Cargando…

Chytrid parasitism facilitates trophic transfer between bloom-forming cyanobacteria and zooplankton (Daphnia)

Parasites are rarely included in food web studies, although they can strongly alter trophic interactions. In aquatic ecosystems, poorly grazed cyanobacteria often dominate phytoplankton communities, leading to the decoupling of primary and secondary production. Here, we addressed the interface betwe...

Descripción completa

Detalles Bibliográficos
Autores principales: Agha, Ramsy, Saebelfeld, Manja, Manthey, Christin, Rohrlack, Thomas, Wolinska, Justyna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5062065/
https://www.ncbi.nlm.nih.gov/pubmed/27733762
http://dx.doi.org/10.1038/srep35039
_version_ 1782459702779576320
author Agha, Ramsy
Saebelfeld, Manja
Manthey, Christin
Rohrlack, Thomas
Wolinska, Justyna
author_facet Agha, Ramsy
Saebelfeld, Manja
Manthey, Christin
Rohrlack, Thomas
Wolinska, Justyna
author_sort Agha, Ramsy
collection PubMed
description Parasites are rarely included in food web studies, although they can strongly alter trophic interactions. In aquatic ecosystems, poorly grazed cyanobacteria often dominate phytoplankton communities, leading to the decoupling of primary and secondary production. Here, we addressed the interface between predator-prey and host-parasite interactions by conducting a life-table experiment, in which four Daphnia galeata genotypes were maintained on quantitatively comparable diets consisting of healthy cyanobacteria or cyanobacteria infected by a fungal (chytrid) parasite. In four out of five fitness parameters, at least one Daphnia genotype performed better on parasitised cyanobacteria than in the absence of infection. Further treatments consisting of purified chytrid zoospores and heterotrophic bacteria suspensions established the causes of improved fitness. First, Daphnia feed on chytrid zoospores which trophically upgrade cyanobacterial carbon. Second, an increase in heterotrophic bacterial biomass, promoted by cyanobacterial decay, provides an additional food source for Daphnia. In addition, chytrid infection induces fragmentation of cyanobacterial filaments, which could render cyanobacteria more edible. Our results demonstrate that chytrid parasitism can sustain zooplankton under cyanobacterial bloom conditions, and exemplify the potential of parasites to alter interactions between trophic levels.
format Online
Article
Text
id pubmed-5062065
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-50620652016-10-24 Chytrid parasitism facilitates trophic transfer between bloom-forming cyanobacteria and zooplankton (Daphnia) Agha, Ramsy Saebelfeld, Manja Manthey, Christin Rohrlack, Thomas Wolinska, Justyna Sci Rep Article Parasites are rarely included in food web studies, although they can strongly alter trophic interactions. In aquatic ecosystems, poorly grazed cyanobacteria often dominate phytoplankton communities, leading to the decoupling of primary and secondary production. Here, we addressed the interface between predator-prey and host-parasite interactions by conducting a life-table experiment, in which four Daphnia galeata genotypes were maintained on quantitatively comparable diets consisting of healthy cyanobacteria or cyanobacteria infected by a fungal (chytrid) parasite. In four out of five fitness parameters, at least one Daphnia genotype performed better on parasitised cyanobacteria than in the absence of infection. Further treatments consisting of purified chytrid zoospores and heterotrophic bacteria suspensions established the causes of improved fitness. First, Daphnia feed on chytrid zoospores which trophically upgrade cyanobacterial carbon. Second, an increase in heterotrophic bacterial biomass, promoted by cyanobacterial decay, provides an additional food source for Daphnia. In addition, chytrid infection induces fragmentation of cyanobacterial filaments, which could render cyanobacteria more edible. Our results demonstrate that chytrid parasitism can sustain zooplankton under cyanobacterial bloom conditions, and exemplify the potential of parasites to alter interactions between trophic levels. Nature Publishing Group 2016-10-13 /pmc/articles/PMC5062065/ /pubmed/27733762 http://dx.doi.org/10.1038/srep35039 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Agha, Ramsy
Saebelfeld, Manja
Manthey, Christin
Rohrlack, Thomas
Wolinska, Justyna
Chytrid parasitism facilitates trophic transfer between bloom-forming cyanobacteria and zooplankton (Daphnia)
title Chytrid parasitism facilitates trophic transfer between bloom-forming cyanobacteria and zooplankton (Daphnia)
title_full Chytrid parasitism facilitates trophic transfer between bloom-forming cyanobacteria and zooplankton (Daphnia)
title_fullStr Chytrid parasitism facilitates trophic transfer between bloom-forming cyanobacteria and zooplankton (Daphnia)
title_full_unstemmed Chytrid parasitism facilitates trophic transfer between bloom-forming cyanobacteria and zooplankton (Daphnia)
title_short Chytrid parasitism facilitates trophic transfer between bloom-forming cyanobacteria and zooplankton (Daphnia)
title_sort chytrid parasitism facilitates trophic transfer between bloom-forming cyanobacteria and zooplankton (daphnia)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5062065/
https://www.ncbi.nlm.nih.gov/pubmed/27733762
http://dx.doi.org/10.1038/srep35039
work_keys_str_mv AT agharamsy chytridparasitismfacilitatestrophictransferbetweenbloomformingcyanobacteriaandzooplanktondaphnia
AT saebelfeldmanja chytridparasitismfacilitatestrophictransferbetweenbloomformingcyanobacteriaandzooplanktondaphnia
AT mantheychristin chytridparasitismfacilitatestrophictransferbetweenbloomformingcyanobacteriaandzooplanktondaphnia
AT rohrlackthomas chytridparasitismfacilitatestrophictransferbetweenbloomformingcyanobacteriaandzooplanktondaphnia
AT wolinskajustyna chytridparasitismfacilitatestrophictransferbetweenbloomformingcyanobacteriaandzooplanktondaphnia