Please use this identifier to cite or link to this item: doi:10.22028/D291-42022
Title: The adhesion capability of Staphylococcus aureus cells is heterogeneously distributed over the cell envelope
Author(s): Spengler, Christian
Maikranz, Erik
Glatz, Bernhard
Klatt, Michael Andreas
Heintz, Hannah
Bischoff, Markus
Santen, Ludger
Fery, Andreas
Jacobs, Karin
Language: English
Title: Soft Matter
Volume: 20 (2024)
Issue: 3
Pages: 484-494
Publisher/Platform: Royal Society of Chemistry
Year of Publication: 2023
DDC notations: 500 Science
610 Medicine and health
Publikation type: Journal Article
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 of the first publication: 10.1039/D3SM01045G
URL of the first publication: https://doi.org/10.1039/D3SM01045G
Link to this record: 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
Date of registration: 7-May-2024
Description of the related object: Electronic supplementary information
Related object: https://www.rsc.org/suppdata/d3/sm/d3sm01045g/d3sm01045g1.pdf
Faculty: M - Medizinische Fakultät
NT - Naturwissenschaftlich- Technische Fakultät
Department: M - Infektionsmedizin
NT - Physik
Professorship: M - Prof. Dr. Sören Becker
NT - Prof. Dr. Karin Jacobs
NT - Prof. Dr. Ludger Santen
Collections:SciDok - Der Wissenschaftsserver der Universität des Saarlandes

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