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Common host variation drives malaria parasite fitness in healthy human red cells
The replication of Plasmodium falciparum parasites within red blood cells (RBCs) causes severe disease in humans, especially in Africa. Deleterious alleles like hemoglobin S are well-known to confer strong resistance to malaria, but the effects of common RBC variation are largely undetermined. Here,...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8497061/ https://www.ncbi.nlm.nih.gov/pubmed/34553687 http://dx.doi.org/10.7554/eLife.69808 |
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author | Ebel, Emily R Kuypers, Frans A Lin, Carrie Petrov, Dmitri A Egan, Elizabeth S |
author_facet | Ebel, Emily R Kuypers, Frans A Lin, Carrie Petrov, Dmitri A Egan, Elizabeth S |
author_sort | Ebel, Emily R |
collection | PubMed |
description | The replication of Plasmodium falciparum parasites within red blood cells (RBCs) causes severe disease in humans, especially in Africa. Deleterious alleles like hemoglobin S are well-known to confer strong resistance to malaria, but the effects of common RBC variation are largely undetermined. Here, we collected fresh blood samples from 121 healthy donors, most with African ancestry, and performed exome sequencing, detailed RBC phenotyping, and parasite fitness assays. Over one-third of healthy donors unknowingly carried alleles for G6PD deficiency or hemoglobinopathies, which were associated with characteristic RBC phenotypes. Among non-carriers alone, variation in RBC hydration, membrane deformability, and volume was strongly associated with P. falciparum growth rate. Common genetic variants in PIEZO1, SPTA1/SPTB, and several P. falciparum invasion receptors were also associated with parasite growth rate. Interestingly, we observed little or negative evidence for divergent selection on non-pathogenic RBC variation between Africans and Europeans. These findings suggest a model in which globally widespread variation in a moderate number of genes and phenotypes modulates P. falciparum fitness in RBCs. |
format | Online Article Text |
id | pubmed-8497061 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-84970612021-10-08 Common host variation drives malaria parasite fitness in healthy human red cells Ebel, Emily R Kuypers, Frans A Lin, Carrie Petrov, Dmitri A Egan, Elizabeth S eLife Evolutionary Biology The replication of Plasmodium falciparum parasites within red blood cells (RBCs) causes severe disease in humans, especially in Africa. Deleterious alleles like hemoglobin S are well-known to confer strong resistance to malaria, but the effects of common RBC variation are largely undetermined. Here, we collected fresh blood samples from 121 healthy donors, most with African ancestry, and performed exome sequencing, detailed RBC phenotyping, and parasite fitness assays. Over one-third of healthy donors unknowingly carried alleles for G6PD deficiency or hemoglobinopathies, which were associated with characteristic RBC phenotypes. Among non-carriers alone, variation in RBC hydration, membrane deformability, and volume was strongly associated with P. falciparum growth rate. Common genetic variants in PIEZO1, SPTA1/SPTB, and several P. falciparum invasion receptors were also associated with parasite growth rate. Interestingly, we observed little or negative evidence for divergent selection on non-pathogenic RBC variation between Africans and Europeans. These findings suggest a model in which globally widespread variation in a moderate number of genes and phenotypes modulates P. falciparum fitness in RBCs. eLife Sciences Publications, Ltd 2021-09-23 /pmc/articles/PMC8497061/ /pubmed/34553687 http://dx.doi.org/10.7554/eLife.69808 Text en © 2021, Ebel et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Evolutionary Biology Ebel, Emily R Kuypers, Frans A Lin, Carrie Petrov, Dmitri A Egan, Elizabeth S Common host variation drives malaria parasite fitness in healthy human red cells |
title | Common host variation drives malaria parasite fitness in healthy human red cells |
title_full | Common host variation drives malaria parasite fitness in healthy human red cells |
title_fullStr | Common host variation drives malaria parasite fitness in healthy human red cells |
title_full_unstemmed | Common host variation drives malaria parasite fitness in healthy human red cells |
title_short | Common host variation drives malaria parasite fitness in healthy human red cells |
title_sort | common host variation drives malaria parasite fitness in healthy human red cells |
topic | Evolutionary Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8497061/ https://www.ncbi.nlm.nih.gov/pubmed/34553687 http://dx.doi.org/10.7554/eLife.69808 |
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