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Evolving interactions between diazotrophic cyanobacterium and phage mediate nitrogen release and host competitive ability

Interactions between nitrogen-fixing (i.e. diazotrophic) cyanobacteria and their viruses, cyanophages, can have large-scale ecosystem effects. These effects are mediated by temporal alterations in nutrient availability in aquatic systems owing to the release of nitrogen and carbon sources from cells...

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Autores principales: Cairns, Johannes, Coloma, Sebastián, Sivonen, Kaarina, Hiltunen, Teppo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society Publishing 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5210698/
https://www.ncbi.nlm.nih.gov/pubmed/28083116
http://dx.doi.org/10.1098/rsos.160839
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author Cairns, Johannes
Coloma, Sebastián
Sivonen, Kaarina
Hiltunen, Teppo
author_facet Cairns, Johannes
Coloma, Sebastián
Sivonen, Kaarina
Hiltunen, Teppo
author_sort Cairns, Johannes
collection PubMed
description Interactions between nitrogen-fixing (i.e. diazotrophic) cyanobacteria and their viruses, cyanophages, can have large-scale ecosystem effects. These effects are mediated by temporal alterations in nutrient availability in aquatic systems owing to the release of nitrogen and carbon sources from cells lysed by phages, as well as by ecologically important changes in the diversity and fitness of cyanobacterial populations that evolve in the presence of phages. However, ecological and evolutionary feedbacks between phages and nitrogen-fixing cyanobacteria are still relative poorly understood. Here, we used an experimental evolution approach to test the effect of interactions between a common filamentous, nitrogen-fixing cyanobacterium (Nodularia sp.) and its phage on cellular nitrogen release and host properties. Ecological, community-level effects of phage-mediated nitrogen release were tested with a phytoplankton bioassay. We found that cyanobacterial nitrogen release increased significantly as a result of viral lysis, which was associated with enhanced growth of phytoplankton species in cell-free filtrates compared with phage-resistant host controls in which lysis and subsequent nutrient release did not occur after phage exposure. We also observed an ecologically important change among phage-evolved cyanobacteria with phage-resistant phenotypes, a short-filamentous morphotype with reduced buoyancy compared with the ancestral long-filamentous morphotype. Reduced buoyancy might decrease the ability of these morphotypes to compete for light compared with longer, more buoyant filaments. Together, these findings demonstrate the potential of cyanobacteria–phage interactions to affect ecosystem biogeochemical cycles and planktonic community dynamics.
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spelling pubmed-52106982017-01-12 Evolving interactions between diazotrophic cyanobacterium and phage mediate nitrogen release and host competitive ability Cairns, Johannes Coloma, Sebastián Sivonen, Kaarina Hiltunen, Teppo R Soc Open Sci Biology (Whole Organism) Interactions between nitrogen-fixing (i.e. diazotrophic) cyanobacteria and their viruses, cyanophages, can have large-scale ecosystem effects. These effects are mediated by temporal alterations in nutrient availability in aquatic systems owing to the release of nitrogen and carbon sources from cells lysed by phages, as well as by ecologically important changes in the diversity and fitness of cyanobacterial populations that evolve in the presence of phages. However, ecological and evolutionary feedbacks between phages and nitrogen-fixing cyanobacteria are still relative poorly understood. Here, we used an experimental evolution approach to test the effect of interactions between a common filamentous, nitrogen-fixing cyanobacterium (Nodularia sp.) and its phage on cellular nitrogen release and host properties. Ecological, community-level effects of phage-mediated nitrogen release were tested with a phytoplankton bioassay. We found that cyanobacterial nitrogen release increased significantly as a result of viral lysis, which was associated with enhanced growth of phytoplankton species in cell-free filtrates compared with phage-resistant host controls in which lysis and subsequent nutrient release did not occur after phage exposure. We also observed an ecologically important change among phage-evolved cyanobacteria with phage-resistant phenotypes, a short-filamentous morphotype with reduced buoyancy compared with the ancestral long-filamentous morphotype. Reduced buoyancy might decrease the ability of these morphotypes to compete for light compared with longer, more buoyant filaments. Together, these findings demonstrate the potential of cyanobacteria–phage interactions to affect ecosystem biogeochemical cycles and planktonic community dynamics. The Royal Society Publishing 2016-12-14 /pmc/articles/PMC5210698/ /pubmed/28083116 http://dx.doi.org/10.1098/rsos.160839 Text en © 2016 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Biology (Whole Organism)
Cairns, Johannes
Coloma, Sebastián
Sivonen, Kaarina
Hiltunen, Teppo
Evolving interactions between diazotrophic cyanobacterium and phage mediate nitrogen release and host competitive ability
title Evolving interactions between diazotrophic cyanobacterium and phage mediate nitrogen release and host competitive ability
title_full Evolving interactions between diazotrophic cyanobacterium and phage mediate nitrogen release and host competitive ability
title_fullStr Evolving interactions between diazotrophic cyanobacterium and phage mediate nitrogen release and host competitive ability
title_full_unstemmed Evolving interactions between diazotrophic cyanobacterium and phage mediate nitrogen release and host competitive ability
title_short Evolving interactions between diazotrophic cyanobacterium and phage mediate nitrogen release and host competitive ability
title_sort evolving interactions between diazotrophic cyanobacterium and phage mediate nitrogen release and host competitive ability
topic Biology (Whole Organism)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5210698/
https://www.ncbi.nlm.nih.gov/pubmed/28083116
http://dx.doi.org/10.1098/rsos.160839
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