Multi-population genomic analysis of malaria parasites indicates local selection and differentiation at the gdv1 locus regulating sexual development
Abstract 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 c...
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oai:doaj.org-article:5832f85adf7a48e2933c54d172a4d56c2021-12-02T15:08:49ZMulti-population genomic analysis of malaria parasites indicates local selection and differentiation at the gdv1 locus regulating sexual development10.1038/s41598-018-34078-32045-2322https://doaj.org/article/5832f85adf7a48e2933c54d172a4d56c2018-10-01T00:00:00Zhttps://doi.org/10.1038/s41598-018-34078-3https://doaj.org/toc/2045-2322Abstract 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.Craig W. DuffyAlfred Amambua-NgwaAmbroise D. AhouidiMahamadou DiakiteGordon A. AwandareHampate BaSarah J. TarrLee MurrayLindsay B. StewartUmberto D’AlessandroThomas D. OttoDominic P. KwiatkowskiDavid J. ConwayNature PortfolioarticleGametocytesFalciparumGambiaeLong-read Sequencing DataRecent Directional SelectionMedicineRScienceQENScientific Reports, Vol 8, Iss 1, Pp 1-12 (2018) |
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Gametocytes Falciparum Gambiae Long-read Sequencing Data Recent Directional Selection Medicine R Science Q |
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Gametocytes Falciparum Gambiae Long-read Sequencing Data Recent Directional Selection Medicine R Science Q Craig W. Duffy Alfred Amambua-Ngwa Ambroise D. Ahouidi Mahamadou Diakite Gordon A. Awandare Hampate Ba Sarah J. Tarr Lee Murray Lindsay B. Stewart Umberto D’Alessandro Thomas D. Otto Dominic P. Kwiatkowski David J. Conway Multi-population genomic analysis of malaria parasites indicates local selection and differentiation at the gdv1 locus regulating sexual development |
description |
Abstract 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 |
article |
author |
Craig W. Duffy Alfred Amambua-Ngwa Ambroise D. Ahouidi Mahamadou Diakite Gordon A. Awandare Hampate Ba Sarah J. Tarr Lee Murray Lindsay B. Stewart Umberto D’Alessandro Thomas D. Otto Dominic P. Kwiatkowski David J. Conway |
author_facet |
Craig W. Duffy Alfred Amambua-Ngwa Ambroise D. Ahouidi Mahamadou Diakite Gordon A. Awandare Hampate Ba Sarah J. Tarr Lee Murray Lindsay B. Stewart Umberto D’Alessandro Thomas D. Otto Dominic P. Kwiatkowski David J. Conway |
author_sort |
Craig W. Duffy |
title |
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_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_sort |
multi-population genomic analysis of malaria parasites indicates local selection and differentiation at the gdv1 locus regulating sexual development |
publisher |
Nature Portfolio |
publishDate |
2018 |
url |
https://doaj.org/article/5832f85adf7a48e2933c54d172a4d56c |
work_keys_str_mv |
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