Microbiological tests of materials platform

Project E

S. aureus visualized by immunolabelling of protein A (STED image) & S. aureus agar plate, generated by AI (Duck.ai)

Image: Pia Pritzke
S. aureus visualized by immunolabelling of protein A (STED image) & S. aureus agar plate, generated by AI (Duck.ai)

Project E combines microbiological testing with advanced fluorescence microscopy to study bacterial adhesion, biofilm formation, and cellular responses on novel biomaterials. The project establishes standardised workflows that allow materials developed across the RTG to be compared quantitatively and under reproducible experimental conditions.

Project E acts as a central microbiology and microscopy platform within the RTG Materials–Microbes–Microenvironments. The project establishes sensitive, reproducible, and quantitative workflows to evaluate microbial adhesion, biofilm formation, and material–cell interactions on novel antimicrobial and bioactive surfaces. Classical in vitro assays are used to compare bacterial attachment, growth, viability, and biofilm development on different material classes. These approaches provide reference data for materials developed in the other RTG projects and help identify surfaces with anti-adhesive or antimicrobial properties. In parallel, the microscopy branch develops and applies advanced fluorescence-based readouts, including widefield and confocal microscopy, STED microscopy, fluorescence correlation spectroscopy, GP imaging, and adaptive optics-supported approaches. Together, these methods bridge material development, microbiological testing, and optical technology development, enabling a standardised comparison of diverse biomaterial systems.

Research Highlights

Highlight 1: Tailored bioactive glass compositions reduce bacterial adhesion

Bioactive glass compositions with reduced silicon dioxide (SiO₂) content demonstrated pronounced anti-adhesive and antibacterial properties against multiple clinically relevant bacterial species. In addition, these materials showed synergistic effects when combined with conventional antibiotics, highlighting their potential as functional additives for orthopedic bone cements aimed at preventing implant-associated infections.

In contrast, glass compositions containing metallic additives exhibited lower overall efficacy and more species-specific antimicrobial activity. Among the tested components, calcium oxide (CaO) displayed a modest but reproducible inhibitory effect against Staphylococcus aureus. These findings suggest that combining a reduced SiO₂ content with optimized CaO concentrations may further enhance the anti-infective performance of bioactive glass materials.

Overall, the results support the development of tailored glass compositions as multifunctional biomaterials that not only improve implant integration but also contribute to reducing the risk of orthopedic implant-associated infections.

A. Bioactive glass: The lower the SiO2 content, the higher the antimicrobial activity against S. aureus. B. Bioactive glass shows synergy with antimicrobials used for orthopedic surgery and bone infections as systemic prophylaxis and localized delivery. C. Non-degradable glass with bioactive metal cations: Ca-oxide seems to have an effect on the attachment of S. aureus on the glass, while Zn-oxid shows no significant activity. K. pnuemonie is generally non-susiptible to both glass compsitions. QG: quartz glass, SLS: soda-lime silicate glass, Diameter: 315-500 µm.

Image: PD Dr. Oliwia Makarewicz

Highlight 2: Visualising microbial and cellular responses across biomaterial interfaces

Project E combines microbiological assays with complementary fluorescence microscopy techniques to visualise how different biomaterials influence bacterial adhesion, biofilm formation, and host-cell responses. Rather than focusing on a single model system, the project applies tailored imaging strategies to a wide range of materials and biological questions, enabling direct comparison across the RTG.

Examples include the imaging of osteoblast interactions with HSA nanofiber-coated surfaces, live/dead analysis of bacterial colonisation on titanium discs, the visualisation of osteoblast responses to bioactive glass treatment, and fluorescence imaging of Staphylococcus aureus biofilm formation on bioactive glass cylinders. Together, these experiments illustrate how Project E links microbiology and advanced optical microscopy to generate biologically meaningful and visually intuitive readouts for diverse biomaterial systems.

Representative fluorescence microscopy images illustrating the range of biological model systems and material surfaces investigated in Project E. A: Osteoblasts on HSA nanofibers. B: Live/dead staining of S.aureus on titanium discs. C: Osteoblasts treated with bioactive glass for 5 h. D: FRFP-expressing S. aureus biofilm formation after 24 h on a bioactive glass cylinder.

Image: Julius Trautmann

Related Publications

Alvelid, J., Koerfer, A., and Eggeling, C. (2026)
Smart event-triggered MINFLUX microscopy to catch and follow rare events
Nat. Commun. 17, 4558. https://doi.org/10.1038/s41467-026-73176-zExternal linkExternal link

Mirza, K.A., Nietzsche, S., Tchatchiashvili, T., Makarewicz, O., Pletz, M.W., and Thieme, L. (2025)
Implant-associated biofilms of Staphylococcus aureus and Enterococcus faecalis clinical isolates on expanded polytetrafluoroethylene suture in Galleria mellonella model
Sci. Rep. 15, 39555. https://doi.org/10.1038/s41598-025-26971-5External linkExternal link

Koceva, H., Amiratasgani, M., Akbarimoghaddam, P., Hoffmann, B., Zhurgenbayeva, G., Gresnigt, M-S., Marcelino, V.R., Eggeling, C., Figge, M.T., Amorim, M.-J., and Mosig, A.S. (2025)
Deciphering respiratory viral infections by harnessing organ-on-chip technology to explore the gut-lung axis
Open Biol. 15, 240231. https://doi.org/10.1098/rsob.240231External linkExternal link

Vogler, B.T.L., De Angelis, G., Zhao, Z., Eggeling; C., and Reina, F. (2025)
Parameter optimization for MINFLUX microscopy enabled single particle tracking
Commun. Biol. 8, 1573. https://doi.org/10.1038/s42003-025-09060-1External linkExternal link

Project Team

Prof. Dr. Christian Eggeling
Friedrich Schiller University Jena · Superresolution Microscopy
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Prof. Dr. Mathias Pletz
Jena University Hospital · Infectious Diseases and Infection ControlExternal link
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PD Dr. Oliwia Makarewicz
Jena University Hospital · Infectious Diseases and Infection ControlExternal link
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Helyaneh Moeinizadeh
Jena University Hospital · Infectious Diseases and Infection ControlExternal link
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Phuong Thanh Ngo
Jena University Hospital · Infectious Diseases and Infection ControlExternal link
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Pia Pritzke
Friedrich Schiller University Jena / Leibniz Institute of Photonic Technology · Biophysical ImagingExternal link
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Julius Trautmann
Friedrich Schiller University Jena · Superresolution Microscopy
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Dr. Micha Banz
Jena University Hospital · Infectious Diseases and Infection ControlExternal link
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Dr. Philine Fleckenstein
Jena University Hospital · Infectious Diseases and Infection ControlExternal link
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Dr. Kamran Mirza
Jena University Hospital · Infectious Diseases and Infection ControlExternal link
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Tinatini Tchatchiashvili
Jena University Hospital · Infectious Diseases and Infection ControlExternal link
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