News Release 

Why do hospital germs bind more strongly to certain surfaces than to others?

Saarland University

Research News


IMAGE: Model of the adhesion mechanism by which the bacterium Staphylococcus aureus binds to hydrophobic ('low-energy') surfaces (left) compared with hydrophilic ('high-energy') surfaces (right). On the left, a large number of... view more 

Credit: Saarland University

These results from studies in both experimental and theoretical physics may help to improve antibacterial surfaces. The research work was recently published in the journal 'Nanoscale'.

Staphylococcus aureus bacteria are one of the most common causes of infections acquired by patients during a stay in hospital. These pathogens are particularly problematic because they can form robust biofilms on both natural and artificial surfaces from which they are very difficult to remove. 'The individual bacteria within these biofilms are effectively protected from attack by antibiotics or by the human immune system. That's why it can be so dangerous when these bacteria colonize medical implants as they can then cause serious post-operative infections,' explains Karin Jacobs, Professor of Experimental Physics at Saarland University. It is therefore crucial to try and prevent these biofilms from forming in the first place.

However, to be able to influence biofilm growth, the researchers had to understand the mechanisms by which the bacteria adhere to different materials. Using a scanning atomic force microscope, they pressed the minute bacterial cells onto different types of surfaces and then determined the force needed to lift the adhered cells from the surface. This experimental configuration allowed the researchers to record what are known as force-distance curves. 'We used extremely smooth silicon surfaces as model surfaces. In one set of experiments, the silicon surfaces were prepared so that they had high water-wettability; in another set of experiments they were treated to be highly hydrophobic. We were able to show that the bacterial cells adhered far more strongly to the hydrophobic surfaces, from which water simply rolled off, than on the hydrophilic (water-wettable) surfaces,' explains Karin Jacobs. But it is not just the magnitude of the forces that differ between the two surface types, so too do the shapes of the force-distance curves (see figure). 'On the hydrophobic surfaces, we see very smooth curves with a characteristic cup shape. On the hydrophilic surfaces, in contrast, we observe force-distance curves with a very jagged profile,' says Professor Jacobs.

In order to understand these results, the dynamics of these complex systems were modelled using Monte Carlo simulations that were carried out in the research group led by Professor Ludger Santen, Professor of Theoretical Physics at Saarland University. The model treats the bacterial cell as a rigid sphere and the molecules in the cell wall that tether the cell to the surface as minute springs. 'It turns out that in order to reproduce the experimental results, the role played by the random (stochastic) nature of the molecular binding process is more important than trying to increase the complexity of the model. We have now uncovered why the bacteria cells behave so differently on different types of surfaces. On hydrophobic surfaces, a large number of the cell wall proteins adhere to the surface, which results in a strong binding force and yields a smooth force-distance curve,' explains Ludger Santen. In contrast, on a hydrophilic surface, far fewer cell wall proteins are involved in tethering the bacterium to the surface. As a result, the bacteria are held less strongly on the surface and the shape of the force-distance curve is less uniform. 'The jagged shape of the curves that we see with hydrophilic surfaces is caused by a few individual cell wall molecules as they are pulled from the surface. Because fewer cell wall proteins are involved, the bacteria bind less strongly to hydrophilic surfaces,' says Erik Maikranz, who carried out the Monte Carlo simulations as part of his doctoral research work.

Due to the different shapes of the force-distance curves, the physicists suppose that on a hydrophilic surface fewer cell wall proteins are involved in the binding process because these molecules first have to overcome a potential barrier, which effectively reduces the number of protein macromolecules that can tether the cell to the surface. 'The potential barrier to adhesion on hydrophilic surfaces is relatively high, so only a few of the cell wall proteins are able to overcome this energy barrier in a particular time. On hydrophobic surfaces, however, the barrier is negligibly small, so that many cell wall proteins can adhere directly to the surface,' explains Dr. Christian Spengler, who performed the experiments in the study.


The research project was supported by the German Research Foundation (DFG) as part of a Collaborative Research Centre (CRC 1027: 'Physical modeling of non-equilibrium processes in biological systems'). Researchers in the fields of physics, medical science, bioinformatics, biology and chemistry collaborate within CRC 1027 to study the fundamental physical principles underlying biological processes.

Original publication:

E. Maikranz, C. Spengler, N. Thewes, A. Thewes, F. Nolle, M. Bischoff, L. Santen and K. Jacobs, 'Different binding mechanisms of Staphylococcus aureus to hydrophobic and hydrophilic surfaces'; Nanoscale (2020), DOI: 10.1039/d0nr03134h

Further information:

The accompanying graphic and press photographs are available for use with this press release. They can be downloaded free of charge at:

Questions can be addressed to:

Prof. Dr. Karin Jacobs and Dr. Christian Spengler
Department of Experimental Physics, Centre for Biophysics, Saarland University
Tel.: +49 (0)681 302-71788

Prof. Dr. Ludger Santen and M. Sc. Erik Maikranz
Department of Theoretical Physics, Centre for Biophysics, Saarland University
Tel.: +49 (0)681 302-57411

Note for radio journalists: Studio-quality telephone interviews can be conducted with researchers at Saarland University using broadcast audio IP codec technology (IP direct dial or via the ARD node 106813020001). Interview requests should be addressed to the university's Press and Public Relations Office (+49 (0)681 302-3610).

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