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Metabolic co-dependence drives the evolutionarily ancient Hydra–Chlorella symbiosis

Many multicellular organisms rely on symbiotic associations for support of metabolic activity, protection, or energy. Understanding the mechanisms involved in controlling such interactions remains a major challenge. In an unbiased approach we identified key players that control the symbiosis between...

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Autores principales: Hamada, Mayuko, Schröder, Katja, Bathia, Jay, Kürn, Ulrich, Fraune, Sebastian, Khalturina, Mariia, Khalturin, Konstantin, Shinzato, Chuya, Satoh, Nori, Bosch, Thomas CG
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2018
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6019070/
https://www.ncbi.nlm.nih.gov/pubmed/29848439
http://dx.doi.org/10.7554/eLife.35122
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author Hamada, Mayuko
Schröder, Katja
Bathia, Jay
Kürn, Ulrich
Fraune, Sebastian
Khalturina, Mariia
Khalturin, Konstantin
Shinzato, Chuya
Satoh, Nori
Bosch, Thomas CG
author_facet Hamada, Mayuko
Schröder, Katja
Bathia, Jay
Kürn, Ulrich
Fraune, Sebastian
Khalturina, Mariia
Khalturin, Konstantin
Shinzato, Chuya
Satoh, Nori
Bosch, Thomas CG
author_sort Hamada, Mayuko
collection PubMed
description Many multicellular organisms rely on symbiotic associations for support of metabolic activity, protection, or energy. Understanding the mechanisms involved in controlling such interactions remains a major challenge. In an unbiased approach we identified key players that control the symbiosis between Hydra viridissima and its photosynthetic symbiont Chlorella sp. A99. We discovered significant up-regulation of Hydra genes encoding a phosphate transporter and glutamine synthetase suggesting regulated nutrition supply between host and symbionts. Interestingly, supplementing the medium with glutamine temporarily supports in vitro growth of the otherwise obligate symbiotic Chlorella, indicating loss of autonomy and dependence on the host. Genome sequencing of Chlorella sp. A99 revealed a large number of amino acid transporters and a degenerated nitrate assimilation pathway, presumably as consequence of the adaptation to the host environment. Our observations portray ancient symbiotic interactions as a codependent partnership in which exchange of nutrients appears to be the primary driving force.
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spelling pubmed-60190702018-07-05 Metabolic co-dependence drives the evolutionarily ancient Hydra–Chlorella symbiosis Hamada, Mayuko Schröder, Katja Bathia, Jay Kürn, Ulrich Fraune, Sebastian Khalturina, Mariia Khalturin, Konstantin Shinzato, Chuya Satoh, Nori Bosch, Thomas CG eLife Evolutionary Biology Many multicellular organisms rely on symbiotic associations for support of metabolic activity, protection, or energy. Understanding the mechanisms involved in controlling such interactions remains a major challenge. In an unbiased approach we identified key players that control the symbiosis between Hydra viridissima and its photosynthetic symbiont Chlorella sp. A99. We discovered significant up-regulation of Hydra genes encoding a phosphate transporter and glutamine synthetase suggesting regulated nutrition supply between host and symbionts. Interestingly, supplementing the medium with glutamine temporarily supports in vitro growth of the otherwise obligate symbiotic Chlorella, indicating loss of autonomy and dependence on the host. Genome sequencing of Chlorella sp. A99 revealed a large number of amino acid transporters and a degenerated nitrate assimilation pathway, presumably as consequence of the adaptation to the host environment. Our observations portray ancient symbiotic interactions as a codependent partnership in which exchange of nutrients appears to be the primary driving force. eLife Sciences Publications, Ltd 2018-05-31 /pmc/articles/PMC6019070/ /pubmed/29848439 http://dx.doi.org/10.7554/eLife.35122 Text en © 2018, Hamada et al http://creativecommons.org/licenses/by/4.0/ 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 Evolutionary Biology
Hamada, Mayuko
Schröder, Katja
Bathia, Jay
Kürn, Ulrich
Fraune, Sebastian
Khalturina, Mariia
Khalturin, Konstantin
Shinzato, Chuya
Satoh, Nori
Bosch, Thomas CG
Metabolic co-dependence drives the evolutionarily ancient Hydra–Chlorella symbiosis
title Metabolic co-dependence drives the evolutionarily ancient Hydra–Chlorella symbiosis
title_full Metabolic co-dependence drives the evolutionarily ancient Hydra–Chlorella symbiosis
title_fullStr Metabolic co-dependence drives the evolutionarily ancient Hydra–Chlorella symbiosis
title_full_unstemmed Metabolic co-dependence drives the evolutionarily ancient Hydra–Chlorella symbiosis
title_short Metabolic co-dependence drives the evolutionarily ancient Hydra–Chlorella symbiosis
title_sort metabolic co-dependence drives the evolutionarily ancient hydra–chlorella symbiosis
topic Evolutionary Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6019070/
https://www.ncbi.nlm.nih.gov/pubmed/29848439
http://dx.doi.org/10.7554/eLife.35122
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