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Experimental and theoretical support for costs of plasticity and phenotype in a nematode cannibalistic trait
Developmental plasticity is the ability of a genotype to express multiple phenotypes under different environmental conditions and has been shown to facilitate the evolution of novel traits. However, while the associated cost of plasticity, i.e., the loss in fitness due to the ability to express plas...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10091500/ https://www.ncbi.nlm.nih.gov/pubmed/37065436 http://dx.doi.org/10.1093/evlett/qrac001 |
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author | Dardiry, Mohannad Piskobulu, Veysi Kalirad, Ata Sommer, Ralf J |
author_facet | Dardiry, Mohannad Piskobulu, Veysi Kalirad, Ata Sommer, Ralf J |
author_sort | Dardiry, Mohannad |
collection | PubMed |
description | Developmental plasticity is the ability of a genotype to express multiple phenotypes under different environmental conditions and has been shown to facilitate the evolution of novel traits. However, while the associated cost of plasticity, i.e., the loss in fitness due to the ability to express plasticity in response to environmental change, and the cost of phenotype, i.e., the loss of fitness due to expressing a fixed phenotype across environments, have been theoretically predicted, empirically such costs remain poorly documented and little understood. Here, we use a plasticity model system, hermaphroditic nematode Pristionchus pacificus, to experimentally measure these costs in wild isolates under controlled laboratory conditions. P. pacificus can develop either a bacterial feeding or predatory mouth morph in response to different external stimuli, with natural variation of mouth-morph ratios between strains. We first demonstrated the cost of phenotype by analyzing fecundity and developmental speed in relation to mouth morphs across the P. pacificus phylogenetic tree. Then, we exposed P. pacificus strains to two distinct microbial diets that induce strain-specific mouth-form ratios. Our results indicate that the plastic strain does shoulder a cost of plasticity, i.e., the diet-induced predatory mouth morph is associated with reduced fecundity and slower developmental speed. In contrast, the non-plastic strain suffers from the cost of phenotype since its phenotype does not change to match the unfavorable bacterial diet but shows increased fitness and higher developmental speed on the favorable diet. Furthermore, using a stage-structured population model based on empirically derived life history parameters, we show how population structure can alleviate the cost of plasticity in P. pacificus. The results of the model illustrate the extent to which the costs associated with plasticity and its effect on competition depend on ecological factors. This study provides support for costs of plasticity and phenotype based on empirical and modeling approaches. |
format | Online Article Text |
id | pubmed-10091500 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-100915002023-04-13 Experimental and theoretical support for costs of plasticity and phenotype in a nematode cannibalistic trait Dardiry, Mohannad Piskobulu, Veysi Kalirad, Ata Sommer, Ralf J Evol Lett Letters Developmental plasticity is the ability of a genotype to express multiple phenotypes under different environmental conditions and has been shown to facilitate the evolution of novel traits. However, while the associated cost of plasticity, i.e., the loss in fitness due to the ability to express plasticity in response to environmental change, and the cost of phenotype, i.e., the loss of fitness due to expressing a fixed phenotype across environments, have been theoretically predicted, empirically such costs remain poorly documented and little understood. Here, we use a plasticity model system, hermaphroditic nematode Pristionchus pacificus, to experimentally measure these costs in wild isolates under controlled laboratory conditions. P. pacificus can develop either a bacterial feeding or predatory mouth morph in response to different external stimuli, with natural variation of mouth-morph ratios between strains. We first demonstrated the cost of phenotype by analyzing fecundity and developmental speed in relation to mouth morphs across the P. pacificus phylogenetic tree. Then, we exposed P. pacificus strains to two distinct microbial diets that induce strain-specific mouth-form ratios. Our results indicate that the plastic strain does shoulder a cost of plasticity, i.e., the diet-induced predatory mouth morph is associated with reduced fecundity and slower developmental speed. In contrast, the non-plastic strain suffers from the cost of phenotype since its phenotype does not change to match the unfavorable bacterial diet but shows increased fitness and higher developmental speed on the favorable diet. Furthermore, using a stage-structured population model based on empirically derived life history parameters, we show how population structure can alleviate the cost of plasticity in P. pacificus. The results of the model illustrate the extent to which the costs associated with plasticity and its effect on competition depend on ecological factors. This study provides support for costs of plasticity and phenotype based on empirical and modeling approaches. Oxford University Press 2023-01-31 /pmc/articles/PMC10091500/ /pubmed/37065436 http://dx.doi.org/10.1093/evlett/qrac001 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of The Society for the Study of Evolution (SSE) and European Society for Evolutionary Biology (ESEN). https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Letters Dardiry, Mohannad Piskobulu, Veysi Kalirad, Ata Sommer, Ralf J Experimental and theoretical support for costs of plasticity and phenotype in a nematode cannibalistic trait |
title | Experimental and theoretical support for costs of plasticity and phenotype in a nematode cannibalistic trait |
title_full | Experimental and theoretical support for costs of plasticity and phenotype in a nematode cannibalistic trait |
title_fullStr | Experimental and theoretical support for costs of plasticity and phenotype in a nematode cannibalistic trait |
title_full_unstemmed | Experimental and theoretical support for costs of plasticity and phenotype in a nematode cannibalistic trait |
title_short | Experimental and theoretical support for costs of plasticity and phenotype in a nematode cannibalistic trait |
title_sort | experimental and theoretical support for costs of plasticity and phenotype in a nematode cannibalistic trait |
topic | Letters |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10091500/ https://www.ncbi.nlm.nih.gov/pubmed/37065436 http://dx.doi.org/10.1093/evlett/qrac001 |
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