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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2023
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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. |
format | Online Article Text |
id | pubmed-10320657 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
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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