Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Dolan, Patrick T, Taguwa, Shuhei, Rangel, Mauricio Aguilar, Acevedo, Ashley, Hagai, Tzachi, Andino, Raul, Frydman, Judith
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
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
_version_ 1783650747670331392
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
work_keys_str_mv AT dolanpatrickt principlesofdenguevirusevolvabilityderivedfromgenotypefitnessmapsinhumanandmosquitocells
AT taguwashuhei principlesofdenguevirusevolvabilityderivedfromgenotypefitnessmapsinhumanandmosquitocells
AT rangelmauricioaguilar principlesofdenguevirusevolvabilityderivedfromgenotypefitnessmapsinhumanandmosquitocells
AT acevedoashley principlesofdenguevirusevolvabilityderivedfromgenotypefitnessmapsinhumanandmosquitocells
AT hagaitzachi principlesofdenguevirusevolvabilityderivedfromgenotypefitnessmapsinhumanandmosquitocells
AT andinoraul principlesofdenguevirusevolvabilityderivedfromgenotypefitnessmapsinhumanandmosquitocells
AT frydmanjudith principlesofdenguevirusevolvabilityderivedfromgenotypefitnessmapsinhumanandmosquitocells