Cargando…
Seasonality of parasitic and saprotrophic zoosporic fungi: linking sequence data to ecological traits
Zoosporic fungi of the phylum Chytridiomycota (chytrids) regularly dominate pelagic fungal communities in freshwater and marine environments. Their lifestyles range from obligate parasites to saprophytes. Yet, linking the scarce available sequence data to specific ecological traits or their host ran...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9381765/ https://www.ncbi.nlm.nih.gov/pubmed/35764676 http://dx.doi.org/10.1038/s41396-022-01267-y |
_version_ | 1784769146530037760 |
---|---|
author | Van den Wyngaert, Silke Ganzert, Lars Seto, Kensuke Rojas-Jimenez, Keilor Agha, Ramsy Berger, Stella A. Woodhouse, Jason Padisak, Judit Wurzbacher, Christian Kagami, Maiko Grossart, Hans-Peter |
author_facet | Van den Wyngaert, Silke Ganzert, Lars Seto, Kensuke Rojas-Jimenez, Keilor Agha, Ramsy Berger, Stella A. Woodhouse, Jason Padisak, Judit Wurzbacher, Christian Kagami, Maiko Grossart, Hans-Peter |
author_sort | Van den Wyngaert, Silke |
collection | PubMed |
description | Zoosporic fungi of the phylum Chytridiomycota (chytrids) regularly dominate pelagic fungal communities in freshwater and marine environments. Their lifestyles range from obligate parasites to saprophytes. Yet, linking the scarce available sequence data to specific ecological traits or their host ranges constitutes currently a major challenge. We combined 28 S rRNA gene amplicon sequencing with targeted isolation and sequencing approaches, along with cross-infection assays and analysis of chytrid infection prevalence to obtain new insights into chytrid diversity, ecology, and seasonal dynamics in a temperate lake. Parasitic phytoplankton-chytrid and saprotrophic pollen-chytrid interactions made up the majority of zoosporic fungal reads. We explicitly demonstrate the recurrent dominance of parasitic chytrids during frequent diatom blooms and saprotrophic chytrids during pollen rains. Distinct temporal dynamics of diatom-specific parasitic clades suggest mechanisms of coexistence based on niche differentiation and competitive strategies. The molecular and ecological information on chytrids generated in this study will aid further exploration of their spatial and temporal distribution patterns worldwide. To fully exploit the power of environmental sequencing for studies on chytrid ecology and evolution, we emphasize the need to intensify current isolation efforts of chytrids and integrate taxonomic and autecological data into long-term studies and experiments. |
format | Online Article Text |
id | pubmed-9381765 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-93817652022-08-18 Seasonality of parasitic and saprotrophic zoosporic fungi: linking sequence data to ecological traits Van den Wyngaert, Silke Ganzert, Lars Seto, Kensuke Rojas-Jimenez, Keilor Agha, Ramsy Berger, Stella A. Woodhouse, Jason Padisak, Judit Wurzbacher, Christian Kagami, Maiko Grossart, Hans-Peter ISME J Article Zoosporic fungi of the phylum Chytridiomycota (chytrids) regularly dominate pelagic fungal communities in freshwater and marine environments. Their lifestyles range from obligate parasites to saprophytes. Yet, linking the scarce available sequence data to specific ecological traits or their host ranges constitutes currently a major challenge. We combined 28 S rRNA gene amplicon sequencing with targeted isolation and sequencing approaches, along with cross-infection assays and analysis of chytrid infection prevalence to obtain new insights into chytrid diversity, ecology, and seasonal dynamics in a temperate lake. Parasitic phytoplankton-chytrid and saprotrophic pollen-chytrid interactions made up the majority of zoosporic fungal reads. We explicitly demonstrate the recurrent dominance of parasitic chytrids during frequent diatom blooms and saprotrophic chytrids during pollen rains. Distinct temporal dynamics of diatom-specific parasitic clades suggest mechanisms of coexistence based on niche differentiation and competitive strategies. The molecular and ecological information on chytrids generated in this study will aid further exploration of their spatial and temporal distribution patterns worldwide. To fully exploit the power of environmental sequencing for studies on chytrid ecology and evolution, we emphasize the need to intensify current isolation efforts of chytrids and integrate taxonomic and autecological data into long-term studies and experiments. Nature Publishing Group UK 2022-06-28 2022-09 /pmc/articles/PMC9381765/ /pubmed/35764676 http://dx.doi.org/10.1038/s41396-022-01267-y 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Van den Wyngaert, Silke Ganzert, Lars Seto, Kensuke Rojas-Jimenez, Keilor Agha, Ramsy Berger, Stella A. Woodhouse, Jason Padisak, Judit Wurzbacher, Christian Kagami, Maiko Grossart, Hans-Peter Seasonality of parasitic and saprotrophic zoosporic fungi: linking sequence data to ecological traits |
title | Seasonality of parasitic and saprotrophic zoosporic fungi: linking sequence data to ecological traits |
title_full | Seasonality of parasitic and saprotrophic zoosporic fungi: linking sequence data to ecological traits |
title_fullStr | Seasonality of parasitic and saprotrophic zoosporic fungi: linking sequence data to ecological traits |
title_full_unstemmed | Seasonality of parasitic and saprotrophic zoosporic fungi: linking sequence data to ecological traits |
title_short | Seasonality of parasitic and saprotrophic zoosporic fungi: linking sequence data to ecological traits |
title_sort | seasonality of parasitic and saprotrophic zoosporic fungi: linking sequence data to ecological traits |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9381765/ https://www.ncbi.nlm.nih.gov/pubmed/35764676 http://dx.doi.org/10.1038/s41396-022-01267-y |
work_keys_str_mv | AT vandenwyngaertsilke seasonalityofparasiticandsaprotrophiczoosporicfungilinkingsequencedatatoecologicaltraits AT ganzertlars seasonalityofparasiticandsaprotrophiczoosporicfungilinkingsequencedatatoecologicaltraits AT setokensuke seasonalityofparasiticandsaprotrophiczoosporicfungilinkingsequencedatatoecologicaltraits AT rojasjimenezkeilor seasonalityofparasiticandsaprotrophiczoosporicfungilinkingsequencedatatoecologicaltraits AT agharamsy seasonalityofparasiticandsaprotrophiczoosporicfungilinkingsequencedatatoecologicaltraits AT bergerstellaa seasonalityofparasiticandsaprotrophiczoosporicfungilinkingsequencedatatoecologicaltraits AT woodhousejason seasonalityofparasiticandsaprotrophiczoosporicfungilinkingsequencedatatoecologicaltraits AT padisakjudit seasonalityofparasiticandsaprotrophiczoosporicfungilinkingsequencedatatoecologicaltraits AT wurzbacherchristian seasonalityofparasiticandsaprotrophiczoosporicfungilinkingsequencedatatoecologicaltraits AT kagamimaiko seasonalityofparasiticandsaprotrophiczoosporicfungilinkingsequencedatatoecologicaltraits AT grossarthanspeter seasonalityofparasiticandsaprotrophiczoosporicfungilinkingsequencedatatoecologicaltraits |