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From commensalism to parasitism within a genus-level clade of barnacles

Understanding how animals evolve to become parasites is key to unravelling how biodiversity is generated as a whole, as parasites could account for half of all species richness. Two significant impediments to this are that parasites fossilize poorly and that they retain few clear shared morphologica...

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Autores principales: Watanabe, Hiromi Kayama, Uyeno, Daisuke, Yamamori, Luna, Jimi, Naoto, Chen, Chong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10320657/
https://www.ncbi.nlm.nih.gov/pubmed/37403574
http://dx.doi.org/10.1098/rsbl.2022.0550
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author Watanabe, Hiromi Kayama
Uyeno, Daisuke
Yamamori, Luna
Jimi, Naoto
Chen, Chong
author_facet Watanabe, Hiromi Kayama
Uyeno, Daisuke
Yamamori, Luna
Jimi, Naoto
Chen, Chong
author_sort Watanabe, Hiromi Kayama
collection PubMed
description Understanding how animals evolve to become parasites is key to unravelling how biodiversity is generated as a whole, as parasites could account for half of all species richness. Two significant impediments to this are that parasites fossilize poorly and that they retain few clear shared morphological features with non-parasitic relatives. Barnacles include some of the most astonishingly adapted parasites with the adult body reduced to just a network of tubes plus an external reproductive body, but how they originated from the sessile, filter-feeding form is still a mystery. Here, we present compelling molecular evidence that the exceedingly rare scale-worm parasite barnacle Rhizolepas is positioned within a clade comprising species currently assigned to Octolasmis, a genus exclusively commensal with at least six different phyla of animals. Our results imply that species in this genus-level clade represent an array of species at various transitional stages from free-living to parasitic in terms of plate reduction and host-parasite intimacy. Diverging only about 19.15 million years ago, the route to parasitism in Rhizolepas was associated with rapid modifications in anatomy, a pattern that was likely true for many other parasitic lineages.
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spelling pubmed-103206572023-07-06 From commensalism to parasitism within a genus-level clade of barnacles Watanabe, Hiromi Kayama Uyeno, Daisuke Yamamori, Luna Jimi, Naoto Chen, Chong Biol Lett Evolutionary Biology Understanding how animals evolve to become parasites is key to unravelling how biodiversity is generated as a whole, as parasites could account for half of all species richness. Two significant impediments to this are that parasites fossilize poorly and that they retain few clear shared morphological features with non-parasitic relatives. Barnacles include some of the most astonishingly adapted parasites with the adult body reduced to just a network of tubes plus an external reproductive body, but how they originated from the sessile, filter-feeding form is still a mystery. Here, we present compelling molecular evidence that the exceedingly rare scale-worm parasite barnacle Rhizolepas is positioned within a clade comprising species currently assigned to Octolasmis, a genus exclusively commensal with at least six different phyla of animals. Our results imply that species in this genus-level clade represent an array of species at various transitional stages from free-living to parasitic in terms of plate reduction and host-parasite intimacy. Diverging only about 19.15 million years ago, the route to parasitism in Rhizolepas was associated with rapid modifications in anatomy, a pattern that was likely true for many other parasitic lineages. The Royal Society 2023-07-05 /pmc/articles/PMC10320657/ /pubmed/37403574 http://dx.doi.org/10.1098/rsbl.2022.0550 Text en © 2023 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited.
spellingShingle Evolutionary Biology
Watanabe, Hiromi Kayama
Uyeno, Daisuke
Yamamori, Luna
Jimi, Naoto
Chen, Chong
From commensalism to parasitism within a genus-level clade of barnacles
title From commensalism to parasitism within a genus-level clade of barnacles
title_full From commensalism to parasitism within a genus-level clade of barnacles
title_fullStr From commensalism to parasitism within a genus-level clade of barnacles
title_full_unstemmed From commensalism to parasitism within a genus-level clade of barnacles
title_short From commensalism to parasitism within a genus-level clade of barnacles
title_sort from commensalism to parasitism within a genus-level clade of barnacles
topic Evolutionary Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10320657/
https://www.ncbi.nlm.nih.gov/pubmed/37403574
http://dx.doi.org/10.1098/rsbl.2022.0550
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