Effect of a bacterial glutaminyl cyclase inhibitor on multi-species-biofilms

In all biofilms, total bacterial counts and those of <i>Pg</i> and <i>Tf</i> remained unaffected by the inhibitor. In the 12-species biofilm, both biomass and total metabolic activity decreased at high inhibitor concentrations (500 µM to 75.2 ± 6.5% and 87.2 ± 5.8%, respectively; each <i>p</i> < 0.001). The arginine-specific amidolytic activities of Rgp declined dose-dependently, down to 60.4 ± 10.2% (<i>p</i> < 0.001) at 500 µM of the inhibitor. Consequently, <i>Pg</i> colonies lost pigmentation as inhibitor concentrations increased. The inhibitor also reduced IL-1β release from monocytic cells stimulated by the 12-species biofilm. The studied [4,5-c]pyridine-based inhibitor is able to modify virulence of a multispecies biofilm. It might have the potential to be a promising approach in periodontal prevention and therapy.

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Publication Details

Journal
Frontiers in Oral Health
Published
2025-12-01
DOI
https://doi.org/10.3389/froh.2025.1716625
Citations
1
Primary Topic
Oral microbiology and periodontitis research
Type
article
Field-Weighted Citation Impact
1.47

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article

Effect of a bacterial glutaminyl cyclase inhibitor on multi-species-biofilms

Sigrun Eick, Mirko Buchholz, Daniel Ramsbeck, Nadine Taudte et al.
1 citations
Frontiers in Oral Health
Oral microbiology and periodontitis research
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article

Effect of a bacterial glutaminyl cyclase inhibitor on multi-species-biofilms

Sigrun Eick, Mirko Buchholz, Daniel Ramsbeck, Nadine Taudte, Jan Potempa, Anna Magdoń, Anton Sculean
article en
1 citations

Abstract

In all biofilms, total bacterial counts and those of <i>Pg</i> and <i>Tf</i> remained unaffected by the inhibitor. In the 12-species biofilm, both biomass and total metabolic activity decreased at high inhibitor concentrations (500 µM to 75.2 ± 6.5% and 87.2 ± 5.8%, respectively; each <i>p</i> < 0.001). The arginine-specific amidolytic activities of Rgp declined dose-dependently, down to 60.4 ± 10.2% (<i>p</i> < 0.001) at 500 µM of the inhibitor. Consequently, <i>Pg</i> colonies lost pigmentation as inhibitor concentrations increased. The inhibitor also reduced IL-1β release from monocytic cells stimulated by the 12-species biofilm. The studied [4,5-c]pyridine-based inhibitor is able to modify virulence of a multispecies biofilm. It might have the potential to be a promising approach in periodontal prevention and therapy.

Frontiers in Oral HealthVol. 6
University of Bern (CH), Jagiellonian University (PL), University of Louisville (US), Leibniz Institute of Plant Biochemistry (DE), Fraunhofer Institute for Cell Therapy and Immunology (DE)
Bundesministerium für Bildung und Forschung
Openalex Percentile: Top 13%
Oral microbiology and periodontitis research
1.47
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