Taurolidine Acts on Bacterial Virulence Factors and Does Not Induce Resistance in Periodontitis-Associated Bacteria-An In-Vitro Study

• Published in: Antibiotics (Basel) Vol. 9; no. 4; p. 166
• Main Authors: Radakovic, Sabrina, Andreoli, Nicola, Schmid, Simon, Nietzsche, Sandor, Zumbrunn, Jürg, Sculean, Anton, Eick, Sigrun
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 07-04-2020; MDPI
• Subjects: Anti-infective agents; development of resistance; Dosage and administration; Drug therapy; mechanisms of action; Microbial drug resistance; minocycline; Observations; Patient outcomes; periodontal pathogens; Periodontitis; taurolidine; Virulence (Microbiology); Germany; taurolidine; periodontal pathogens; minocycline; development of resistance; mechanisms of action
• ISSN: 2079-6382; 2079-6382
• DOI: 10.3390/antibiotics9040166

The aims of the present study were: (a) to determine the mechanism of action of taurolidine against bacterial species associated with periodontal disease, and (b) to evaluate the potential development of resistance against taurolidine as compared with minocycline. After visualizing the mode of action of taurolidine by transmission electron micrographs, the interaction with most important virulence factors (lipopolysaccharide (LPS),
gingipains,
leukotoxin), was analyzed. Then, 14 clinical isolates from subgingival biofilm samples were transferred on agar plates containing subinhibitory concentrations of taurolidine or minocycline up to 50 passages. Before and after each 10 passages, minimal inhibitory concentrations (MICs) were determined. Increasing MICs were screened for efflux mechanism. Taurolidine inhibited in a concentration-dependent manner the activities of LPS and of the arginine-specific gingipains; however, an effect on
leukotoxin was not detected. One
strain developed a resistance against taurolidine, which was probably linked with efflux
. An increase of MIC values of minocycline occurred in five of the 14 included strains after exposure to subinhibitory concentrations of the antibiotic. The present results indicate that: a) taurolidine interacts with LPS and gingipains, and b) development of resistance seems to be a rare event when using taurolidine.