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Flavobacterial exudates disrupt cell cycle progression and metabolism of the diatom Thalassiosira pseudonana

Phytoplankton and bacteria form the base of marine ecosystems and their interactions drive global biogeochemical cycles. The effects of bacteria and bacteria-produced compounds on diatoms range from synergistic to pathogenic and can affect the physiology and transcriptional patterns of the interacti...

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Autores principales: Bartolek, Zinka, Creveld, Shiri Graff van, Coesel, Sacha, Cain, Kelsy R., Schatz, Megan, Morales, Rhonda, Virginia Armbrust, E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9666458/
https://www.ncbi.nlm.nih.gov/pubmed/36104452
http://dx.doi.org/10.1038/s41396-022-01313-9
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author Bartolek, Zinka
Creveld, Shiri Graff van
Coesel, Sacha
Cain, Kelsy R.
Schatz, Megan
Morales, Rhonda
Virginia Armbrust, E.
author_facet Bartolek, Zinka
Creveld, Shiri Graff van
Coesel, Sacha
Cain, Kelsy R.
Schatz, Megan
Morales, Rhonda
Virginia Armbrust, E.
author_sort Bartolek, Zinka
collection PubMed
description Phytoplankton and bacteria form the base of marine ecosystems and their interactions drive global biogeochemical cycles. The effects of bacteria and bacteria-produced compounds on diatoms range from synergistic to pathogenic and can affect the physiology and transcriptional patterns of the interacting diatom. Here, we investigate physiological and transcriptional changes in the marine diatom Thalassiosira pseudonana induced by extracellular metabolites of a known antagonistic bacterium Croceibacter atlanticus. Mono-cultures of C. atlanticus released compounds that inhibited diatom cell division and elicited a distinctive morphology of enlarged cells with increased chloroplast content and enlarged nuclei, similar to what was previously observed when the diatom was co-cultured with live bacteria. The extracellular C. atlanticus metabolites induced transcriptional changes in diatom pathways that include recognition and signaling pathways, cell cycle regulation, carbohydrate and amino acid production, as well as cell wall stability. Phenotypic analysis showed a disruption in the diatom cell cycle progression and an increase in both intra- and extracellular carbohydrates in diatom cultures after bacterial exudate treatment. The transcriptional changes and corresponding phenotypes suggest that extracellular bacterial metabolites, produced independently of direct bacterial-diatom interaction, may modulate diatom metabolism in ways that support bacterial growth.
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spelling pubmed-96664582022-11-17 Flavobacterial exudates disrupt cell cycle progression and metabolism of the diatom Thalassiosira pseudonana Bartolek, Zinka Creveld, Shiri Graff van Coesel, Sacha Cain, Kelsy R. Schatz, Megan Morales, Rhonda Virginia Armbrust, E. ISME J Article Phytoplankton and bacteria form the base of marine ecosystems and their interactions drive global biogeochemical cycles. The effects of bacteria and bacteria-produced compounds on diatoms range from synergistic to pathogenic and can affect the physiology and transcriptional patterns of the interacting diatom. Here, we investigate physiological and transcriptional changes in the marine diatom Thalassiosira pseudonana induced by extracellular metabolites of a known antagonistic bacterium Croceibacter atlanticus. Mono-cultures of C. atlanticus released compounds that inhibited diatom cell division and elicited a distinctive morphology of enlarged cells with increased chloroplast content and enlarged nuclei, similar to what was previously observed when the diatom was co-cultured with live bacteria. The extracellular C. atlanticus metabolites induced transcriptional changes in diatom pathways that include recognition and signaling pathways, cell cycle regulation, carbohydrate and amino acid production, as well as cell wall stability. Phenotypic analysis showed a disruption in the diatom cell cycle progression and an increase in both intra- and extracellular carbohydrates in diatom cultures after bacterial exudate treatment. The transcriptional changes and corresponding phenotypes suggest that extracellular bacterial metabolites, produced independently of direct bacterial-diatom interaction, may modulate diatom metabolism in ways that support bacterial growth. Nature Publishing Group UK 2022-09-14 2022-12 /pmc/articles/PMC9666458/ /pubmed/36104452 http://dx.doi.org/10.1038/s41396-022-01313-9 Text en © The Author(s) 2022 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/) .
spellingShingle Article
Bartolek, Zinka
Creveld, Shiri Graff van
Coesel, Sacha
Cain, Kelsy R.
Schatz, Megan
Morales, Rhonda
Virginia Armbrust, E.
Flavobacterial exudates disrupt cell cycle progression and metabolism of the diatom Thalassiosira pseudonana
title Flavobacterial exudates disrupt cell cycle progression and metabolism of the diatom Thalassiosira pseudonana
title_full Flavobacterial exudates disrupt cell cycle progression and metabolism of the diatom Thalassiosira pseudonana
title_fullStr Flavobacterial exudates disrupt cell cycle progression and metabolism of the diatom Thalassiosira pseudonana
title_full_unstemmed Flavobacterial exudates disrupt cell cycle progression and metabolism of the diatom Thalassiosira pseudonana
title_short Flavobacterial exudates disrupt cell cycle progression and metabolism of the diatom Thalassiosira pseudonana
title_sort flavobacterial exudates disrupt cell cycle progression and metabolism of the diatom thalassiosira pseudonana
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9666458/
https://www.ncbi.nlm.nih.gov/pubmed/36104452
http://dx.doi.org/10.1038/s41396-022-01313-9
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