Cargando…

Transgenerational plasticity in a zooplankton in response to elevated temperature and parasitism

Organisms are increasingly facing multiple stressors, which can simultaneously interact to cause unpredictable impacts compared with a single stressor alone. Recent evidence suggests that phenotypic plasticity can allow for rapid responses to altered environments, including biotic and abiotic stress...

Descripción completa

Detalles Bibliográficos
Autores principales: Sun, Syuan‐Jyun, Dziuba, Marcin K., Jaye, Riley N., Duffy, Meghan A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9897957/
https://www.ncbi.nlm.nih.gov/pubmed/36760704
http://dx.doi.org/10.1002/ece3.9767
_version_ 1784882352726474752
author Sun, Syuan‐Jyun
Dziuba, Marcin K.
Jaye, Riley N.
Duffy, Meghan A.
author_facet Sun, Syuan‐Jyun
Dziuba, Marcin K.
Jaye, Riley N.
Duffy, Meghan A.
author_sort Sun, Syuan‐Jyun
collection PubMed
description Organisms are increasingly facing multiple stressors, which can simultaneously interact to cause unpredictable impacts compared with a single stressor alone. Recent evidence suggests that phenotypic plasticity can allow for rapid responses to altered environments, including biotic and abiotic stressors, both within a generation and across generations (transgenerational plasticity). Parents can potentially “prime” their offspring to better cope with similar stressors or, alternatively, might produce offspring that are less fit because of energetic constraints. At present, it remains unclear exactly how biotic and abiotic stressors jointly mediate the responses of transgenerational plasticity and whether this plasticity is adaptive. Here, we test the effects of biotic and abiotic environmental changes on within‐ and transgenerational plasticity using a Daphnia–Metschnikowia zooplankton‐fungal parasite system. By exposing parents and their offspring consecutively to the single and combined effects of elevated temperature and parasite infection, we showed that transgenerational plasticity induced by temperature and parasite stress influenced host fecundity and lifespan; offsprings of mothers who were exposed to one of the stressors were better able to tolerate elevated temperature, compared with the offspring of mothers who were exposed to neither or both stressors. Yet, the negative effects caused by parasite infection were much stronger, and this greater reduction in host fitness was not mitigated by transgenerational plasticity. We also showed that elevated temperature led to a lower average immune response, and that the relationship between immune response and lifetime fecundity reversed under elevated temperature: the daughters of exposed mothers showed decreased fecundity with increased hemocyte production at ambient temperature but the opposite relationship at elevated temperature. Together, our results highlight the need to address questions at the interface of multiple stressors and transgenerational plasticity and the importance of considering multiple fitness‐associated traits when evaluating the adaptive value of transgenerational plasticity under changing environments.
format Online
Article
Text
id pubmed-9897957
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-98979572023-02-08 Transgenerational plasticity in a zooplankton in response to elevated temperature and parasitism Sun, Syuan‐Jyun Dziuba, Marcin K. Jaye, Riley N. Duffy, Meghan A. Ecol Evol Research Articles Organisms are increasingly facing multiple stressors, which can simultaneously interact to cause unpredictable impacts compared with a single stressor alone. Recent evidence suggests that phenotypic plasticity can allow for rapid responses to altered environments, including biotic and abiotic stressors, both within a generation and across generations (transgenerational plasticity). Parents can potentially “prime” their offspring to better cope with similar stressors or, alternatively, might produce offspring that are less fit because of energetic constraints. At present, it remains unclear exactly how biotic and abiotic stressors jointly mediate the responses of transgenerational plasticity and whether this plasticity is adaptive. Here, we test the effects of biotic and abiotic environmental changes on within‐ and transgenerational plasticity using a Daphnia–Metschnikowia zooplankton‐fungal parasite system. By exposing parents and their offspring consecutively to the single and combined effects of elevated temperature and parasite infection, we showed that transgenerational plasticity induced by temperature and parasite stress influenced host fecundity and lifespan; offsprings of mothers who were exposed to one of the stressors were better able to tolerate elevated temperature, compared with the offspring of mothers who were exposed to neither or both stressors. Yet, the negative effects caused by parasite infection were much stronger, and this greater reduction in host fitness was not mitigated by transgenerational plasticity. We also showed that elevated temperature led to a lower average immune response, and that the relationship between immune response and lifetime fecundity reversed under elevated temperature: the daughters of exposed mothers showed decreased fecundity with increased hemocyte production at ambient temperature but the opposite relationship at elevated temperature. Together, our results highlight the need to address questions at the interface of multiple stressors and transgenerational plasticity and the importance of considering multiple fitness‐associated traits when evaluating the adaptive value of transgenerational plasticity under changing environments. John Wiley and Sons Inc. 2023-02-03 /pmc/articles/PMC9897957/ /pubmed/36760704 http://dx.doi.org/10.1002/ece3.9767 Text en © 2023 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Sun, Syuan‐Jyun
Dziuba, Marcin K.
Jaye, Riley N.
Duffy, Meghan A.
Transgenerational plasticity in a zooplankton in response to elevated temperature and parasitism
title Transgenerational plasticity in a zooplankton in response to elevated temperature and parasitism
title_full Transgenerational plasticity in a zooplankton in response to elevated temperature and parasitism
title_fullStr Transgenerational plasticity in a zooplankton in response to elevated temperature and parasitism
title_full_unstemmed Transgenerational plasticity in a zooplankton in response to elevated temperature and parasitism
title_short Transgenerational plasticity in a zooplankton in response to elevated temperature and parasitism
title_sort transgenerational plasticity in a zooplankton in response to elevated temperature and parasitism
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9897957/
https://www.ncbi.nlm.nih.gov/pubmed/36760704
http://dx.doi.org/10.1002/ece3.9767
work_keys_str_mv AT sunsyuanjyun transgenerationalplasticityinazooplanktoninresponsetoelevatedtemperatureandparasitism
AT dziubamarcink transgenerationalplasticityinazooplanktoninresponsetoelevatedtemperatureandparasitism
AT jayerileyn transgenerationalplasticityinazooplanktoninresponsetoelevatedtemperatureandparasitism
AT duffymeghana transgenerationalplasticityinazooplanktoninresponsetoelevatedtemperatureandparasitism