密切相关的细菌物种间细胞伸长的表型可塑性

IF 15.7 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
Marie Delaby, Liu Yang, Maxime Jacq, Kelley A. Gallagher, David T. Kysela, Velocity Hughes, Francisco Pulido, Frederic J. Veyrier, Michael S. VanNieuwenhze, Yves V. Brun
{"title":"密切相关的细菌物种间细胞伸长的表型可塑性","authors":"Marie Delaby, Liu Yang, Maxime Jacq, Kelley A. Gallagher, David T. Kysela, Velocity Hughes, Francisco Pulido, Frederic J. Veyrier, Michael S. VanNieuwenhze, Yves V. Brun","doi":"10.1038/s41467-025-60005-y","DOIUrl":null,"url":null,"abstract":"<p>Cell elongation in bacteria has been studied over many decades, in part because its underlying mechanisms are targets of numerous antibiotics. While multiple elongation modes have been described, little is known about how these strategies vary across species and in response to evolutionary and environmental influences. Here, we use fluorescent D-amino acids to track the spatiotemporal dynamics of bacterial cell elongation, revealing unsuspected diversity of elongation modes among closely related species of the family <i>Caulobacteraceae</i>. We identify species-specific combinations of dispersed, midcell and polar elongation that can be either unidirectional or bidirectional. Using genetic, cell biology, and phylogenetic approaches, we demonstrate that evolution of unidirectional-midcell elongation is accompanied by changes in the localization of the peptidoglycan synthase PBP2. Our findings reveal high phenotypic plasticity in elongation mechanisms, with implications for our understanding of bacterial growth and evolution.</p>","PeriodicalId":19066,"journal":{"name":"Nature Communications","volume":"29 1","pages":""},"PeriodicalIF":15.7000,"publicationDate":"2025-06-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Phenotypic plasticity in cell elongation among closely related bacterial species\",\"authors\":\"Marie Delaby, Liu Yang, Maxime Jacq, Kelley A. Gallagher, David T. Kysela, Velocity Hughes, Francisco Pulido, Frederic J. Veyrier, Michael S. VanNieuwenhze, Yves V. Brun\",\"doi\":\"10.1038/s41467-025-60005-y\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Cell elongation in bacteria has been studied over many decades, in part because its underlying mechanisms are targets of numerous antibiotics. While multiple elongation modes have been described, little is known about how these strategies vary across species and in response to evolutionary and environmental influences. Here, we use fluorescent D-amino acids to track the spatiotemporal dynamics of bacterial cell elongation, revealing unsuspected diversity of elongation modes among closely related species of the family <i>Caulobacteraceae</i>. We identify species-specific combinations of dispersed, midcell and polar elongation that can be either unidirectional or bidirectional. Using genetic, cell biology, and phylogenetic approaches, we demonstrate that evolution of unidirectional-midcell elongation is accompanied by changes in the localization of the peptidoglycan synthase PBP2. Our findings reveal high phenotypic plasticity in elongation mechanisms, with implications for our understanding of bacterial growth and evolution.</p>\",\"PeriodicalId\":19066,\"journal\":{\"name\":\"Nature Communications\",\"volume\":\"29 1\",\"pages\":\"\"},\"PeriodicalIF\":15.7000,\"publicationDate\":\"2025-06-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nature Communications\",\"FirstCategoryId\":\"103\",\"ListUrlMain\":\"https://doi.org/10.1038/s41467-025-60005-y\",\"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}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature Communications","FirstCategoryId":"103","ListUrlMain":"https://doi.org/10.1038/s41467-025-60005-y","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

摘要

细菌的细胞伸长已经研究了几十年,部分原因是它的潜在机制是许多抗生素的目标。虽然已经描述了多种伸长模式,但对这些策略在不同物种之间以及对进化和环境影响的响应如何变化知之甚少。在这里,我们使用荧光d -氨基酸来跟踪细菌细胞伸长的时空动态,揭示了在密切相关的根杆菌科物种之间的伸长模式的出乎意料的多样性。我们确定了分散,中细胞和极性延伸的物种特异性组合,可以是单向或双向的。利用遗传学、细胞生物学和系统发育方法,我们证明了单向中细胞延伸的进化伴随着肽聚糖合成酶PBP2定位的变化。我们的研究结果揭示了延伸机制的高表型可塑性,这对我们理解细菌的生长和进化具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Phenotypic plasticity in cell elongation among closely related bacterial species

Phenotypic plasticity in cell elongation among closely related bacterial species

Cell elongation in bacteria has been studied over many decades, in part because its underlying mechanisms are targets of numerous antibiotics. While multiple elongation modes have been described, little is known about how these strategies vary across species and in response to evolutionary and environmental influences. Here, we use fluorescent D-amino acids to track the spatiotemporal dynamics of bacterial cell elongation, revealing unsuspected diversity of elongation modes among closely related species of the family Caulobacteraceae. We identify species-specific combinations of dispersed, midcell and polar elongation that can be either unidirectional or bidirectional. Using genetic, cell biology, and phylogenetic approaches, we demonstrate that evolution of unidirectional-midcell elongation is accompanied by changes in the localization of the peptidoglycan synthase PBP2. Our findings reveal high phenotypic plasticity in elongation mechanisms, with implications for our understanding of bacterial growth and evolution.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Nature Communications
Nature Communications Biological Science Disciplines-
CiteScore
24.90
自引率
2.40%
发文量
6928
审稿时长
3.7 months
期刊介绍: Nature Communications, an open-access journal, publishes high-quality research spanning all areas of the natural sciences. Papers featured in the journal showcase significant advances relevant to specialists in each respective field. With a 2-year impact factor of 16.6 (2022) and a median time of 8 days from submission to the first editorial decision, Nature Communications is committed to rapid dissemination of research findings. As a multidisciplinary journal, it welcomes contributions from biological, health, physical, chemical, Earth, social, mathematical, applied, and engineering sciences, aiming to highlight important breakthroughs within each domain.
×
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