’Alessandro, Umberto Otto, Thomas D. Kwiatkowski, Dominic P. Conway, David J. |
author_sort | Duffy, Craig W. |
collection | PubMed |
description | Parasites infect hosts in widely varying environments, encountering diverse challenges for adaptation. To identify malaria parasite genes under locally divergent selection across a large endemic region with a wide spectrum of transmission intensity, genome sequences were obtained from 284 clinical Plasmodium falciparum infections from four newly sampled locations in Senegal, The Gambia, Mali and Guinea. Combining these with previous data from seven other sites in West Africa enabled a multi-population analysis to identify discrete loci under varying local selection. A genome-wide scan showed the most exceptional geographical divergence to be at the early gametocyte gene locus gdv1 which is essential for parasite sexual development and transmission. We identified a major structural dimorphism with alternative 1.5 kb and 1.0 kb sequence deletions at different positions of the 3′-intergenic region, in tight linkage disequilibrium with the most highly differentiated single nucleotide polymorphism, one of the alleles being very frequent in Senegal and The Gambia but rare in the other locations. Long non-coding RNA transcripts were previously shown to include the entire antisense of the gdv1 coding sequence and the portion of the intergenic region with allelic deletions, suggesting adaptive regulation of parasite sexual development and transmission in response to local conditions. |
format | Online Article Text |
id | pubmed-6202401 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62024012018-10-29 Multi-population genomic analysis of malaria parasites indicates local selection and differentiation at the gdv1 locus regulating sexual development Duffy, Craig W. Amambua-Ngwa, Alfred Ahouidi, Ambroise D. Diakite, Mahamadou Awandare, Gordon A. Ba, Hampate Tarr, Sarah J. Murray, Lee Stewart, Lindsay B. D’Alessandro, Umberto Otto, Thomas D. Kwiatkowski, Dominic P. Conway, David J. Sci Rep Article Parasites infect hosts in widely varying environments, encountering diverse challenges for adaptation. To identify malaria parasite genes under locally divergent selection across a large endemic region with a wide spectrum of transmission intensity, genome sequences were obtained from 284 clinical Plasmodium falciparum infections from four newly sampled locations in Senegal, The Gambia, Mali and Guinea. Combining these with previous data from seven other sites in West Africa enabled a multi-population analysis to identify discrete loci under varying local selection. A genome-wide scan showed the most exceptional geographical divergence to be at the early gametocyte gene locus gdv1 which is essential for parasite sexual development and transmission. We identified a major structural dimorphism with alternative 1.5 kb and 1.0 kb sequence deletions at different positions of the 3′-intergenic region, in tight linkage disequilibrium with the most highly differentiated single nucleotide polymorphism, one of the alleles being very frequent in Senegal and The Gambia but rare in the other locations. Long non-coding RNA transcripts were previously shown to include the entire antisense of the gdv1 coding sequence and the portion of the intergenic region with allelic deletions, suggesting adaptive regulation of parasite sexual development and transmission in response to local conditions. Nature Publishing Group UK 2018-10-25 /pmc/articles/PMC6202401/ /pubmed/30361631 http://dx.doi.org/10.1038/s41598-018-34078-3 Text en © The Author(s) 2018 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 Duffy, Craig W. Amambua-Ngwa, Alfred Ahouidi, Ambroise D. Diakite, Mahamadou Awandare, Gordon A. Ba, Hampate Tarr, Sarah J. Murray, Lee Stewart, Lindsay B. D’Alessandro, Umberto Otto, Thomas D. Kwiatkowski, Dominic P. Conway, David J. Multi-population genomic analysis of malaria parasites indicates local selection and differentiation at the gdv1 locus regulating sexual development |
title | Multi-population genomic analysis of malaria parasites indicates local selection and differentiation at the gdv1 locus regulating sexual development |
title_full | Multi-population genomic analysis of malaria parasites indicates local selection and differentiation at the gdv1 locus regulating sexual development |
title_fullStr | Multi-population genomic analysis of malaria parasites indicates local selection and differentiation at the gdv1 locus regulating sexual development |
title_full_unstemmed | Multi-population genomic analysis of malaria parasites indicates local selection and differentiation at the gdv1 locus regulating sexual development |
title_short | Multi-population genomic analysis of malaria parasites indicates local selection and differentiation at the gdv1 locus regulating sexual development |
title_sort | multi-population genomic analysis of malaria parasites indicates local selection and differentiation at the gdv1 locus regulating sexual development |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6202401/ https://www.ncbi.nlm.nih.gov/pubmed/30361631 http://dx.doi.org/10.1038/s41598-018-34078-3 |
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