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Sequential host-bacteria and bacteria-bacteria interactions determine the microbiome establishment of Nematostella vectensis

BACKGROUND: The microbiota of multicellular organisms undergoes considerable changes during host ontogeny but the general mechanisms that control community assembly and succession are poorly understood. Here, we use bacterial recolonization experiments in Nematostella vectensis as a model to underst...

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Autores principales: Domin, H., Zimmermann, J., Taubenheim, J., Fuentes Reyes, G., Saueressig, L., Prasse, D., Höppner, M., Schmitz, R. A., Hentschel, U., Kaleta, C., Fraune, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10656924/
https://www.ncbi.nlm.nih.gov/pubmed/37978412
http://dx.doi.org/10.1186/s40168-023-01701-z
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author Domin, H.
Zimmermann, J.
Taubenheim, J.
Fuentes Reyes, G.
Saueressig, L.
Prasse, D.
Höppner, M.
Schmitz, R. A.
Hentschel, U.
Kaleta, C.
Fraune, S.
author_facet Domin, H.
Zimmermann, J.
Taubenheim, J.
Fuentes Reyes, G.
Saueressig, L.
Prasse, D.
Höppner, M.
Schmitz, R. A.
Hentschel, U.
Kaleta, C.
Fraune, S.
author_sort Domin, H.
collection PubMed
description BACKGROUND: The microbiota of multicellular organisms undergoes considerable changes during host ontogeny but the general mechanisms that control community assembly and succession are poorly understood. Here, we use bacterial recolonization experiments in Nematostella vectensis as a model to understand general mechanisms determining bacterial establishment and succession. We compared the dynamic establishment of the microbiome on the germfree host and on inert silicone tubes. RESULTS: Following the dynamic reconstruction of microbial communities on both substrates, we show that the initial colonization events are strongly influenced by the host but not by the silicone tube, while the subsequent bacteria-bacteria interactions are the main driver of bacterial succession. Interestingly, the recolonization pattern on adult hosts resembles the ontogenetic colonization succession. This process occurs independently of the bacterial composition of the inoculum and can be followed at the level of individual bacteria. To identify potential metabolic traits associated with initial colonization success and potential metabolic interactions among bacteria associated with bacterial succession, we reconstructed the metabolic networks of bacterial colonizers based on their genomes. These analyses revealed that bacterial metabolic capabilities reflect the recolonization pattern, and the degradation of chitin might be a selection factor during early recolonization of the animal. Concurrently, transcriptomic analyses revealed that Nematostella possesses two chitin synthase genes, one of which is upregulated during early recolonization. CONCLUSIONS: Our results show that early recolonization events are strongly controlled by the host while subsequent colonization depends on metabolic bacteria-bacteria interactions largely independent of host ontogeny. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-023-01701-z.
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spelling pubmed-106569242023-11-18 Sequential host-bacteria and bacteria-bacteria interactions determine the microbiome establishment of Nematostella vectensis Domin, H. Zimmermann, J. Taubenheim, J. Fuentes Reyes, G. Saueressig, L. Prasse, D. Höppner, M. Schmitz, R. A. Hentschel, U. Kaleta, C. Fraune, S. Microbiome Research BACKGROUND: The microbiota of multicellular organisms undergoes considerable changes during host ontogeny but the general mechanisms that control community assembly and succession are poorly understood. Here, we use bacterial recolonization experiments in Nematostella vectensis as a model to understand general mechanisms determining bacterial establishment and succession. We compared the dynamic establishment of the microbiome on the germfree host and on inert silicone tubes. RESULTS: Following the dynamic reconstruction of microbial communities on both substrates, we show that the initial colonization events are strongly influenced by the host but not by the silicone tube, while the subsequent bacteria-bacteria interactions are the main driver of bacterial succession. Interestingly, the recolonization pattern on adult hosts resembles the ontogenetic colonization succession. This process occurs independently of the bacterial composition of the inoculum and can be followed at the level of individual bacteria. To identify potential metabolic traits associated with initial colonization success and potential metabolic interactions among bacteria associated with bacterial succession, we reconstructed the metabolic networks of bacterial colonizers based on their genomes. These analyses revealed that bacterial metabolic capabilities reflect the recolonization pattern, and the degradation of chitin might be a selection factor during early recolonization of the animal. Concurrently, transcriptomic analyses revealed that Nematostella possesses two chitin synthase genes, one of which is upregulated during early recolonization. CONCLUSIONS: Our results show that early recolonization events are strongly controlled by the host while subsequent colonization depends on metabolic bacteria-bacteria interactions largely independent of host ontogeny. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-023-01701-z. BioMed Central 2023-11-18 /pmc/articles/PMC10656924/ /pubmed/37978412 http://dx.doi.org/10.1186/s40168-023-01701-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Domin, H.
Zimmermann, J.
Taubenheim, J.
Fuentes Reyes, G.
Saueressig, L.
Prasse, D.
Höppner, M.
Schmitz, R. A.
Hentschel, U.
Kaleta, C.
Fraune, S.
Sequential host-bacteria and bacteria-bacteria interactions determine the microbiome establishment of Nematostella vectensis
title Sequential host-bacteria and bacteria-bacteria interactions determine the microbiome establishment of Nematostella vectensis
title_full Sequential host-bacteria and bacteria-bacteria interactions determine the microbiome establishment of Nematostella vectensis
title_fullStr Sequential host-bacteria and bacteria-bacteria interactions determine the microbiome establishment of Nematostella vectensis
title_full_unstemmed Sequential host-bacteria and bacteria-bacteria interactions determine the microbiome establishment of Nematostella vectensis
title_short Sequential host-bacteria and bacteria-bacteria interactions determine the microbiome establishment of Nematostella vectensis
title_sort sequential host-bacteria and bacteria-bacteria interactions determine the microbiome establishment of nematostella vectensis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10656924/
https://www.ncbi.nlm.nih.gov/pubmed/37978412
http://dx.doi.org/10.1186/s40168-023-01701-z
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