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Ancient Introgression between Two Ape Malaria Parasite Species
The Laverania clade comprises the human malaria parasite Plasmodium falciparum as well as at least seven additional parasite species that infect wild African apes. A recent analysis of Laverania genome sequences (Otto TD, et al. 2018. Genomes of all known members of a Plasmodium subgenus reveal path...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7145702/ https://www.ncbi.nlm.nih.gov/pubmed/31697367 http://dx.doi.org/10.1093/gbe/evz244 |
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author | Plenderleith, Lindsey J Liu, Weimin Learn, Gerald H Loy, Dorothy E Speede, Sheri Sanz, Crickette M Morgan, David B Bertolani, Paco Hart, John A Hart, Terese B Hahn, Beatrice H Sharp, Paul M |
author_facet | Plenderleith, Lindsey J Liu, Weimin Learn, Gerald H Loy, Dorothy E Speede, Sheri Sanz, Crickette M Morgan, David B Bertolani, Paco Hart, John A Hart, Terese B Hahn, Beatrice H Sharp, Paul M |
author_sort | Plenderleith, Lindsey J |
collection | PubMed |
description | The Laverania clade comprises the human malaria parasite Plasmodium falciparum as well as at least seven additional parasite species that infect wild African apes. A recent analysis of Laverania genome sequences (Otto TD, et al. 2018. Genomes of all known members of a Plasmodium subgenus reveal paths to virulent human malaria. Nat Microbiol. 3: 687–697) reported three instances of interspecies gene transfer, one of which had previously been described. Generating gene sequences from additional ape parasites and re-examining sequencing reads generated in the Otto et al. study, we identified one of the newly described gene transfers as an assembly artifact of sequences derived from a sample coinfected by two parasite species. The second gene transfer between ancestors of two divergent chimpanzee parasite lineages was confirmed, but involved a much larger number of genes than originally described, many of which encode exported proteins that remodel, or bind to, erythrocytes. Because successful hybridization between Laverania species is very rare, it will be important to determine to what extent these gene transfers have shaped their host interactions. |
format | Online Article Text |
id | pubmed-7145702 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-71457022020-04-13 Ancient Introgression between Two Ape Malaria Parasite Species Plenderleith, Lindsey J Liu, Weimin Learn, Gerald H Loy, Dorothy E Speede, Sheri Sanz, Crickette M Morgan, David B Bertolani, Paco Hart, John A Hart, Terese B Hahn, Beatrice H Sharp, Paul M Genome Biol Evol Letter The Laverania clade comprises the human malaria parasite Plasmodium falciparum as well as at least seven additional parasite species that infect wild African apes. A recent analysis of Laverania genome sequences (Otto TD, et al. 2018. Genomes of all known members of a Plasmodium subgenus reveal paths to virulent human malaria. Nat Microbiol. 3: 687–697) reported three instances of interspecies gene transfer, one of which had previously been described. Generating gene sequences from additional ape parasites and re-examining sequencing reads generated in the Otto et al. study, we identified one of the newly described gene transfers as an assembly artifact of sequences derived from a sample coinfected by two parasite species. The second gene transfer between ancestors of two divergent chimpanzee parasite lineages was confirmed, but involved a much larger number of genes than originally described, many of which encode exported proteins that remodel, or bind to, erythrocytes. Because successful hybridization between Laverania species is very rare, it will be important to determine to what extent these gene transfers have shaped their host interactions. Oxford University Press 2019-11-07 /pmc/articles/PMC7145702/ /pubmed/31697367 http://dx.doi.org/10.1093/gbe/evz244 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Letter Plenderleith, Lindsey J Liu, Weimin Learn, Gerald H Loy, Dorothy E Speede, Sheri Sanz, Crickette M Morgan, David B Bertolani, Paco Hart, John A Hart, Terese B Hahn, Beatrice H Sharp, Paul M Ancient Introgression between Two Ape Malaria Parasite Species |
title | Ancient Introgression between Two Ape Malaria Parasite Species |
title_full | Ancient Introgression between Two Ape Malaria Parasite Species |
title_fullStr | Ancient Introgression between Two Ape Malaria Parasite Species |
title_full_unstemmed | Ancient Introgression between Two Ape Malaria Parasite Species |
title_short | Ancient Introgression between Two Ape Malaria Parasite Species |
title_sort | ancient introgression between two ape malaria parasite species |
topic | Letter |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7145702/ https://www.ncbi.nlm.nih.gov/pubmed/31697367 http://dx.doi.org/10.1093/gbe/evz244 |
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