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Hidden paths to endless forms most wonderful: ecology latently shapes evolution of multicellular development in predatory bacteria

Ecological causes of developmental evolution, for example from predation, remain much investigated, but the potential importance of latent phenotypes in eco-evo-devo has received little attention. Using the predatory bacterium Myxococcus xanthus, which undergoes aggregative fruiting body development...

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Autores principales: La Fortezza, Marco, Rendueles, Olaya, Keller, Heike, Velicer, Gregory J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9481553/
https://www.ncbi.nlm.nih.gov/pubmed/36114258
http://dx.doi.org/10.1038/s42003-022-03912-w
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author La Fortezza, Marco
Rendueles, Olaya
Keller, Heike
Velicer, Gregory J.
author_facet La Fortezza, Marco
Rendueles, Olaya
Keller, Heike
Velicer, Gregory J.
author_sort La Fortezza, Marco
collection PubMed
description Ecological causes of developmental evolution, for example from predation, remain much investigated, but the potential importance of latent phenotypes in eco-evo-devo has received little attention. Using the predatory bacterium Myxococcus xanthus, which undergoes aggregative fruiting body development upon starvation, we tested whether adaptation to distinct growth environments that do not induce development latently alters developmental phenotypes under starvation conditions that do induce development. In an evolution experiment named MyxoEE-3, growing M. xanthus populations swarmed across agar surfaces while adapting to conditions varying at factors such as surface stiffness or prey identity. Such ecological variation during growth was found to greatly impact the latent evolution of development, including fruiting body morphology, the degree of morphological trait correlation, reaction norms, degrees of developmental plasticity and stochastic diversification. For example, some prey environments promoted retention of developmental proficiency whereas others led to its systematic loss. Our results have implications for understanding evolutionary interactions among predation, development and motility in myxobacterial life cycles, and, more broadly, how ecology can profoundly shape the evolution of developmental systems latently rather than by direct selection on developmental features.
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spelling pubmed-94815532022-09-18 Hidden paths to endless forms most wonderful: ecology latently shapes evolution of multicellular development in predatory bacteria La Fortezza, Marco Rendueles, Olaya Keller, Heike Velicer, Gregory J. Commun Biol Article Ecological causes of developmental evolution, for example from predation, remain much investigated, but the potential importance of latent phenotypes in eco-evo-devo has received little attention. Using the predatory bacterium Myxococcus xanthus, which undergoes aggregative fruiting body development upon starvation, we tested whether adaptation to distinct growth environments that do not induce development latently alters developmental phenotypes under starvation conditions that do induce development. In an evolution experiment named MyxoEE-3, growing M. xanthus populations swarmed across agar surfaces while adapting to conditions varying at factors such as surface stiffness or prey identity. Such ecological variation during growth was found to greatly impact the latent evolution of development, including fruiting body morphology, the degree of morphological trait correlation, reaction norms, degrees of developmental plasticity and stochastic diversification. For example, some prey environments promoted retention of developmental proficiency whereas others led to its systematic loss. Our results have implications for understanding evolutionary interactions among predation, development and motility in myxobacterial life cycles, and, more broadly, how ecology can profoundly shape the evolution of developmental systems latently rather than by direct selection on developmental features. Nature Publishing Group UK 2022-09-16 /pmc/articles/PMC9481553/ /pubmed/36114258 http://dx.doi.org/10.1038/s42003-022-03912-w Text en © The Author(s) 2022, corrected publication 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
La Fortezza, Marco
Rendueles, Olaya
Keller, Heike
Velicer, Gregory J.
Hidden paths to endless forms most wonderful: ecology latently shapes evolution of multicellular development in predatory bacteria
title Hidden paths to endless forms most wonderful: ecology latently shapes evolution of multicellular development in predatory bacteria
title_full Hidden paths to endless forms most wonderful: ecology latently shapes evolution of multicellular development in predatory bacteria
title_fullStr Hidden paths to endless forms most wonderful: ecology latently shapes evolution of multicellular development in predatory bacteria
title_full_unstemmed Hidden paths to endless forms most wonderful: ecology latently shapes evolution of multicellular development in predatory bacteria
title_short Hidden paths to endless forms most wonderful: ecology latently shapes evolution of multicellular development in predatory bacteria
title_sort hidden paths to endless forms most wonderful: ecology latently shapes evolution of multicellular development in predatory bacteria
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9481553/
https://www.ncbi.nlm.nih.gov/pubmed/36114258
http://dx.doi.org/10.1038/s42003-022-03912-w
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