Interactive effects of developmental and adult nutrition on lifespan and fecundity in a genetically diverse Drosophila population.

IF 2.6 3区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
PLoS ONE Pub Date : 2025-10-10 eCollection Date: 2025-01-01 DOI:10.1371/journal.pone.0334341
Andrew Jones, De'anne Donnell, Elizabeth G King, Enoch Ng'oma
{"title":"Interactive effects of developmental and adult nutrition on lifespan and fecundity in a genetically diverse Drosophila population.","authors":"Andrew Jones, De'anne Donnell, Elizabeth G King, Enoch Ng'oma","doi":"10.1371/journal.pone.0334341","DOIUrl":null,"url":null,"abstract":"<p><p>Developmental conditions, including temperature, diet, and parasite exposure, can shape adult fitness phenotypes across species. While studies often examine the independent effects of early-life and adult conditions on life history traits, fewer have focused on their interactive effects, particularly in genetically diverse populations. Here, we investigate how larval and adult diet interact to influence lifespan and fecundity in a genetically diverse population of Drosophila melanogaster. We manipulated protein availability across larval and adult stages and found significant larval-adult diet interactions affecting both traits, though in different ways. Several key patterns emerged, including age- and sex-specific effects, survival differences in the post-median life phase, shifts in the timing of peak fecundity, and sustained egg production in older stages. Protein reduction increased male maximum lifespan and female lifetime fecundity, while lower adult protein intake delayed egg-laying by approximately two weeks, particularly in flies that also experienced low developmental protein. These findings underscore the importance of assessing life history traits dynamically over time, as interactions between developmental and adult environments may drive complex, non-additive effects that are not apparent in cross-sectional measurements. Considering both additive and interactive effects in diverse genetic backgrounds will be critical for understanding the evolutionary and ecological consequences of nutritional variation.</p>","PeriodicalId":20189,"journal":{"name":"PLoS ONE","volume":"20 10","pages":"e0334341"},"PeriodicalIF":2.6000,"publicationDate":"2025-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12513662/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"PLoS ONE","FirstCategoryId":"103","ListUrlMain":"https://doi.org/10.1371/journal.pone.0334341","RegionNum":3,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Developmental conditions, including temperature, diet, and parasite exposure, can shape adult fitness phenotypes across species. While studies often examine the independent effects of early-life and adult conditions on life history traits, fewer have focused on their interactive effects, particularly in genetically diverse populations. Here, we investigate how larval and adult diet interact to influence lifespan and fecundity in a genetically diverse population of Drosophila melanogaster. We manipulated protein availability across larval and adult stages and found significant larval-adult diet interactions affecting both traits, though in different ways. Several key patterns emerged, including age- and sex-specific effects, survival differences in the post-median life phase, shifts in the timing of peak fecundity, and sustained egg production in older stages. Protein reduction increased male maximum lifespan and female lifetime fecundity, while lower adult protein intake delayed egg-laying by approximately two weeks, particularly in flies that also experienced low developmental protein. These findings underscore the importance of assessing life history traits dynamically over time, as interactions between developmental and adult environments may drive complex, non-additive effects that are not apparent in cross-sectional measurements. Considering both additive and interactive effects in diverse genetic backgrounds will be critical for understanding the evolutionary and ecological consequences of nutritional variation.

Abstract Image

Abstract Image

Abstract Image

发育和成体营养对遗传多样性果蝇种群寿命和繁殖力的相互作用。
发育条件,包括温度、饮食和寄生虫暴露,可以塑造跨物种的成年适应度表型。虽然研究经常检查早期生活和成年条件对生活史特征的独立影响,但很少关注它们的相互作用,特别是在基因多样化的人群中。在这里,我们研究了幼虫和成虫的饮食如何相互作用来影响遗传多样化的黑腹果蝇种群的寿命和繁殖力。我们控制了幼虫和成虫阶段的蛋白质利用率,发现幼虫-成虫饮食的显著相互作用影响了这两种特征,尽管方式不同。出现了几个关键模式,包括年龄和性别特异性影响,中位后生命阶段的生存差异,高峰繁殖力时间的变化,以及老年阶段持续的产卵。蛋白质的减少增加了雄性的最长寿命和雌性的终生繁殖力,而成虫蛋白质摄入量的减少使产卵延迟了大约两周,特别是在同样经历低发育蛋白的果蝇中。这些发现强调了随着时间的推移动态评估生活史特征的重要性,因为发育环境和成人环境之间的相互作用可能会驱动复杂的、非加性的效应,而这些效应在横断面测量中并不明显。考虑不同遗传背景下的加性和相互作用对理解营养变异的进化和生态后果至关重要。
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 求助全文
来源期刊
PLoS ONE
PLoS ONE 生物-生物学
CiteScore
6.20
自引率
5.40%
发文量
14242
审稿时长
3.7 months
期刊介绍: PLOS ONE is an international, peer-reviewed, open-access, online publication. PLOS ONE welcomes reports on primary research from any scientific discipline. It provides: * Open-access—freely accessible online, authors retain copyright * Fast publication times * Peer review by expert, practicing researchers * Post-publication tools to indicate quality and impact * Community-based dialogue on articles * Worldwide media coverage
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信