The biofilm life cycle: expanding the conceptual model of biofilm formation
Bacterial biofilms are often defined as communities of surface-attached bacteria and are typically depicted with a classic mushroom-shaped structure characteristic of Pseudomonas aeruginosa. However, it has become evident that this is not how all biofilms develop, especially in vivo, in clinical and...
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| Veröffentlicht in: | Nature reviews. Microbiology Jg. 20; H. 10; S. 608 - 620 |
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| Hauptverfasser: | , , , , , , |
| Format: | Journal Article |
| Sprache: | Englisch |
| Veröffentlicht: |
England
Nature Publishing Group
01.10.2022
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| Schlagworte: | |
| ISSN: | 1740-1526, 1740-1534, 1740-1534 |
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| Abstract | Bacterial biofilms are often defined as communities of surface-attached bacteria and are typically depicted with a classic mushroom-shaped structure characteristic of Pseudomonas aeruginosa. However, it has become evident that this is not how all biofilms develop, especially in vivo, in clinical and industrial settings, and in the environment, where biofilms often are observed as non-surface-attached aggregates. In this Review, we describe the origin of the current five-step biofilm development model and why it fails to capture many aspects of bacterial biofilm physiology. We aim to present a simplistic developmental model for biofilm formation that is flexible enough to include all the diverse scenarios and microenvironments where biofilms are formed. With this new expanded, inclusive model, we hereby introduce a common platform for developing an understanding of biofilms and anti-biofilm strategies that can be tailored to the microenvironment under investigation. |
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| AbstractList | Bacterial biofilms are often defined as communities of surface-attached bacteria and are typically depicted with a classic mushroom-shaped structure characteristic of Pseudomonas aeruginosa. However, it has become evident that this is not how all biofilms develop, especially in vivo, in clinical and industrial settings, and in the environment, where biofilms often are observed as non-surface-attached aggregates. In this Review, we describe the origin of the current five-step biofilm development model and why it fails to capture many aspects of bacterial biofilm physiology. We aim to present a simplistic developmental model for biofilm formation that is flexible enough to include all the diverse scenarios and microenvironments where biofilms are formed. With this new expanded, inclusive model, we hereby introduce a common platform for developing an understanding of biofilms and anti-biofilm strategies that can be tailored to the microenvironment under investigation.Bacterial biofilms are often defined as communities of surface-attached bacteria and are typically depicted with a classic mushroom-shaped structure characteristic of Pseudomonas aeruginosa. However, it has become evident that this is not how all biofilms develop, especially in vivo, in clinical and industrial settings, and in the environment, where biofilms often are observed as non-surface-attached aggregates. In this Review, we describe the origin of the current five-step biofilm development model and why it fails to capture many aspects of bacterial biofilm physiology. We aim to present a simplistic developmental model for biofilm formation that is flexible enough to include all the diverse scenarios and microenvironments where biofilms are formed. With this new expanded, inclusive model, we hereby introduce a common platform for developing an understanding of biofilms and anti-biofilm strategies that can be tailored to the microenvironment under investigation. Bacterial biofilms are often defined as communities of surface-attached bacteria and are typically depicted with a classic mushroom-shaped structure characteristic of Pseudomonas aeruginosa. However, it has become evident that this is not how all biofilms develop, especially in vivo, in clinical and industrial settings, and in the environment, where biofilms often are observed as non-surface-attached aggregates. In this Review, we describe the origin of the current five-step biofilm development model and why it fails to capture many aspects of bacterial biofilm physiology. We aim to present a simplistic developmental model for biofilm formation that is flexible enough to include all the diverse scenarios and microenvironments where biofilms are formed. With this new expanded, inclusive model, we hereby introduce a common platform for developing an understanding of biofilms and anti-biofilm strategies that can be tailored to the microenvironment under investigation.In this Review, Bjarnsholt and colleagues propose a revised conceptual model of the biofilm life cycle that encompasses the three major steps of biofilm formation — aggregation, growth and disaggregation — independently of surfaces, and initiation from single-cell planktonic bacteria, and thus represents a broader range of biofilm systems. Bacterial biofilms are often defined as communities of surface-attached bacteria and are typically depicted with a classic mushroom-shaped structure characteristic of Pseudomonas aeruginosa. However, it has become evident that this is not how all biofilms develop, especially in vivo, in clinical and industrial settings, and in the environment, where biofilms often are observed as non-surface-attached aggregates. In this Review, we describe the origin of the current five-step biofilm development model and why it fails to capture many aspects of bacterial biofilm physiology. We aim to present a simplistic developmental model for biofilm formation that is flexible enough to include all the diverse scenarios and microenvironments where biofilms are formed. With this new expanded, inclusive model, we hereby introduce a common platform for developing an understanding of biofilms and anti-biofilm strategies that can be tailored to the microenvironment under investigation. |
| Author | Bjarnsholt, Thomas Stewart, Philip S Stoodley, Paul Goeres, Darla M Sauer, Karin Burmølle, Mette Hall-Stoodley, Luanne |
| Author_xml | – sequence: 1 givenname: Karin orcidid: 0000-0002-1177-6328 surname: Sauer fullname: Sauer, Karin organization: Binghamton Biofilm Research Center, Binghamton University, Binghamton, NY, USA – sequence: 2 givenname: Paul orcidid: 0000-0001-6069-273X surname: Stoodley fullname: Stoodley, Paul organization: National Biofilm Innovation Centre (NBIC) and National Centre for Advanced Tribology at Southampton (nCATS), Mechanical Engineering, University of Southampton, Southampton, UK – sequence: 3 givenname: Darla M orcidid: 0000-0002-6320-9616 surname: Goeres fullname: Goeres, Darla M organization: Department of Chemical and Biological Engineering and Center for Biofilm Engineering, Montana State University, Bozeman, MT, USA – sequence: 4 givenname: Luanne orcidid: 0000-0003-2531-4797 surname: Hall-Stoodley fullname: Hall-Stoodley, Luanne organization: Department of Microbial Infection and Immunity, College of Medicine, The Ohio State University, Columbus, OH, USA – sequence: 5 givenname: Mette orcidid: 0000-0003-1870-632X surname: Burmølle fullname: Burmølle, Mette organization: Department of Biology, Faculty of Science, University of Copenhagen, Copenhagen, Denmark – sequence: 6 givenname: Philip S orcidid: 0000-0001-7773-8570 surname: Stewart fullname: Stewart, Philip S organization: Department of Chemical and Biological Engineering and Center for Biofilm Engineering, Montana State University, Bozeman, MT, USA – sequence: 7 givenname: Thomas orcidid: 0000-0002-8003-7414 surname: Bjarnsholt fullname: Bjarnsholt, Thomas email: tbjarnsholt@sund.ku.dk, tbjarnsholt@sund.ku.dk organization: Department of Clinical Microbiology, Rigshospitalet, Copenhagen, Denmark. tbjarnsholt@sund.ku.dk |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/35922483$$D View this record in MEDLINE/PubMed |
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| ContentType | Journal Article |
| Copyright | 2022. Springer Nature Limited. Springer Nature Limited 2022. Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. |
| Copyright_xml | – notice: 2022. Springer Nature Limited. – notice: Springer Nature Limited 2022. Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. |
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| DOI | 10.1038/s41579-022-00767-0 |
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