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Hidden paths to endless forms most wonderful: Complexity of bacterial motility shapes diversification of latent phenotypes

BACKGROUND: Evolution in one selective environment often latently generates phenotypic change that is manifested only later in different environments, but the complexity of behavior important to fitness in the original environment might influence the character of such latent-phenotype evolution. Usi...

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Autores principales: Rendueles, Olaya, Velicer, Gregory J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7641858/
https://www.ncbi.nlm.nih.gov/pubmed/33148179
http://dx.doi.org/10.1186/s12862-020-01707-3
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author Rendueles, Olaya
Velicer, Gregory J.
author_facet Rendueles, Olaya
Velicer, Gregory J.
author_sort Rendueles, Olaya
collection PubMed
description BACKGROUND: Evolution in one selective environment often latently generates phenotypic change that is manifested only later in different environments, but the complexity of behavior important to fitness in the original environment might influence the character of such latent-phenotype evolution. Using Myxococcus xanthus, a bacterium possessing two motility systems differing in effectiveness on hard vs. soft surfaces, we test (i) whether and how evolution while swarming on one surface—the selective surface—latently alters motility on the alternative surface type and (ii) whether patterns of such latent-phenotype evolution depend on the complexity of ancestral motility, specific ancestral motility genotypes and/or the selective surface of evolution. We analysze an experiment in which populations established from three ancestral genotypes—one with both motility systems intact and two others with one system debilitated—evolved while swarming across either hard or soft agar in six evolutionary treatments. We then compare motility-phenotype patterns across selective vs. alternative surface types. RESULTS: Latent motility evolution was pervasive but varied in character as a function of the presence of one or two functional motility systems and, for some individual-treatment comparisons, the specific ancestral genotype and/or selective surface. Swarming rates on alternative vs. selective surfaces were positively correlated generally among populations with one functional motility system but not among those with two. This suggests that opportunities for pleiotropy and epistasis generated by increased genetic complexity underlying behavior can alter the character of latent-phenotype evolution. No tradeoff between motility performance across surface types was detected in the dual-system treatments, even after adaptation on a surface on which one motility system dominates strongly over the other in driving movement, but latent-phenotype evolution was instead idiosyncratic in these treatments. We further find that the magnitude of stochastic diversification at alternative-surface swarming among replicate populations greatly exceeded diversification of selective-surface swarming within some treatments and varied across treatments. CONCLUSION: Collectively, our results suggest that increases in the genetic and mechanistic complexity of behavior can increase the complexity of latent-phenotype evolution outcomes and illustrate that diversification manifested during evolution in one environment can be augmented greatly by diversification of latent phenotypes manifested later.
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spelling pubmed-76418582020-11-05 Hidden paths to endless forms most wonderful: Complexity of bacterial motility shapes diversification of latent phenotypes Rendueles, Olaya Velicer, Gregory J. BMC Evol Biol Research Article BACKGROUND: Evolution in one selective environment often latently generates phenotypic change that is manifested only later in different environments, but the complexity of behavior important to fitness in the original environment might influence the character of such latent-phenotype evolution. Using Myxococcus xanthus, a bacterium possessing two motility systems differing in effectiveness on hard vs. soft surfaces, we test (i) whether and how evolution while swarming on one surface—the selective surface—latently alters motility on the alternative surface type and (ii) whether patterns of such latent-phenotype evolution depend on the complexity of ancestral motility, specific ancestral motility genotypes and/or the selective surface of evolution. We analysze an experiment in which populations established from three ancestral genotypes—one with both motility systems intact and two others with one system debilitated—evolved while swarming across either hard or soft agar in six evolutionary treatments. We then compare motility-phenotype patterns across selective vs. alternative surface types. RESULTS: Latent motility evolution was pervasive but varied in character as a function of the presence of one or two functional motility systems and, for some individual-treatment comparisons, the specific ancestral genotype and/or selective surface. Swarming rates on alternative vs. selective surfaces were positively correlated generally among populations with one functional motility system but not among those with two. This suggests that opportunities for pleiotropy and epistasis generated by increased genetic complexity underlying behavior can alter the character of latent-phenotype evolution. No tradeoff between motility performance across surface types was detected in the dual-system treatments, even after adaptation on a surface on which one motility system dominates strongly over the other in driving movement, but latent-phenotype evolution was instead idiosyncratic in these treatments. We further find that the magnitude of stochastic diversification at alternative-surface swarming among replicate populations greatly exceeded diversification of selective-surface swarming within some treatments and varied across treatments. CONCLUSION: Collectively, our results suggest that increases in the genetic and mechanistic complexity of behavior can increase the complexity of latent-phenotype evolution outcomes and illustrate that diversification manifested during evolution in one environment can be augmented greatly by diversification of latent phenotypes manifested later. BioMed Central 2020-11-04 /pmc/articles/PMC7641858/ /pubmed/33148179 http://dx.doi.org/10.1186/s12862-020-01707-3 Text en © The Author(s) 2020 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/. The Creative Commons Public Domain Dedication waiver (http://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 Article
Rendueles, Olaya
Velicer, Gregory J.
Hidden paths to endless forms most wonderful: Complexity of bacterial motility shapes diversification of latent phenotypes
title Hidden paths to endless forms most wonderful: Complexity of bacterial motility shapes diversification of latent phenotypes
title_full Hidden paths to endless forms most wonderful: Complexity of bacterial motility shapes diversification of latent phenotypes
title_fullStr Hidden paths to endless forms most wonderful: Complexity of bacterial motility shapes diversification of latent phenotypes
title_full_unstemmed Hidden paths to endless forms most wonderful: Complexity of bacterial motility shapes diversification of latent phenotypes
title_short Hidden paths to endless forms most wonderful: Complexity of bacterial motility shapes diversification of latent phenotypes
title_sort hidden paths to endless forms most wonderful: complexity of bacterial motility shapes diversification of latent phenotypes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7641858/
https://www.ncbi.nlm.nih.gov/pubmed/33148179
http://dx.doi.org/10.1186/s12862-020-01707-3
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