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Phaeobacter inhibens induces apoptosis-like programmed cell death in calcifying Emiliania huxleyi
The model coccolithophore, Emiliania huxleyi, forms expansive blooms dominated by the calcifying cell type, which produce calcite scales called coccoliths. Blooms last several weeks, after which the calcified algal cells rapidly die, descending into the deep ocean. E. huxleyi bloom collapse is attri...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6426857/ https://www.ncbi.nlm.nih.gov/pubmed/30894549 http://dx.doi.org/10.1038/s41598-018-36847-6 |
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author | Bramucci, Anna R. Case, Rebecca J. |
author_facet | Bramucci, Anna R. Case, Rebecca J. |
author_sort | Bramucci, Anna R. |
collection | PubMed |
description | The model coccolithophore, Emiliania huxleyi, forms expansive blooms dominated by the calcifying cell type, which produce calcite scales called coccoliths. Blooms last several weeks, after which the calcified algal cells rapidly die, descending into the deep ocean. E. huxleyi bloom collapse is attributed to E. huxleyi viruses (EhVs) that infect and kill calcifying cells, while other E. huxleyi pathogens, such as bacteria belonging to the roseobacter clade, are overlooked. EhVs kill calcifying E. huxleyi by inducing production of bioactive viral-glycosphingolipids (vGSLs), which trigger algal programmed cell death (PCD). The roseobacter Phaeobacter inhibens was recently shown to interact with and kill the calcifying cell type of E. huxleyi, but the mechanism of algal death remains unelucidated. Here we demonstrate that P. inhibens kills calcifying E. huxleyi by inducing a highly specific type of PCD called apoptosis-like-PCD (AL-PCD). Host death can successfully be abolished in the presence of a pan-caspase inhibitor, which prevents the activation of caspase-like molecules. This finding differentiates P. inhibens and EhV pathogenesis of E. huxleyi, by demonstrating that bacterial-induced AL-PCD requires active caspase-like molecules, while the viral pathogen does not. This is the first demonstration of a bacterium inducing AL-PCD in an algal host as a killing mechanism. |
format | Online Article Text |
id | pubmed-6426857 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64268572019-03-27 Phaeobacter inhibens induces apoptosis-like programmed cell death in calcifying Emiliania huxleyi Bramucci, Anna R. Case, Rebecca J. Sci Rep Article The model coccolithophore, Emiliania huxleyi, forms expansive blooms dominated by the calcifying cell type, which produce calcite scales called coccoliths. Blooms last several weeks, after which the calcified algal cells rapidly die, descending into the deep ocean. E. huxleyi bloom collapse is attributed to E. huxleyi viruses (EhVs) that infect and kill calcifying cells, while other E. huxleyi pathogens, such as bacteria belonging to the roseobacter clade, are overlooked. EhVs kill calcifying E. huxleyi by inducing production of bioactive viral-glycosphingolipids (vGSLs), which trigger algal programmed cell death (PCD). The roseobacter Phaeobacter inhibens was recently shown to interact with and kill the calcifying cell type of E. huxleyi, but the mechanism of algal death remains unelucidated. Here we demonstrate that P. inhibens kills calcifying E. huxleyi by inducing a highly specific type of PCD called apoptosis-like-PCD (AL-PCD). Host death can successfully be abolished in the presence of a pan-caspase inhibitor, which prevents the activation of caspase-like molecules. This finding differentiates P. inhibens and EhV pathogenesis of E. huxleyi, by demonstrating that bacterial-induced AL-PCD requires active caspase-like molecules, while the viral pathogen does not. This is the first demonstration of a bacterium inducing AL-PCD in an algal host as a killing mechanism. Nature Publishing Group UK 2019-03-21 /pmc/articles/PMC6426857/ /pubmed/30894549 http://dx.doi.org/10.1038/s41598-018-36847-6 Text en © The Author(s) 2019 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/. |
spellingShingle | Article Bramucci, Anna R. Case, Rebecca J. Phaeobacter inhibens induces apoptosis-like programmed cell death in calcifying Emiliania huxleyi |
title | Phaeobacter inhibens induces apoptosis-like programmed cell death in calcifying Emiliania huxleyi |
title_full | Phaeobacter inhibens induces apoptosis-like programmed cell death in calcifying Emiliania huxleyi |
title_fullStr | Phaeobacter inhibens induces apoptosis-like programmed cell death in calcifying Emiliania huxleyi |
title_full_unstemmed | Phaeobacter inhibens induces apoptosis-like programmed cell death in calcifying Emiliania huxleyi |
title_short | Phaeobacter inhibens induces apoptosis-like programmed cell death in calcifying Emiliania huxleyi |
title_sort | phaeobacter inhibens induces apoptosis-like programmed cell death in calcifying emiliania huxleyi |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6426857/ https://www.ncbi.nlm.nih.gov/pubmed/30894549 http://dx.doi.org/10.1038/s41598-018-36847-6 |
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