Dynamics of bacterial biofilm development imaged using light sheet fluorescence microscopy.

IF 2.2 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Biochemistry and Biophysics Reports Pub Date : 2025-08-16 eCollection Date: 2025-09-01 DOI:10.1016/j.bbrep.2025.102127
Lenka Šmerdová, Tibor Füzik, Lucie Valentová, Pavol Bárdy, Michaela Procházková, Martina Pařenicová, Pavel Plevka
{"title":"Dynamics of bacterial biofilm development imaged using light sheet fluorescence microscopy.","authors":"Lenka Šmerdová, Tibor Füzik, Lucie Valentová, Pavol Bárdy, Michaela Procházková, Martina Pařenicová, Pavel Plevka","doi":"10.1016/j.bbrep.2025.102127","DOIUrl":null,"url":null,"abstract":"<p><p>Biofilm formation exacerbates bacterial infections and interferes with industrial processes. However, the dynamics of biofilm development, especially if formed by a combination of more than one species, is not entirely understood. Here, we present a microfluidic cultivation system that enables continuous imaging of biofilm growth using light sheet fluorescence microscopy (LSFM). We studied the development of biofilms of the human pathogens <i>Staphylococcus aureus</i> and <i>Pseudomonas aeruginosa</i>. Multidirectional LSFM imaging enables the calculation of a three-dimensional reconstruction of the biofilm structure with isotropic resolution. Whereas <i>S. aureus</i> forms 50-70-μm-thick mushroom-like structures, a <i>P. aeruginosa</i> biofilm is 10-15 μm thick with cell clusters 25 μm in diameter. A combined biofilm resulted in the formation of large mushroom-like clusters of <i>S. aureus</i> cells that were subsequently dispersed by invading <i>P. aeruginosa.</i> A higher inoculation ratio favoring <i>P. aeruginosa</i> resulted in the formation of small and stable <i>S. aureus</i> clusters overgrown with <i>P. aeruginosa</i> cells. Applying conditioned media from <i>S. aureus</i> and <i>P. aeruginosa</i> coculture to a single-species <i>S. aureus</i> biofilm induced its dispersion. Integrating a microfluidic system into LSFM enables the visualization of biofilm formation dynamics and the effects of compounds on biofilm development.</p>","PeriodicalId":8771,"journal":{"name":"Biochemistry and Biophysics Reports","volume":"43 ","pages":"102127"},"PeriodicalIF":2.2000,"publicationDate":"2025-08-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12390859/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biochemistry and Biophysics Reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.bbrep.2025.102127","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/9/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Biofilm formation exacerbates bacterial infections and interferes with industrial processes. However, the dynamics of biofilm development, especially if formed by a combination of more than one species, is not entirely understood. Here, we present a microfluidic cultivation system that enables continuous imaging of biofilm growth using light sheet fluorescence microscopy (LSFM). We studied the development of biofilms of the human pathogens Staphylococcus aureus and Pseudomonas aeruginosa. Multidirectional LSFM imaging enables the calculation of a three-dimensional reconstruction of the biofilm structure with isotropic resolution. Whereas S. aureus forms 50-70-μm-thick mushroom-like structures, a P. aeruginosa biofilm is 10-15 μm thick with cell clusters 25 μm in diameter. A combined biofilm resulted in the formation of large mushroom-like clusters of S. aureus cells that were subsequently dispersed by invading P. aeruginosa. A higher inoculation ratio favoring P. aeruginosa resulted in the formation of small and stable S. aureus clusters overgrown with P. aeruginosa cells. Applying conditioned media from S. aureus and P. aeruginosa coculture to a single-species S. aureus biofilm induced its dispersion. Integrating a microfluidic system into LSFM enables the visualization of biofilm formation dynamics and the effects of compounds on biofilm development.

利用薄片荧光显微镜成像细菌生物膜发育的动态。
生物膜的形成加剧了细菌感染并干扰了工业过程。然而,生物膜发育的动力学,特别是由多个物种的组合形成的生物膜,还没有完全被理解。在这里,我们提出了一种微流体培养系统,可以使用光片荧光显微镜(LSFM)对生物膜生长进行连续成像。对人类病原菌金黄色葡萄球菌和铜绿假单胞菌的生物膜发育进行了研究。多向LSFM成像能够计算出具有各向同性分辨率的生物膜结构的三维重建。金黄色葡萄球菌形成50-70 μm厚的蘑菇状结构,铜绿假单胞菌形成10-15 μm厚的细胞团,直径为25 μm。结合的生物膜导致金黄色葡萄球菌细胞形成大型蘑菇状簇,随后被入侵的铜绿假单胞菌分散。较高的接种比例有利于铜绿假单胞菌的形成,导致小而稳定的金黄色葡萄球菌簇被铜绿假单胞菌细胞覆盖。将金黄色葡萄球菌和铜绿假单胞菌共培养的条件培养基用于单种金黄色葡萄球菌生物膜诱导其分散。将微流控系统集成到LSFM中,可以可视化生物膜形成动力学和化合物对生物膜发育的影响。
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
Biochemistry and Biophysics Reports
Biochemistry and Biophysics Reports Biochemistry, Genetics and Molecular Biology-Biophysics
CiteScore
4.60
自引率
0.00%
发文量
191
审稿时长
59 days
期刊介绍: Open access, online only, peer-reviewed international journal in the Life Sciences, established in 2014 Biochemistry and Biophysics Reports (BB Reports) publishes original research in all aspects of Biochemistry, Biophysics and related areas like Molecular and Cell Biology. BB Reports welcomes solid though more preliminary, descriptive and small scale results if they have the potential to stimulate and/or contribute to future research, leading to new insights or hypothesis. Primary criteria for acceptance is that the work is original, scientifically and technically sound and provides valuable knowledge to life sciences research. We strongly believe all results deserve to be published and documented for the advancement of science. BB Reports specifically appreciates receiving reports on: Negative results, Replication studies, Reanalysis of previous datasets.
×
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