Metabolites limiting predator growth wane with prey biodiversity

IF 9.4 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES Proceedings of the National Academy of Sciences of the United States of America Pub Date : 2024-12-17 DOI:10.1073/pnas.2410210121
Gen Li, Ting Liu, Wangliang Xie, Zhenzhen Liu, Huixin Li, Joann K. Whalen, Alexandre Jousset, Zhong Wei
{"title":"Metabolites limiting predator growth wane with prey biodiversity","authors":"Gen Li, Ting Liu, Wangliang Xie, Zhenzhen Liu, Huixin Li, Joann K. Whalen, Alexandre Jousset, Zhong Wei","doi":"10.1073/pnas.2410210121","DOIUrl":null,"url":null,"abstract":"Predator–prey interactions are a major driver of microbiome dynamics, but remain difficult to predict. While several prey traits potentially impact resistance to predation, their effects in a multispecies context remain unclear. Here, we leverage synthetic bacterial communities of varying complexity to identify traits driving palatability for nematodes, a main consumer of bacteria in soil. We assessed trophic interactions between four nematode species and 122 bacterial isolates, across a gradient of prey biodiversity ranging from single species to 50 species. Nematode size, a proxy for prey palatability, varied strongly with prey community composition and could be predicted by metabolic and morphological properties of the prey. However, the influence of prey traits on predators depended on biodiversity. Secondary metabolites drove palatability in monoculture, but this effect vanished under increasing prey biodiversity, where prey size became the dominant predictors of nematode size. Although idiosyncratic properties are often emphasized in the literatures, our results suggest that in biodiverse assemblages, the composition of available prey and their traits are more reliable predictors of predator–prey interactions. This study offers valuable insights into microbial ecology in the context of predator–prey interactions, as cryptic microbial responses can be guided by deductions based on generalizable biological traits.","PeriodicalId":20548,"journal":{"name":"Proceedings of the National Academy of Sciences of the United States of America","volume":"13 1","pages":""},"PeriodicalIF":9.4000,"publicationDate":"2024-12-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Proceedings of the National Academy of Sciences of the United States of America","FirstCategoryId":"103","ListUrlMain":"https://doi.org/10.1073/pnas.2410210121","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Predator–prey interactions are a major driver of microbiome dynamics, but remain difficult to predict. While several prey traits potentially impact resistance to predation, their effects in a multispecies context remain unclear. Here, we leverage synthetic bacterial communities of varying complexity to identify traits driving palatability for nematodes, a main consumer of bacteria in soil. We assessed trophic interactions between four nematode species and 122 bacterial isolates, across a gradient of prey biodiversity ranging from single species to 50 species. Nematode size, a proxy for prey palatability, varied strongly with prey community composition and could be predicted by metabolic and morphological properties of the prey. However, the influence of prey traits on predators depended on biodiversity. Secondary metabolites drove palatability in monoculture, but this effect vanished under increasing prey biodiversity, where prey size became the dominant predictors of nematode size. Although idiosyncratic properties are often emphasized in the literatures, our results suggest that in biodiverse assemblages, the composition of available prey and their traits are more reliable predictors of predator–prey interactions. This study offers valuable insights into microbial ecology in the context of predator–prey interactions, as cryptic microbial responses can be guided by deductions based on generalizable biological traits.
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
限制捕食者生长的代谢物随着猎物生物多样性的减少而减少
捕食者-猎物相互作用是微生物组动力学的主要驱动因素,但仍然难以预测。虽然一些猎物特征可能会影响对捕食者的抵抗力,但它们在多物种环境中的影响尚不清楚。在这里,我们利用不同复杂性的合成细菌群落来识别驱动线虫适口性的特征,线虫是土壤中细菌的主要消费者。我们评估了4种线虫和122种细菌分离物之间的营养相互作用,跨越了猎物生物多样性从单一物种到50种的梯度。线虫的大小是表征猎物适口性的一个指标,它随猎物群落组成的变化强烈,可以通过猎物的代谢和形态特征来预测。然而,猎物性状对捕食者的影响取决于生物多样性。在单一养殖中,次生代谢物驱动了线虫的适口性,但在猎物生物多样性增加的情况下,这种影响消失了,猎物大小成为线虫大小的主要预测因子。虽然在文献中经常强调特质,但我们的研究结果表明,在生物多样性组合中,可用猎物的组成及其特征是捕食者-猎物相互作用的更可靠的预测因素。这项研究为捕食者-猎物相互作用背景下的微生物生态学提供了有价值的见解,因为基于可推广的生物学特征的推断可以指导隐微生物反应。
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
CiteScore
19.00
自引率
0.90%
发文量
3575
审稿时长
2.5 months
期刊介绍: The Proceedings of the National Academy of Sciences (PNAS), a peer-reviewed journal of the National Academy of Sciences (NAS), serves as an authoritative source for high-impact, original research across the biological, physical, and social sciences. With a global scope, the journal welcomes submissions from researchers worldwide, making it an inclusive platform for advancing scientific knowledge.
期刊最新文献
Correction for Rashid et al., Nonpathological inflammation drives the development of an avian flight adaptation. Correction for Yao et al., An organic electrochemical neuron for a neuromorphic perception system. Correction for Sibille et al., Efficient mapping of the thalamocortical monosynaptic connectivity in vivo by tangential insertions of high-density electrodes in the cortex. Correction for Chae et al., Vulnerability to natural disasters and sustainable consumption: Unraveling political and regional differences. Correction for Deng et al., A coadapted KNL1 and spindle assembly checkpoint axis orchestrates precise mitosis in Arabidopsis.
×
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