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Evolution of transcriptional control of antigenic variation and virulence in human and ape malaria parasites
BACKGROUND: The most severe form of human malaria is caused by the protozoan parasite Plasmodium falciparum. This unicellular organism is a member of a subgenus of Plasmodium called the Laverania that infects apes, with P. falciparum being the only member that infects humans. The exceptional virulen...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8265125/ https://www.ncbi.nlm.nih.gov/pubmed/34238209 http://dx.doi.org/10.1186/s12862-021-01872-z |
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author | Gross, Mackensie R. Hsu, Rosie Deitsch, Kirk W. |
author_facet | Gross, Mackensie R. Hsu, Rosie Deitsch, Kirk W. |
author_sort | Gross, Mackensie R. |
collection | PubMed |
description | BACKGROUND: The most severe form of human malaria is caused by the protozoan parasite Plasmodium falciparum. This unicellular organism is a member of a subgenus of Plasmodium called the Laverania that infects apes, with P. falciparum being the only member that infects humans. The exceptional virulence of this species to humans can be largely attributed to a family of variant surface antigens placed by the parasites onto the surface of infected red blood cells that mediate adherence to the vascular endothelium. These proteins are encoded by a large, multicopy gene family called var, with each var gene encoding a different form of the protein. By changing which var gene is expressed, parasites avoid immune recognition, a process called antigenic variation that underlies the chronic nature of malaria infections. RESULTS: Here we show that the common ancestor of the branch of the Laverania lineage that includes the human parasite underwent a remarkable change in the organization and structure of elements linked to the complex transcriptional regulation displayed by the var gene family. Unlike the other members of the Laverania, the clade that gave rise to P. falciparum evolved distinct subsets of var genes distinguishable by different upstream transcriptional regulatory regions that have been associated with different expression profiles and virulence properties. In addition, two uniquely conserved var genes that have been proposed to play a role in coordinating transcriptional switching similarly arose uniquely within this clade. We hypothesize that these changes originated at a time of dramatic climatic change on the African continent that is predicted to have led to significant changes in transmission dynamics, thus selecting for patterns of antigenic variation that enabled lengthier, more chronic infections. CONCLUSIONS: These observations suggest that changes in transmission dynamics selected for significant alterations in the transcriptional regulatory mechanisms that mediate antigenic variation in the parasite lineage that includes P. falciparum. These changes likely underlie the chronic nature of these infections as well as their exceptional virulence. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12862-021-01872-z. |
format | Online Article Text |
id | pubmed-8265125 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-82651252021-07-09 Evolution of transcriptional control of antigenic variation and virulence in human and ape malaria parasites Gross, Mackensie R. Hsu, Rosie Deitsch, Kirk W. BMC Ecol Evol Research BACKGROUND: The most severe form of human malaria is caused by the protozoan parasite Plasmodium falciparum. This unicellular organism is a member of a subgenus of Plasmodium called the Laverania that infects apes, with P. falciparum being the only member that infects humans. The exceptional virulence of this species to humans can be largely attributed to a family of variant surface antigens placed by the parasites onto the surface of infected red blood cells that mediate adherence to the vascular endothelium. These proteins are encoded by a large, multicopy gene family called var, with each var gene encoding a different form of the protein. By changing which var gene is expressed, parasites avoid immune recognition, a process called antigenic variation that underlies the chronic nature of malaria infections. RESULTS: Here we show that the common ancestor of the branch of the Laverania lineage that includes the human parasite underwent a remarkable change in the organization and structure of elements linked to the complex transcriptional regulation displayed by the var gene family. Unlike the other members of the Laverania, the clade that gave rise to P. falciparum evolved distinct subsets of var genes distinguishable by different upstream transcriptional regulatory regions that have been associated with different expression profiles and virulence properties. In addition, two uniquely conserved var genes that have been proposed to play a role in coordinating transcriptional switching similarly arose uniquely within this clade. We hypothesize that these changes originated at a time of dramatic climatic change on the African continent that is predicted to have led to significant changes in transmission dynamics, thus selecting for patterns of antigenic variation that enabled lengthier, more chronic infections. CONCLUSIONS: These observations suggest that changes in transmission dynamics selected for significant alterations in the transcriptional regulatory mechanisms that mediate antigenic variation in the parasite lineage that includes P. falciparum. These changes likely underlie the chronic nature of these infections as well as their exceptional virulence. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12862-021-01872-z. BioMed Central 2021-07-08 /pmc/articles/PMC8265125/ /pubmed/34238209 http://dx.doi.org/10.1186/s12862-021-01872-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Gross, Mackensie R. Hsu, Rosie Deitsch, Kirk W. Evolution of transcriptional control of antigenic variation and virulence in human and ape malaria parasites |
title | Evolution of transcriptional control of antigenic variation and virulence in human and ape malaria parasites |
title_full | Evolution of transcriptional control of antigenic variation and virulence in human and ape malaria parasites |
title_fullStr | Evolution of transcriptional control of antigenic variation and virulence in human and ape malaria parasites |
title_full_unstemmed | Evolution of transcriptional control of antigenic variation and virulence in human and ape malaria parasites |
title_short | Evolution of transcriptional control of antigenic variation and virulence in human and ape malaria parasites |
title_sort | evolution of transcriptional control of antigenic variation and virulence in human and ape malaria parasites |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8265125/ https://www.ncbi.nlm.nih.gov/pubmed/34238209 http://dx.doi.org/10.1186/s12862-021-01872-z |
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