Development of antiseptic adaptation and cross-adapatation in selected oral pathogens in vitro

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作者
Tim Verspecht
Esteban Rodriguez Herrero
Ladan Khodaparast
Laleh Khodaparast
Nico Boon
Kristel Bernaerts
Marc Quirynen
Wim Teughels
机构
[1] University of Leuven (KU Leuven),Department of Oral Health Sciences
[2] VIB Center for Brain and Disease Research,Switch Laboratory
[3] University of Leuven (KU Leuven),Switch Laboratory, Department of Cellular and Molecular Medicine
[4] Ghent University (UGent),Center for Microbial Ecology and Technology (CMET)
[5] University of Leuven (KU Leuven),Bio
[6] Dentistry, and Chemical Systems Technology, Reactor Engineering and Safety, Department of Chemical Engineering
[7] University Hospitals Leuven,undefined
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There is evidence that pathogenic bacteria can adapt to antiseptics upon repeated exposure. More alarming is the concomitant increase in antibiotic resistance that has been described for some pathogens. Unfortunately, effects of adaptation and cross-adaptation are hardly known for oral pathogens, which are very frequently exposed to antiseptics. Therefore, this study aimed to determine the in vitro increase in minimum inhibitory concentrations (MICs) in oral pathogens after repeated exposure to chlorhexidine or cetylpyridinium chloride, to examine if (cross-)adaptation to antiseptics/antibiotics occurs, if (cross-)adaptation is reversible and what the potential underlying mechanisms are. When the pathogens were exposed to antiseptics, their MICs significantly increased. This increase was in general at least partially conserved after regrowth without antiseptics. Some of the adapted species also showed cross-adaptation, as shown by increased MICs of antibiotics and the other antiseptic. In most antiseptic-adapted bacteria, cell-surface hydrophobicity was increased and mass-spectrometry analysis revealed changes in expression of proteins involved in a wide range of functional domains. These in vitro data shows the adaptation and cross-adaptation of oral pathogens to antiseptics and antibiotics. This was related to changes in cell surface hydrophobicity and in expression of proteins involved in membrane transport, virulence, oxidative stress protection and metabolism.
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