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The succession of epiphytic microalgae conditions fungal community composition: how chytrids respond to blooms of dinoflagellates

This study aims to investigate the temporal dynamics of the epiphytic protist community on macroalgae, during the summer months, with a specific focus on fungi, and the interactions between zoosporic chytrid parasites and the proliferation of the dinoflagellates. We employed a combination of environ...

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Autores principales: Fernández-Valero, Alan Denis, Reñé, Albert, Timoneda, Natàlia, Pou-Solà, Núria, Gordi, Jordina, Sampedro, Nagore, Garcés, Esther
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10522651/
https://www.ncbi.nlm.nih.gov/pubmed/37752353
http://dx.doi.org/10.1038/s43705-023-00304-x
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author Fernández-Valero, Alan Denis
Reñé, Albert
Timoneda, Natàlia
Pou-Solà, Núria
Gordi, Jordina
Sampedro, Nagore
Garcés, Esther
author_facet Fernández-Valero, Alan Denis
Reñé, Albert
Timoneda, Natàlia
Pou-Solà, Núria
Gordi, Jordina
Sampedro, Nagore
Garcés, Esther
author_sort Fernández-Valero, Alan Denis
collection PubMed
description This study aims to investigate the temporal dynamics of the epiphytic protist community on macroalgae, during the summer months, with a specific focus on fungi, and the interactions between zoosporic chytrid parasites and the proliferation of the dinoflagellates. We employed a combination of environmental sequencing techniques, incubation of natural samples, isolation of target organisms and laboratory experiments. Metabarcoding sequencing revealed changes in the dominant members of the epiphytic fungal community. Initially, fungi comprised < 1% of the protist community, mostly accounted for by Basidiomycota and Ascomycota, but with the emergence of Chytridiomycota during the mature phase of the biofilm, the fungal contribution increased to almost 30%. Chytridiomycota became dominant in parallel with an increase in the relative abundance of dinoflagellates in the community. Microscopy observations showed a general presence of chytrids following the peak proliferation of the dinoflagellate Ostreopsis sp., with the parasite, D. arenysensis as the dominant chytrid. The maximum infection prevalence was 2% indicating host-parasite coexistence. To further understand the in-situ prevalence of chytrids, we characterised the dynamics of the host abundance and prevalence of chytrids through co-culture. These laboratory experiments revealed intraspecific variability of D. arenysensis in its interaction with Ostreopsis, exhibiting a range from stable coexistence to the near-extinction of the host population. Moreover, while chytrids preferentially parasitized dinoflagellate cells, one of the strains examined displayed the ability to utilize pollen as a resource to maintain its viability, thus illustrating a facultative parasitic lifestyle. Our findings not only enrich our understanding of the diversity, ecology, and progression of epiphytic microalgal and fungal communities on Mediterranean coastal macroalgae, but they also shed light on the presence of zoosporic parasites in less-explored benthic habitats.
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spelling pubmed-105226512023-09-28 The succession of epiphytic microalgae conditions fungal community composition: how chytrids respond to blooms of dinoflagellates Fernández-Valero, Alan Denis Reñé, Albert Timoneda, Natàlia Pou-Solà, Núria Gordi, Jordina Sampedro, Nagore Garcés, Esther ISME Commun Article This study aims to investigate the temporal dynamics of the epiphytic protist community on macroalgae, during the summer months, with a specific focus on fungi, and the interactions between zoosporic chytrid parasites and the proliferation of the dinoflagellates. We employed a combination of environmental sequencing techniques, incubation of natural samples, isolation of target organisms and laboratory experiments. Metabarcoding sequencing revealed changes in the dominant members of the epiphytic fungal community. Initially, fungi comprised < 1% of the protist community, mostly accounted for by Basidiomycota and Ascomycota, but with the emergence of Chytridiomycota during the mature phase of the biofilm, the fungal contribution increased to almost 30%. Chytridiomycota became dominant in parallel with an increase in the relative abundance of dinoflagellates in the community. Microscopy observations showed a general presence of chytrids following the peak proliferation of the dinoflagellate Ostreopsis sp., with the parasite, D. arenysensis as the dominant chytrid. The maximum infection prevalence was 2% indicating host-parasite coexistence. To further understand the in-situ prevalence of chytrids, we characterised the dynamics of the host abundance and prevalence of chytrids through co-culture. These laboratory experiments revealed intraspecific variability of D. arenysensis in its interaction with Ostreopsis, exhibiting a range from stable coexistence to the near-extinction of the host population. Moreover, while chytrids preferentially parasitized dinoflagellate cells, one of the strains examined displayed the ability to utilize pollen as a resource to maintain its viability, thus illustrating a facultative parasitic lifestyle. Our findings not only enrich our understanding of the diversity, ecology, and progression of epiphytic microalgal and fungal communities on Mediterranean coastal macroalgae, but they also shed light on the presence of zoosporic parasites in less-explored benthic habitats. Nature Publishing Group UK 2023-09-26 /pmc/articles/PMC10522651/ /pubmed/37752353 http://dx.doi.org/10.1038/s43705-023-00304-x 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/) .
spellingShingle Article
Fernández-Valero, Alan Denis
Reñé, Albert
Timoneda, Natàlia
Pou-Solà, Núria
Gordi, Jordina
Sampedro, Nagore
Garcés, Esther
The succession of epiphytic microalgae conditions fungal community composition: how chytrids respond to blooms of dinoflagellates
title The succession of epiphytic microalgae conditions fungal community composition: how chytrids respond to blooms of dinoflagellates
title_full The succession of epiphytic microalgae conditions fungal community composition: how chytrids respond to blooms of dinoflagellates
title_fullStr The succession of epiphytic microalgae conditions fungal community composition: how chytrids respond to blooms of dinoflagellates
title_full_unstemmed The succession of epiphytic microalgae conditions fungal community composition: how chytrids respond to blooms of dinoflagellates
title_short The succession of epiphytic microalgae conditions fungal community composition: how chytrids respond to blooms of dinoflagellates
title_sort succession of epiphytic microalgae conditions fungal community composition: how chytrids respond to blooms of dinoflagellates
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10522651/
https://www.ncbi.nlm.nih.gov/pubmed/37752353
http://dx.doi.org/10.1038/s43705-023-00304-x
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