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doi:10.22028/D291-42022
Titel: | The adhesion capability of Staphylococcus aureus cells is heterogeneously distributed over the cell envelope |
VerfasserIn: | Spengler, Christian Maikranz, Erik Glatz, Bernhard Klatt, Michael Andreas Heintz, Hannah Bischoff, Markus Santen, Ludger Fery, Andreas Jacobs, Karin |
Sprache: | Englisch |
Titel: | Soft Matter |
Bandnummer: | 20 (2024) |
Heft: | 3 |
Seiten: | 484-494 |
Verlag/Plattform: | Royal Society of Chemistry |
Erscheinungsjahr: | 2023 |
DDC-Sachgruppe: | 500 Naturwissenschaften 610 Medizin, Gesundheit |
Dokumenttyp: | Journalartikel / Zeitschriftenartikel |
Abstract: | Understanding and controlling microbial adhesion is a critical challenge in biomedical research, given the profound impact of bacterial infections on global health. Many facets of bacterial adhesion, including the distribution of adhesion forces across the cell wall, remain poorly understood. While a recent ‘patchy colloid’ model has shed light on adhesion in Gram-negative Escherichia coli cells, a corresponding model for Gram-positive cells has been elusive. In this study, we employ single cell force spectroscopy to investigate the adhesion force of Staphylococcus aureus. Normally, only one contact point of the entire bacterial surface is measured. However, by using a sine-shaped surface and recording forcedistance curves along a path perpendicular to the rippled structures, we can characterize almost a hemisphere of one and the same bacterium. This unique approach allows us to study a greater number of contact points between the bacterium and the surface compared to conventional flat substrata. Distributed over the bacterial surface, we identify sites of higher and lower adhesion, which we call ‘patchy adhesion’, reminiscent of the patchy colloid model. The experimental results show that only some cells exhibit particularly strong adhesion at certain locations. To gain a better understanding of these locations, a geometric model of the bacterial cell surface was created. The experimental results were best reproduced by a model that features a few (5-6) particularly strong adhesion sites (diameter about 250 nm) that are widely distributed over the cell surface. Within the simulated patches, the number of molecules or their individual adhesive strength is increased. A more detailed comparison shows that simple geometric considerations for interacting molecules are not sufficient, but rather strong angle-dependent molecule-substratum interactions are required. We discuss the implications of our results for the development of new materials and the design and analysis of future studies. |
DOI der Erstveröffentlichung: | 10.1039/D3SM01045G |
URL der Erstveröffentlichung: | https://doi.org/10.1039/D3SM01045G |
Link zu diesem Datensatz: | urn:nbn:de:bsz:291--ds-420229 hdl:20.500.11880/37598 http://dx.doi.org/10.22028/D291-42022 |
ISSN: | 1744-6848 1744-683X |
Datum des Eintrags: | 7-Mai-2024 |
Bezeichnung des in Beziehung stehenden Objekts: | Electronic supplementary information |
In Beziehung stehendes Objekt: | https://www.rsc.org/suppdata/d3/sm/d3sm01045g/d3sm01045g1.pdf |
Fakultät: | M - Medizinische Fakultät NT - Naturwissenschaftlich- Technische Fakultät |
Fachrichtung: | M - Infektionsmedizin NT - Physik |
Professur: | M - Prof. Dr. Sören Becker NT - Prof. Dr. Karin Jacobs NT - Prof. Dr. Ludger Santen |
Sammlung: | SciDok - Der Wissenschaftsserver der Universität des Saarlandes |
Dateien zu diesem Datensatz:
Datei | Beschreibung | Größe | Format | |
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d3sm01045g.pdf | 5,34 MB | Adobe PDF | Öffnen/Anzeigen |
Diese Ressource wurde unter folgender Copyright-Bestimmung veröffentlicht: Lizenz von Creative Commons