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Endosymbiotic calcifying bacteria across sponge species and oceans
From an evolutionary point of view, sponges are ideal targets to study marine symbioses as they are the most ancient living metazoans and harbour highly diverse microbial communities. A recently discovered association between the sponge Hemimycale columella and an intracellular bacterium that genera...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5337934/ https://www.ncbi.nlm.nih.gov/pubmed/28262822 http://dx.doi.org/10.1038/srep43674 |
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author | Garate, Leire Sureda, Jan Agell, Gemma Uriz, Maria J. |
author_facet | Garate, Leire Sureda, Jan Agell, Gemma Uriz, Maria J. |
author_sort | Garate, Leire |
collection | PubMed |
description | From an evolutionary point of view, sponges are ideal targets to study marine symbioses as they are the most ancient living metazoans and harbour highly diverse microbial communities. A recently discovered association between the sponge Hemimycale columella and an intracellular bacterium that generates large amounts of calcite spherules has prompted speculation on the possible role of intracellular bacteria in the evolution of the skeleton in early animals. To gain insight into this purportedly ancestral symbiosis, we investigated the presence of symbiotic bacteria in Mediterranean and Caribbean sponges. We found four new calcibacteria OTUs belonging to the SAR116 in two orders (Poecilosclerida and Clionaida) and three families of Demospongiae, two additional OTUs in cnidarians and one more in seawater (at 98.5% similarity). Using a calcibacteria targeted probe and CARD-FISH, we also found calcibacteria in Spirophorida and Suberitida and proved that the calcifying bacteria accumulated at the sponge periphery, forming a skeletal cortex, analogous to that of siliceous microscleres in other demosponges. Bacteria-mediated skeletonization is spread in a range of phylogenetically distant species and thus the purported implication of bacteria in skeleton formation and evolution of early animals gains relevance. |
format | Online Article Text |
id | pubmed-5337934 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53379342017-03-08 Endosymbiotic calcifying bacteria across sponge species and oceans Garate, Leire Sureda, Jan Agell, Gemma Uriz, Maria J. Sci Rep Article From an evolutionary point of view, sponges are ideal targets to study marine symbioses as they are the most ancient living metazoans and harbour highly diverse microbial communities. A recently discovered association between the sponge Hemimycale columella and an intracellular bacterium that generates large amounts of calcite spherules has prompted speculation on the possible role of intracellular bacteria in the evolution of the skeleton in early animals. To gain insight into this purportedly ancestral symbiosis, we investigated the presence of symbiotic bacteria in Mediterranean and Caribbean sponges. We found four new calcibacteria OTUs belonging to the SAR116 in two orders (Poecilosclerida and Clionaida) and three families of Demospongiae, two additional OTUs in cnidarians and one more in seawater (at 98.5% similarity). Using a calcibacteria targeted probe and CARD-FISH, we also found calcibacteria in Spirophorida and Suberitida and proved that the calcifying bacteria accumulated at the sponge periphery, forming a skeletal cortex, analogous to that of siliceous microscleres in other demosponges. Bacteria-mediated skeletonization is spread in a range of phylogenetically distant species and thus the purported implication of bacteria in skeleton formation and evolution of early animals gains relevance. Nature Publishing Group 2017-03-06 /pmc/articles/PMC5337934/ /pubmed/28262822 http://dx.doi.org/10.1038/srep43674 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Garate, Leire Sureda, Jan Agell, Gemma Uriz, Maria J. Endosymbiotic calcifying bacteria across sponge species and oceans |
title | Endosymbiotic calcifying bacteria across sponge species and oceans |
title_full | Endosymbiotic calcifying bacteria across sponge species and oceans |
title_fullStr | Endosymbiotic calcifying bacteria across sponge species and oceans |
title_full_unstemmed | Endosymbiotic calcifying bacteria across sponge species and oceans |
title_short | Endosymbiotic calcifying bacteria across sponge species and oceans |
title_sort | endosymbiotic calcifying bacteria across sponge species and oceans |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5337934/ https://www.ncbi.nlm.nih.gov/pubmed/28262822 http://dx.doi.org/10.1038/srep43674 |
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