Bacteria-phage (co)evolution is constrained in a synthetic community across multiple bacteria-phage pairs.

IF 2.6 4区 生物学 Q3 MICROBIOLOGY
Meaghan Castledine, Daniel Padfield, Marli Schoeman, Amy Berry, Angus Buckling
{"title":"Bacteria-phage (co)evolution is constrained in a synthetic community across multiple bacteria-phage pairs.","authors":"Meaghan Castledine, Daniel Padfield, Marli Schoeman, Amy Berry, Angus Buckling","doi":"10.1099/mic.0.001577","DOIUrl":null,"url":null,"abstract":"<p><p>Bacteriophages can be important drivers of bacterial densities and, therefore, microbial community composition and function. These ecological interactions are likely to be greatly affected by evolutionary dynamics because bacteria can rapidly evolve resistance to phage, while phage can reciprocally evolve to increase infectivity. Most studies to date have explored eco-evolutionary dynamics using isolated pairs of bacteria-phage, but in nature, multiple bacteria and phages coexist and (co)evolve simultaneously. How coevolution plays out in this context is poorly understood. Here, we examine how three coexisting soil bacteria (<i>Ochrobactrum</i> sp., <i>Pseudomonas</i> sp. and <i>Variovorax</i> sp.) interact and evolve with three species-specific bacteriophages over 8 weeks of experimental evolution, both as host-parasite pairs in isolation and as a mixed community. Across all species, phage resistance evolution was inhibited in polyculture, with the most pronounced effect on <i>Ochrobactrum</i>. Between bacteria-phage pairs, there were also substantial differences in the effect of phage on host densities and evolutionary dynamics, including whether pairs coevolved. Our results also indicate bacteria have a relative advantage over phage, with high rates of phage extinction and/or lower densities in polyculture. These contrasts emphasize the difficulty in generalizing findings from monoculture to polyculture and between model bacteria-phage pairs to wider systems. Future studies should consider how multiple bacteria and phage pairs interact simultaneously to better understand how coevolutionary dynamics happen in natural communities.</p>","PeriodicalId":49819,"journal":{"name":"Microbiology-Sgm","volume":"171 6","pages":""},"PeriodicalIF":2.6000,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12178565/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microbiology-Sgm","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1099/mic.0.001577","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Bacteriophages can be important drivers of bacterial densities and, therefore, microbial community composition and function. These ecological interactions are likely to be greatly affected by evolutionary dynamics because bacteria can rapidly evolve resistance to phage, while phage can reciprocally evolve to increase infectivity. Most studies to date have explored eco-evolutionary dynamics using isolated pairs of bacteria-phage, but in nature, multiple bacteria and phages coexist and (co)evolve simultaneously. How coevolution plays out in this context is poorly understood. Here, we examine how three coexisting soil bacteria (Ochrobactrum sp., Pseudomonas sp. and Variovorax sp.) interact and evolve with three species-specific bacteriophages over 8 weeks of experimental evolution, both as host-parasite pairs in isolation and as a mixed community. Across all species, phage resistance evolution was inhibited in polyculture, with the most pronounced effect on Ochrobactrum. Between bacteria-phage pairs, there were also substantial differences in the effect of phage on host densities and evolutionary dynamics, including whether pairs coevolved. Our results also indicate bacteria have a relative advantage over phage, with high rates of phage extinction and/or lower densities in polyculture. These contrasts emphasize the difficulty in generalizing findings from monoculture to polyculture and between model bacteria-phage pairs to wider systems. Future studies should consider how multiple bacteria and phage pairs interact simultaneously to better understand how coevolutionary dynamics happen in natural communities.

细菌-噬菌体(co)的进化在多个细菌-噬菌体对的合成群落中受到限制。
噬菌体可以是细菌密度和微生物群落组成和功能的重要驱动因素。这些生态相互作用很可能受到进化动力学的极大影响,因为细菌可以迅速进化出对噬菌体的抗性,而噬菌体可以相互进化以增加传染性。迄今为止,大多数研究都是利用孤立的细菌噬菌体对探索生态进化动力学,但在自然界中,多种细菌和噬菌体共存并同时(共同)进化。在这种情况下,共同进化是如何发挥作用的,人们知之甚少。在这里,我们研究了三种共存的土壤细菌(Ochrobactrum sp., Pseudomonas sp.和Variovorax sp.)如何在8周的实验进化中与三种物种特异性噬菌体相互作用和进化,既可以作为单独的宿主-寄生虫对,也可以作为混合群落。在所有物种中,混交培养抑制了噬菌体抗性进化,其中对Ochrobactrum的影响最为明显。在细菌-噬菌体对之间,噬菌体对宿主密度和进化动力学的影响也存在实质性差异,包括对是否共同进化。我们的研究结果还表明,细菌比噬菌体具有相对优势,在混养中噬菌体灭绝率高,密度低。这些对比强调了将研究结果从单一培养推广到复合培养以及从模式细菌噬菌体对推广到更广泛的系统的困难。未来的研究应该考虑多种细菌和噬菌体对如何同时相互作用,以更好地了解共同进化动力学如何在自然群落中发生。
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
Microbiology-Sgm
Microbiology-Sgm 生物-微生物学
CiteScore
4.60
自引率
7.10%
发文量
132
审稿时长
3.0 months
期刊介绍: We publish high-quality original research on bacteria, fungi, protists, archaea, algae, parasites and other microscopic life forms. Topics include but are not limited to: Antimicrobials and antimicrobial resistance Bacteriology and parasitology Biochemistry and biophysics Biofilms and biological systems Biotechnology and bioremediation Cell biology and signalling Chemical biology Cross-disciplinary work Ecology and environmental microbiology Food microbiology Genetics Host–microbe interactions Microbial methods and techniques Microscopy and imaging Omics, including genomics, proteomics and metabolomics Physiology and metabolism Systems biology and synthetic biology The microbiome.
×
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