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Evolving generalists in switching rugged landscapes
Evolving systems, be it an antibody repertoire in the face of mutating pathogens or a microbial population exposed to varied antibiotics, constantly search for adaptive solutions in time-varying fitness landscapes. Generalists refer to genotypes that remain fit across diverse selective pressures; wh...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6771975/ https://www.ncbi.nlm.nih.gov/pubmed/31574088 http://dx.doi.org/10.1371/journal.pcbi.1007320 |
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author | Wang, Shenshen Dai, Lei |
author_facet | Wang, Shenshen Dai, Lei |
author_sort | Wang, Shenshen |
collection | PubMed |
description | Evolving systems, be it an antibody repertoire in the face of mutating pathogens or a microbial population exposed to varied antibiotics, constantly search for adaptive solutions in time-varying fitness landscapes. Generalists refer to genotypes that remain fit across diverse selective pressures; while multi-drug resistant microbes are undesired yet prevalent, broadly-neutralizing antibodies are much wanted but rare. However, little is known about under what conditions such generalists with a high capacity to adapt can be efficiently discovered by evolution. In addition, can epistasis—the source of landscape ruggedness and path constraints—play a different role, if the environment varies in a non-random way? We present a generative model to estimate the propensity of evolving generalists in rugged landscapes that are tunably related and alternating relatively slowly. We find that environmental cycling can substantially facilitate the search for fit generalists by dynamically enlarging their effective basins of attraction. Importantly, these high performers are most likely to emerge at intermediate levels of ruggedness and environmental relatedness. Our approach allows one to estimate correlations across environments from the topography of experimental fitness landscapes. Our work provides a conceptual framework to study evolution in time-correlated complex environments, and offers statistical understanding that suggests general strategies for eliciting broadly neutralizing antibodies or preventing microbes from evolving multi-drug resistance. |
format | Online Article Text |
id | pubmed-6771975 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-67719752019-10-12 Evolving generalists in switching rugged landscapes Wang, Shenshen Dai, Lei PLoS Comput Biol Research Article Evolving systems, be it an antibody repertoire in the face of mutating pathogens or a microbial population exposed to varied antibiotics, constantly search for adaptive solutions in time-varying fitness landscapes. Generalists refer to genotypes that remain fit across diverse selective pressures; while multi-drug resistant microbes are undesired yet prevalent, broadly-neutralizing antibodies are much wanted but rare. However, little is known about under what conditions such generalists with a high capacity to adapt can be efficiently discovered by evolution. In addition, can epistasis—the source of landscape ruggedness and path constraints—play a different role, if the environment varies in a non-random way? We present a generative model to estimate the propensity of evolving generalists in rugged landscapes that are tunably related and alternating relatively slowly. We find that environmental cycling can substantially facilitate the search for fit generalists by dynamically enlarging their effective basins of attraction. Importantly, these high performers are most likely to emerge at intermediate levels of ruggedness and environmental relatedness. Our approach allows one to estimate correlations across environments from the topography of experimental fitness landscapes. Our work provides a conceptual framework to study evolution in time-correlated complex environments, and offers statistical understanding that suggests general strategies for eliciting broadly neutralizing antibodies or preventing microbes from evolving multi-drug resistance. Public Library of Science 2019-10-01 /pmc/articles/PMC6771975/ /pubmed/31574088 http://dx.doi.org/10.1371/journal.pcbi.1007320 Text en © 2019 Wang, Dai 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 use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Wang, Shenshen Dai, Lei Evolving generalists in switching rugged landscapes |
title | Evolving generalists in switching rugged landscapes |
title_full | Evolving generalists in switching rugged landscapes |
title_fullStr | Evolving generalists in switching rugged landscapes |
title_full_unstemmed | Evolving generalists in switching rugged landscapes |
title_short | Evolving generalists in switching rugged landscapes |
title_sort | evolving generalists in switching rugged landscapes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6771975/ https://www.ncbi.nlm.nih.gov/pubmed/31574088 http://dx.doi.org/10.1371/journal.pcbi.1007320 |
work_keys_str_mv | AT wangshenshen evolvinggeneralistsinswitchingruggedlandscapes AT dailei evolvinggeneralistsinswitchingruggedlandscapes |