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Transgenerational plasticity alters parasite fitness in changing environments
Transgenerational plasticity can help organisms respond rapidly to changing environments. Most prior studies of transgenerational plasticity in host–parasite interactions have focused on the host, leaving us with a limited understanding of transgenerational plasticity of parasites. We tested whether...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cambridge University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10090760/ https://www.ncbi.nlm.nih.gov/pubmed/36043359 http://dx.doi.org/10.1017/S0031182022001056 |
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author | Sun, Syuan-Jyun Dziuba, Marcin K. Mclntire, Kristina M. Jaye, Riley N. Duffy, Meghan A. |
author_facet | Sun, Syuan-Jyun Dziuba, Marcin K. Mclntire, Kristina M. Jaye, Riley N. Duffy, Meghan A. |
author_sort | Sun, Syuan-Jyun |
collection | PubMed |
description | Transgenerational plasticity can help organisms respond rapidly to changing environments. Most prior studies of transgenerational plasticity in host–parasite interactions have focused on the host, leaving us with a limited understanding of transgenerational plasticity of parasites. We tested whether exposure to elevated temperatures while spores are developing can modify the ability of those spores to infect new hosts, as well as the growth and virulence of the next generation of parasites in the new host. We exposed Daphnia dentifera to its naturally co-occurring fungal parasite Metschnikowia bicuspidata, rearing the parasite at cooler (20°C) or warmer (24°C) temperatures and then, factorially, using those spores to infect at 20 and 24°C. Infections by parasites reared at warmer past temperatures produced more mature spores, but only when the current infections were at cooler temperatures. Moreover, the percentage of mature spores was impacted by both rearing and current temperatures, and was highest for infections with spores reared in a warmer environment that infected hosts in a cooler environment. In contrast, virulence was influenced only by current temperatures. These results demonstrate transgenerational plasticity of parasites in response to temperature changes, with fitness impacts that are dependent on both past and current environments. |
format | Online Article Text |
id | pubmed-10090760 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Cambridge University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-100907602023-04-13 Transgenerational plasticity alters parasite fitness in changing environments Sun, Syuan-Jyun Dziuba, Marcin K. Mclntire, Kristina M. Jaye, Riley N. Duffy, Meghan A. Parasitology Research Article Transgenerational plasticity can help organisms respond rapidly to changing environments. Most prior studies of transgenerational plasticity in host–parasite interactions have focused on the host, leaving us with a limited understanding of transgenerational plasticity of parasites. We tested whether exposure to elevated temperatures while spores are developing can modify the ability of those spores to infect new hosts, as well as the growth and virulence of the next generation of parasites in the new host. We exposed Daphnia dentifera to its naturally co-occurring fungal parasite Metschnikowia bicuspidata, rearing the parasite at cooler (20°C) or warmer (24°C) temperatures and then, factorially, using those spores to infect at 20 and 24°C. Infections by parasites reared at warmer past temperatures produced more mature spores, but only when the current infections were at cooler temperatures. Moreover, the percentage of mature spores was impacted by both rearing and current temperatures, and was highest for infections with spores reared in a warmer environment that infected hosts in a cooler environment. In contrast, virulence was influenced only by current temperatures. These results demonstrate transgenerational plasticity of parasites in response to temperature changes, with fitness impacts that are dependent on both past and current environments. Cambridge University Press 2022-09 2022-08-04 /pmc/articles/PMC10090760/ /pubmed/36043359 http://dx.doi.org/10.1017/S0031182022001056 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited. |
spellingShingle | Research Article Sun, Syuan-Jyun Dziuba, Marcin K. Mclntire, Kristina M. Jaye, Riley N. Duffy, Meghan A. Transgenerational plasticity alters parasite fitness in changing environments |
title | Transgenerational plasticity alters parasite fitness in changing environments |
title_full | Transgenerational plasticity alters parasite fitness in changing environments |
title_fullStr | Transgenerational plasticity alters parasite fitness in changing environments |
title_full_unstemmed | Transgenerational plasticity alters parasite fitness in changing environments |
title_short | Transgenerational plasticity alters parasite fitness in changing environments |
title_sort | transgenerational plasticity alters parasite fitness in changing environments |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10090760/ https://www.ncbi.nlm.nih.gov/pubmed/36043359 http://dx.doi.org/10.1017/S0031182022001056 |
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