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Dynamic metabolic exchange governs a marine algal-bacterial interaction

Emiliania huxleyi is a model coccolithophore micro-alga that generates vast blooms in the ocean. Bacteria are not considered among the major factors influencing coccolithophore physiology. Here we show through a laboratory model system that the bacterium Phaeobacter inhibens, a well-studied member o...

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Autores principales: Segev, Einat, Wyche, Thomas P, Kim, Ki Hyun, Petersen, Jörn, Ellebrandt, Claire, Vlamakis, Hera, Barteneva, Natasha, Paulson, Joseph N, Chai, Liraz, Clardy, Jon, Kolter, Roberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5148602/
https://www.ncbi.nlm.nih.gov/pubmed/27855786
http://dx.doi.org/10.7554/eLife.17473
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author Segev, Einat
Wyche, Thomas P
Kim, Ki Hyun
Petersen, Jörn
Ellebrandt, Claire
Vlamakis, Hera
Barteneva, Natasha
Paulson, Joseph N
Chai, Liraz
Clardy, Jon
Kolter, Roberto
author_facet Segev, Einat
Wyche, Thomas P
Kim, Ki Hyun
Petersen, Jörn
Ellebrandt, Claire
Vlamakis, Hera
Barteneva, Natasha
Paulson, Joseph N
Chai, Liraz
Clardy, Jon
Kolter, Roberto
author_sort Segev, Einat
collection PubMed
description Emiliania huxleyi is a model coccolithophore micro-alga that generates vast blooms in the ocean. Bacteria are not considered among the major factors influencing coccolithophore physiology. Here we show through a laboratory model system that the bacterium Phaeobacter inhibens, a well-studied member of the Roseobacter group, intimately interacts with E. huxleyi. While attached to the algal cell, bacteria initially promote algal growth but ultimately kill their algal host. Both algal growth enhancement and algal death are driven by the bacterially-produced phytohormone indole-3-acetic acid. Bacterial production of indole-3-acetic acid and attachment to algae are significantly increased by tryptophan, which is exuded from the algal cell. Algal death triggered by bacteria involves activation of pathways unique to oxidative stress response and programmed cell death. Our observations suggest that bacteria greatly influence the physiology and metabolism of E. huxleyi. Coccolithophore-bacteria interactions should be further studied in the environment to determine whether they impact micro-algal population dynamics on a global scale. DOI: http://dx.doi.org/10.7554/eLife.17473.001
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spelling pubmed-51486022016-12-12 Dynamic metabolic exchange governs a marine algal-bacterial interaction Segev, Einat Wyche, Thomas P Kim, Ki Hyun Petersen, Jörn Ellebrandt, Claire Vlamakis, Hera Barteneva, Natasha Paulson, Joseph N Chai, Liraz Clardy, Jon Kolter, Roberto eLife Ecology Emiliania huxleyi is a model coccolithophore micro-alga that generates vast blooms in the ocean. Bacteria are not considered among the major factors influencing coccolithophore physiology. Here we show through a laboratory model system that the bacterium Phaeobacter inhibens, a well-studied member of the Roseobacter group, intimately interacts with E. huxleyi. While attached to the algal cell, bacteria initially promote algal growth but ultimately kill their algal host. Both algal growth enhancement and algal death are driven by the bacterially-produced phytohormone indole-3-acetic acid. Bacterial production of indole-3-acetic acid and attachment to algae are significantly increased by tryptophan, which is exuded from the algal cell. Algal death triggered by bacteria involves activation of pathways unique to oxidative stress response and programmed cell death. Our observations suggest that bacteria greatly influence the physiology and metabolism of E. huxleyi. Coccolithophore-bacteria interactions should be further studied in the environment to determine whether they impact micro-algal population dynamics on a global scale. DOI: http://dx.doi.org/10.7554/eLife.17473.001 eLife Sciences Publications, Ltd 2016-11-18 /pmc/articles/PMC5148602/ /pubmed/27855786 http://dx.doi.org/10.7554/eLife.17473 Text en © 2016, Segev et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Ecology
Segev, Einat
Wyche, Thomas P
Kim, Ki Hyun
Petersen, Jörn
Ellebrandt, Claire
Vlamakis, Hera
Barteneva, Natasha
Paulson, Joseph N
Chai, Liraz
Clardy, Jon
Kolter, Roberto
Dynamic metabolic exchange governs a marine algal-bacterial interaction
title Dynamic metabolic exchange governs a marine algal-bacterial interaction
title_full Dynamic metabolic exchange governs a marine algal-bacterial interaction
title_fullStr Dynamic metabolic exchange governs a marine algal-bacterial interaction
title_full_unstemmed Dynamic metabolic exchange governs a marine algal-bacterial interaction
title_short Dynamic metabolic exchange governs a marine algal-bacterial interaction
title_sort dynamic metabolic exchange governs a marine algal-bacterial interaction
topic Ecology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5148602/
https://www.ncbi.nlm.nih.gov/pubmed/27855786
http://dx.doi.org/10.7554/eLife.17473
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