Experimental and theoretical support for costs of plasticity and phenotype in a nematode cannibalistic trait.

IF 3.4 1区 生物学 Q2 EVOLUTIONARY BIOLOGY Evolution Letters Pub Date : 2023-01-31 eCollection Date: 2023-02-01 DOI:10.1093/evlett/qrac001
Mohannad Dardiry, Veysi Piskobulu, Ata Kalirad, Ralf J Sommer
{"title":"Experimental and theoretical support for costs of plasticity and phenotype in a nematode cannibalistic trait.","authors":"Mohannad Dardiry, Veysi Piskobulu, Ata Kalirad, Ralf J Sommer","doi":"10.1093/evlett/qrac001","DOIUrl":null,"url":null,"abstract":"<p><p>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 <i>Pristionchus pacificus</i>, to experimentally measure these costs in wild isolates under controlled laboratory conditions. <i>P. pacificus</i> 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 <i>P. pacificus</i> phylogenetic tree. Then, we exposed <i>P. pacificus</i> 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 <i>P. pacificus</i>. 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.</p>","PeriodicalId":48629,"journal":{"name":"Evolution Letters","volume":"7 1","pages":"48-57"},"PeriodicalIF":3.4000,"publicationDate":"2023-01-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/96/e8/qrac001.PMC10091500.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Evolution Letters","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/evlett/qrac001","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/2/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"EVOLUTIONARY BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

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.

Abstract Image

Abstract Image

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
线虫食人性状的可塑性和表型成本的实验和理论支持。
发育可塑性是指基因型在不同环境条件下表现出多种表型的能力,已被证明能促进新性状的进化。然而,虽然理论上已经预测了可塑性的相关成本,即由于表达可塑性以应对环境变化的能力而造成的适应性损失,以及表型的成本,即由于在不同环境中表达固定表型而造成的适应性损失,但在经验上,这种成本仍然很少被记录和理解。在这里,我们利用雌雄同体线虫 Pristionchus pacificus 这一可塑性模型系统,在受控的实验室条件下实验性地测量了野生分离种的这些成本。在不同的外部刺激下,Pristionchus pacificus 可以形成细菌性摄食或捕食性口腔形态,不同品系之间的口腔形态比例存在自然差异。我们首先分析了太平洋栉水母系统发育树中繁殖力和发育速度与口部形态的关系,从而证明了表型的代价。然后,我们将太平洋栉水母菌株暴露于两种不同的微生物食物中,从而诱导出菌株特有的口型比例。我们的研究结果表明,可塑性品系确实要为可塑性付出代价,即饮食诱导的掠食性口型与繁殖力降低和发育速度减慢有关。与此相反,非可塑性菌株则要付出表型成本,因为它的表型并不会因为不利的细菌性食物而改变,但在有利的食物中却表现出更高的适应性和更快的发育速度。此外,我们还利用一个基于经验推导的生命史参数的阶段结构种群模型,展示了种群结构如何减轻太平洋鼠的可塑性成本。该模型的结果说明了与可塑性相关的成本及其对竞争的影响在多大程度上取决于生态因素。这项研究为基于经验和建模方法的可塑性和表型成本提供了支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Evolution Letters
Evolution Letters EVOLUTIONARY BIOLOGY-
CiteScore
13.00
自引率
2.00%
发文量
35
审稿时长
10 weeks
期刊介绍: Evolution Letters publishes cutting-edge new research in all areas of Evolutionary Biology. Available exclusively online, and entirely open access, Evolution Letters consists of Letters - original pieces of research which form the bulk of papers - and Comments and Opinion - a forum for highlighting timely new research ideas for the evolutionary community.
期刊最新文献
Antibiotic resistance alters the ability of Pseudomonas aeruginosa to invade bacteria from the respiratory microbiome. A biological circuit to anticipate trend. Testing the radiation cascade in postglacial radiations of whitefish and their parasites: founder events and host ecology drive parasite evolution. Sex chromosome turnover in hybridizing stickleback lineages. Adaptive alien genes are maintained amid a vanishing introgression footprint in a sea squirt.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1