Impact of Exposure of Methicillin-Resistant Staphylococcus aureus to Polyhexanide In Vitro and In Vivo
Autor: | Jacques Schrenzel, Abdessalam Cherkaoui, Alex J. O'Neill, Patrice Francois, Caroline Landelle, A. S. Bayer, Adriana Renzoni, Damien Baud, Stéphan Juergen Harbarth, E. von Dach, Seydina M. Diene, E-J Bonetti, Christopher P. Randall, R. Gonzales, Wessam Abdelhady, Caroline Manzano |
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Přispěvatelé: | Techniques pour l'Evaluation et la Modélisation des Actions de la Santé (TIMC-IMAG-ThEMAS), Techniques de l'Ingénierie Médicale et de la Complexité - Informatique, Mathématiques et Applications, Grenoble - UMR 5525 (TIMC-IMAG), Institut polytechnique de Grenoble - Grenoble Institute of Technology (Grenoble INP )-VetAgro Sup - Institut national d'enseignement supérieur et de recherche en alimentation, santé animale, sciences agronomiques et de l'environnement (VAS)-Centre National de la Recherche Scientifique (CNRS)-Université Grenoble Alpes [2016-2019] (UGA [2016-2019])-Institut polytechnique de Grenoble - Grenoble Institute of Technology (Grenoble INP )-VetAgro Sup - Institut national d'enseignement supérieur et de recherche en alimentation, santé animale, sciences agronomiques et de l'environnement (VAS)-Centre National de la Recherche Scientifique (CNRS)-Université Grenoble Alpes [2016-2019] (UGA [2016-2019]), Centre Hospitalier Universitaire [Grenoble] (CHU), Laboratory of Genetics (UPV ⁄ EHU), University of the Basque Country/Euskal Herriko Unibertsitatea (UPV/EHU), Instituto de Ciencias Nucleares [Mexico], Universidad Nacional Autónoma de México (UNAM), Laboratory for Atmospheric and Space Physics [Boulder] (LASP), University of Colorado [Boulder], Institute of Environmental Physics [Heidelberg] (IUP), Universität Heidelberg [Heidelberg], Laboratoire Hubert Curien [Saint Etienne] (LHC), Institut d'Optique Graduate School (IOGS)-Université Jean Monnet [Saint-Étienne] (UJM)-Centre National de la Recherche Scientifique (CNRS), Service infectious diseases, Hôpitaux Universitaires de Genève (HUG), Prévention et contrôle des infections (PCI ) |
Jazyk: | angličtina |
Rok vydání: | 2017 |
Předmět: |
0301 basic medicine
Methicillin-Resistant Staphylococcus aureus medicine.drug_class [SDV]Life Sciences [q-bio] 030106 microbiology Antibiotics Polyhexanide Biguanides Mupirocin Microbial Sensitivity Tests medicine.disease_cause Microbiology Epidemiology and Surveillance 03 medical and health sciences chemistry.chemical_compound Antiseptic Bacterial Proteins Daptomycin Cell Wall Drug Resistance Bacterial medicine Humans Pharmacology (medical) ComputingMilieux_MISCELLANEOUS Pharmacology ddc:616 business.industry Chlorhexidine High-Throughput Nucleotide Sequencing Staphylococcal Infections Aminoacyltransferases Methicillin-resistant Staphylococcus aureus 3. Good health Anti-Bacterial Agents Repressor Proteins 030104 developmental biology Infectious Diseases chemistry Staphylococcus aureus Anti-Infective Agents Local [SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie business medicine.drug |
Zdroj: | Antimicrobial Agents and Chemotherapy Antimicrobial Agents and Chemotherapy, American Society for Microbiology, 2017, 61 (10) Antimicrobial Agents and Chemotherapy, Vol. 61, No 10 (2017) pp. e00272-17 |
ISSN: | 0066-4804 1098-6596 |
Popis: | Methicillin-resistant Staphylococcus aureus (MRSA) resistant to decolonization agents such as mupirocin and chlorhexidine increases the need for development of alternative decolonization molecules. The absence of reported severe adverse reactions and bacterial resistance to polyhexanide makes it an excellent choice as a topical antiseptic. In the present study, we evaluated the in vitro and in vivo capacity to generate strains with reduced polyhexanide susceptibility and cross-resistance with chlorhexidine and/or antibiotics currently used in clinic. Here we report the in vitro emergence of reduced susceptibility to polyhexanide by prolonged stepwise exposure to low concentrations in broth culture. Reduced susceptibility to polyhexanide was associated with genomic changes in the mprF and purR genes and with concomitant decreased susceptibility to daptomycin and other cell wall-active antibiotics. However, the in vitro emergence of reduced susceptibility to polyhexanide did not result in cross-resistance to chlorhexidine. During in vivo polyhexanide clinical decolonization treatment, neither reduced polyhexanide susceptibility nor chlorhexidine cross-resistance was observed. Together, these observations suggest that polyhexanide could be used safely for decolonization of carriers of chlorhexidine-resistant S. aureus strains; they also highlight the need for careful use of polyhexanide at low antiseptic concentrations. |
Databáze: | OpenAIRE |
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