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The adhesion capability of Staphylococcus aureus cells is heterogeneously distributed over the cell envelope

View ORCID ProfileChristian Spengler, Erik Maikranz, Bernhard Glatz, View ORCID ProfileMichael Andreas Klatt, Hannah Heintz, View ORCID ProfileMarkus Bischoff, View ORCID ProfileLudger Santen, Andreas Fery, View ORCID ProfileKarin Jacobs
doi: https://doi.org/10.1101/2021.01.05.425282
Christian Spengler
aExperimental Physics, Saarland University, Center for Biophysics, 66123 Saarbrücken, Germany
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Erik Maikranz
bTheoretical Physics, Saarland University, Center for Biophysics, 66123 Saarbrücken, Germany
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Bernhard Glatz
cInstitute of Physical Chemistry and Physics of Polymers, Leibniz Institute of Polymer Research, 01069 Dresden, Germany
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Michael Andreas Klatt
dDepartment of Physics, Princeton University, Jadwin Hall, Princeton, NJ 08544-0001, USA
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Hannah Heintz
aExperimental Physics, Saarland University, Center for Biophysics, 66123 Saarbrücken, Germany
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Markus Bischoff
eInsitute of Medical Microbiology and Hygiene, Saarland University, Center for Bio-physics, 66421 Homburg/Saar, Germany
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Ludger Santen
bTheoretical Physics, Saarland University, Center for Biophysics, 66123 Saarbrücken, Germany
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Andreas Fery
fPhysical Chemistry of Polymer Materials, Technical University Dresden, 01062 Dresden, Germany
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Karin Jacobs
aExperimental Physics, Saarland University, Center for Biophysics, 66123 Saarbrücken, Germany
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  • ORCID record for Karin Jacobs
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Abstract

Understanding and controlling microbial adhesion is an important biomedical problem. However, many properties of the adhesion process of bacteria are still unknown, for example the distribution of adhesive strength over the cell wall. While a patchy colloid model for adhesion has been developed recently for Gram-negative Escherichia coli cells, a comparable model for Grampositive cells is unknown. Here, we use single-cell force spectroscopy to measure the adhesion of Staphylococcus aureus at different positions on tailored surfaces. We find heterogeneous adhesion profiles with varying degrees of intensity. By comparing these results to simulations, we find that locally increased adhesion can be explained by several distinct spots of high adhesion capabilities, similar to the patchy colloid model. Only for the underlying profile without local adhesive spots simple geometric considerations are insufficient. Rather, strong angle-dependent molecule-substratum interactions are necessary to explain the bathtub-like adhesion profiles seen for Staphylococcus aureus on a sinusoidal surface. We discuss implications of our results for the development of new materials and the design and analysis of future studies.

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

  • † Electronic Supplementary Information (ESI) available: See DOI: 00.0000/00000000.

  • ↵¶ Max Planck School Matter to Life, 69120 Heidelberg, Germany

  • The theoretical model has been altered and detailed and experimental results have been re-interpreted, therefore one author (H. Heintz) is added.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted May 15, 2023.
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The adhesion capability of Staphylococcus aureus cells is heterogeneously distributed over the cell envelope
Christian Spengler, Erik Maikranz, Bernhard Glatz, Michael Andreas Klatt, Hannah Heintz, Markus Bischoff, Ludger Santen, Andreas Fery, Karin Jacobs
bioRxiv 2021.01.05.425282; doi: https://doi.org/10.1101/2021.01.05.425282
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The adhesion capability of Staphylococcus aureus cells is heterogeneously distributed over the cell envelope
Christian Spengler, Erik Maikranz, Bernhard Glatz, Michael Andreas Klatt, Hannah Heintz, Markus Bischoff, Ludger Santen, Andreas Fery, Karin Jacobs
bioRxiv 2021.01.05.425282; doi: https://doi.org/10.1101/2021.01.05.425282

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