An anaerobic in vitro flow model for studying interactions at the gastrointestinal host-microbe interface.

IF 9.2 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
L L Bang, J S Pettersen, N Høiland, A M Rojek, D R Tornby, J Møller-Jensen, U S Justesen, R M Pedersen, T E Andersen
{"title":"An anaerobic in vitro flow model for studying interactions at the gastrointestinal host-microbe interface.","authors":"L L Bang, J S Pettersen, N Høiland, A M Rojek, D R Tornby, J Møller-Jensen, U S Justesen, R M Pedersen, T E Andersen","doi":"10.1038/s41522-025-00800-z","DOIUrl":null,"url":null,"abstract":"<p><p>In vitro research on host-microbe interactions in the human gut has been challenging due to the differing oxygen requirements of mammalian cells and intestinal microbiota. Few models of this environment have been developed, and those available are complex, limiting the extraction of important information during experiments. Here we report an in vitro model that by simple means creates an anaerobic environment for microbiota growing on living, cultured human epithelium under physiological flow. This model enables long-term co-culture of intestinal epithelial cells with obligate anaerobic bacteria, exemplified here by Clostridioides difficile and Bacteroides fragilis. Anaerobic conditions are maintained through the integration of an anaerobization unit, developed to facilitate online deoxygenation of media via liquid-to-liquid gas diffusion, eliminating the need for encapsulation in complex gas chambers. We show that stable oxygen levels of less than 1% can be maintained in the model for several days without compromising the viability of the intestinal epithelium. Furthermore, we demonstrate the performance of the model by simulating prolonged colonization with C. difficile and B. fragilis, as well as the clinically relevant persistence of C. difficile following treatment with vancomycin.</p>","PeriodicalId":19370,"journal":{"name":"npj Biofilms and Microbiomes","volume":"11 1","pages":"160"},"PeriodicalIF":9.2000,"publicationDate":"2025-08-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12340051/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"npj Biofilms and Microbiomes","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1038/s41522-025-00800-z","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

In vitro research on host-microbe interactions in the human gut has been challenging due to the differing oxygen requirements of mammalian cells and intestinal microbiota. Few models of this environment have been developed, and those available are complex, limiting the extraction of important information during experiments. Here we report an in vitro model that by simple means creates an anaerobic environment for microbiota growing on living, cultured human epithelium under physiological flow. This model enables long-term co-culture of intestinal epithelial cells with obligate anaerobic bacteria, exemplified here by Clostridioides difficile and Bacteroides fragilis. Anaerobic conditions are maintained through the integration of an anaerobization unit, developed to facilitate online deoxygenation of media via liquid-to-liquid gas diffusion, eliminating the need for encapsulation in complex gas chambers. We show that stable oxygen levels of less than 1% can be maintained in the model for several days without compromising the viability of the intestinal epithelium. Furthermore, we demonstrate the performance of the model by simulating prolonged colonization with C. difficile and B. fragilis, as well as the clinically relevant persistence of C. difficile following treatment with vancomycin.

用于研究胃肠道宿主-微生物界面相互作用的体外厌氧流动模型。
由于哺乳动物细胞和肠道微生物群对氧气的需求不同,在体外研究人类肠道中宿主-微生物相互作用一直具有挑战性。这种环境的模型很少,而且可用的模型很复杂,限制了实验中重要信息的提取。在这里,我们报告了一个体外模型,通过简单的方法为微生物群在生理流动下在活的培养的人上皮上生长创造了一个厌氧环境。该模型可以使肠上皮细胞与专性厌氧细菌长期共同培养,例如艰难梭菌和脆弱拟杆菌。厌氧条件通过厌氧装置的集成来维持,厌氧装置的开发是为了通过液-液气体扩散促进介质的在线脱氧,从而消除了在复杂的毒气室中封装的需要。我们发现,低于1%的稳定氧水平可以在模型中维持数天,而不会损害肠上皮的活力。此外,我们通过模拟艰难梭菌和脆弱芽孢杆菌的长时间定植以及万古霉素治疗后艰难梭菌的临床持久性来证明该模型的性能。
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
npj Biofilms and Microbiomes
npj Biofilms and Microbiomes Immunology and Microbiology-Microbiology
CiteScore
12.10
自引率
3.30%
发文量
91
审稿时长
9 weeks
期刊介绍: npj Biofilms and Microbiomes is a comprehensive platform that promotes research on biofilms and microbiomes across various scientific disciplines. The journal facilitates cross-disciplinary discussions to enhance our understanding of the biology, ecology, and communal functions of biofilms, populations, and communities. It also focuses on applications in the medical, environmental, and engineering domains. The scope of the journal encompasses all aspects of the field, ranging from cell-cell communication and single cell interactions to the microbiomes of humans, animals, plants, and natural and built environments. The journal also welcomes research on the virome, phageome, mycome, and fungome. It publishes both applied science and theoretical work. As an open access and interdisciplinary journal, its primary goal is to publish significant scientific advancements in microbial biofilms and microbiomes. The journal enables discussions that span multiple disciplines and contributes to our understanding of the social behavior of microbial biofilm populations and communities, and their impact on life, human health, and the environment.
×
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