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Principles of dengue virus evolvability derived from genotype-fitness maps in human and mosquito cells
Dengue virus (DENV) cycles between mosquito and mammalian hosts. To examine how DENV populations adapt to these different host environments, we used serial passage in human and mosquito cell lines and estimated fitness effects for all single-nucleotide variants in these populations using ultra-deep...
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/PMC7880689/ https://www.ncbi.nlm.nih.gov/pubmed/33491648 http://dx.doi.org/10.7554/eLife.61921 |
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author | Dolan, Patrick T Taguwa, Shuhei Rangel, Mauricio Aguilar Acevedo, Ashley Hagai, Tzachi Andino, Raul Frydman, Judith |
author_facet | Dolan, Patrick T Taguwa, Shuhei Rangel, Mauricio Aguilar Acevedo, Ashley Hagai, Tzachi Andino, Raul Frydman, Judith |
author_sort | Dolan, Patrick T |
collection | PubMed |
description | Dengue virus (DENV) cycles between mosquito and mammalian hosts. To examine how DENV populations adapt to these different host environments, we used serial passage in human and mosquito cell lines and estimated fitness effects for all single-nucleotide variants in these populations using ultra-deep sequencing. This allowed us to determine the contributions of beneficial and deleterious mutations to the collective fitness of the population. Our analysis revealed that the continuous influx of a large burden of deleterious mutations counterbalances the effect of rare, host-specific beneficial mutations to shape the path of adaptation. Beneficial mutations preferentially map to intrinsically disordered domains in the viral proteome and cluster to defined regions in the genome. These phenotypically redundant adaptive alleles may facilitate host-specific DENV adaptation. Importantly, the evolutionary constraints described in our simple system mirror trends observed across DENV and Zika strains, indicating it recapitulates key biophysical and biological constraints shaping long-term viral evolution. |
format | Online Article Text |
id | pubmed-7880689 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-78806892021-02-16 Principles of dengue virus evolvability derived from genotype-fitness maps in human and mosquito cells Dolan, Patrick T Taguwa, Shuhei Rangel, Mauricio Aguilar Acevedo, Ashley Hagai, Tzachi Andino, Raul Frydman, Judith eLife Evolutionary Biology Dengue virus (DENV) cycles between mosquito and mammalian hosts. To examine how DENV populations adapt to these different host environments, we used serial passage in human and mosquito cell lines and estimated fitness effects for all single-nucleotide variants in these populations using ultra-deep sequencing. This allowed us to determine the contributions of beneficial and deleterious mutations to the collective fitness of the population. Our analysis revealed that the continuous influx of a large burden of deleterious mutations counterbalances the effect of rare, host-specific beneficial mutations to shape the path of adaptation. Beneficial mutations preferentially map to intrinsically disordered domains in the viral proteome and cluster to defined regions in the genome. These phenotypically redundant adaptive alleles may facilitate host-specific DENV adaptation. Importantly, the evolutionary constraints described in our simple system mirror trends observed across DENV and Zika strains, indicating it recapitulates key biophysical and biological constraints shaping long-term viral evolution. eLife Sciences Publications, Ltd 2021-01-25 /pmc/articles/PMC7880689/ /pubmed/33491648 http://dx.doi.org/10.7554/eLife.61921 Text en © 2021, Dolan et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Evolutionary Biology Dolan, Patrick T Taguwa, Shuhei Rangel, Mauricio Aguilar Acevedo, Ashley Hagai, Tzachi Andino, Raul Frydman, Judith Principles of dengue virus evolvability derived from genotype-fitness maps in human and mosquito cells |
title | Principles of dengue virus evolvability derived from genotype-fitness maps in human and mosquito cells |
title_full | Principles of dengue virus evolvability derived from genotype-fitness maps in human and mosquito cells |
title_fullStr | Principles of dengue virus evolvability derived from genotype-fitness maps in human and mosquito cells |
title_full_unstemmed | Principles of dengue virus evolvability derived from genotype-fitness maps in human and mosquito cells |
title_short | Principles of dengue virus evolvability derived from genotype-fitness maps in human and mosquito cells |
title_sort | principles of dengue virus evolvability derived from genotype-fitness maps in human and mosquito cells |
topic | Evolutionary Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7880689/ https://www.ncbi.nlm.nih.gov/pubmed/33491648 http://dx.doi.org/10.7554/eLife.61921 |
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