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Cascading effects of prey identity on gene expression in a kleptoplastidic ciliate
Kleptoplastidic, or chloroplast stealing, lineages transiently retain functional photosynthetic machinery from algal prey. This machinery, and its photosynthetic outputs, must be integrated into the host's metabolism, but the details of this integration are poorly understood. Here, we study thi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10087830/ https://www.ncbi.nlm.nih.gov/pubmed/35975609 http://dx.doi.org/10.1111/jeu.12940 |
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author | Paight, Christopher Johnson, Matthew D. Lasek‐Nesselquist, Erica Moeller, Holly V. |
author_facet | Paight, Christopher Johnson, Matthew D. Lasek‐Nesselquist, Erica Moeller, Holly V. |
author_sort | Paight, Christopher |
collection | PubMed |
description | Kleptoplastidic, or chloroplast stealing, lineages transiently retain functional photosynthetic machinery from algal prey. This machinery, and its photosynthetic outputs, must be integrated into the host's metabolism, but the details of this integration are poorly understood. Here, we study this metabolic integration in the ciliate Mesodinium chamaeleon, a coastal marine species capable of retaining chloroplasts from at least six distinct genera of cryptophyte algae. To assess the effects of feeding history on ciliate physiology and gene expression, we acclimated M. chamaeleon to four different types of prey and contrasted well‐fed and starved treatments. Consistent with previous physiological work on the ciliate, we found that starved ciliates had lower chlorophyll content, photosynthetic rates, and growth rates than their well‐fed counterparts. However, ciliate gene expression mirrored prey phylogenetic relationships rather than physiological status, suggesting that, even as M. chamaeleon cells were starved of prey, their overarching regulatory systems remained tuned to the prey type to which they had been acclimated. Collectively, our results indicate a surprising degree of prey‐specific host transcriptional adjustments, implying varied integration of prey metabolic potential into many aspects of ciliate physiology. |
format | Online Article Text |
id | pubmed-10087830 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100878302023-04-12 Cascading effects of prey identity on gene expression in a kleptoplastidic ciliate Paight, Christopher Johnson, Matthew D. Lasek‐Nesselquist, Erica Moeller, Holly V. J Eukaryot Microbiol Original Articles Kleptoplastidic, or chloroplast stealing, lineages transiently retain functional photosynthetic machinery from algal prey. This machinery, and its photosynthetic outputs, must be integrated into the host's metabolism, but the details of this integration are poorly understood. Here, we study this metabolic integration in the ciliate Mesodinium chamaeleon, a coastal marine species capable of retaining chloroplasts from at least six distinct genera of cryptophyte algae. To assess the effects of feeding history on ciliate physiology and gene expression, we acclimated M. chamaeleon to four different types of prey and contrasted well‐fed and starved treatments. Consistent with previous physiological work on the ciliate, we found that starved ciliates had lower chlorophyll content, photosynthetic rates, and growth rates than their well‐fed counterparts. However, ciliate gene expression mirrored prey phylogenetic relationships rather than physiological status, suggesting that, even as M. chamaeleon cells were starved of prey, their overarching regulatory systems remained tuned to the prey type to which they had been acclimated. Collectively, our results indicate a surprising degree of prey‐specific host transcriptional adjustments, implying varied integration of prey metabolic potential into many aspects of ciliate physiology. John Wiley and Sons Inc. 2022-09-01 2023 /pmc/articles/PMC10087830/ /pubmed/35975609 http://dx.doi.org/10.1111/jeu.12940 Text en © 2022 The Authors. Journal of Eukaryotic Microbiology published by Wiley Periodicals LLC on behalf of International Society of Protistologists. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Paight, Christopher Johnson, Matthew D. Lasek‐Nesselquist, Erica Moeller, Holly V. Cascading effects of prey identity on gene expression in a kleptoplastidic ciliate |
title | Cascading effects of prey identity on gene expression in a kleptoplastidic ciliate |
title_full | Cascading effects of prey identity on gene expression in a kleptoplastidic ciliate |
title_fullStr | Cascading effects of prey identity on gene expression in a kleptoplastidic ciliate |
title_full_unstemmed | Cascading effects of prey identity on gene expression in a kleptoplastidic ciliate |
title_short | Cascading effects of prey identity on gene expression in a kleptoplastidic ciliate |
title_sort | cascading effects of prey identity on gene expression in a kleptoplastidic ciliate |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10087830/ https://www.ncbi.nlm.nih.gov/pubmed/35975609 http://dx.doi.org/10.1111/jeu.12940 |
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