Publication: Antimicrobial activity of octenidine against multidrug-resistant Gram-negative pathogens.
dc.contributor.author | Alvarez-Marin, R | |
dc.contributor.author | Aires-de-Sousa, M | |
dc.contributor.author | Nordmann, P | |
dc.contributor.author | Kieffer, N | |
dc.contributor.author | Poirel, L | |
dc.date.accessioned | 2023-01-25T09:51:02Z | |
dc.date.available | 2023-01-25T09:51:02Z | |
dc.date.issued | 2017-08-19 | |
dc.description.abstract | Multidrug-resistant (MR) Gram-negative (GN) pathogens pose a major and growing threat for healthcare systems, as therapy of infections is often limited due to the lack of available systemic antibiotics. Well-tolerated antiseptics, such as octenidine dihydrochloride (OCT), may be a very useful tool in infection control to reduce the dissemination of MRGN. This study aimed to investigate the bactericidal activity of OCT against international epidemic clones of MRGN. A set of five different species (Escherichia coli, Klebsiella pneumoniae, Enterobacter cloacae, Acinetobacter baumannii, and Pseudomonas aeruginosa) was studied to prove OCT efficacy without organic load, under "clean conditions" (0.3 g/L albumin) and under "dirty conditions" (3 g/L albumin + 3 mL/L defibrinated sheep blood), according to an official test norm (EN13727). We used five clonally unrelated isolates per species, including a susceptible wild-type strain, and four MRGN isolates, corresponding to either the 3MRGN or 4MRGN definition of multidrug resistance. A contact time of 1 min was fully effective for all isolates by using different OCT concentrations (0.01% and 0.05%), with a bacterial reduction factor of >5 log10 systematically observed. Growth kinetics were determined with two different wild-type strains (A. baumannii and K. pneumoniae), proving a time-dependent efficacy of OCT. These results highlight that OCT may be extremely useful to eradicate emerging highly resistant Gram-negative pathogens associated with nosocomial infections. | |
dc.identifier.doi | 10.1007/s10096-017-3070-0 | |
dc.identifier.essn | 1435-4373 | |
dc.identifier.pmid | 28825186 | |
dc.identifier.unpaywallURL | http://doc.rero.ch/record/305745/files/nor_aao.pdf | |
dc.identifier.uri | http://hdl.handle.net/10668/11523 | |
dc.issue.number | 12 | |
dc.journal.title | European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology | |
dc.journal.titleabbreviation | Eur J Clin Microbiol Infect Dis | |
dc.language.iso | en | |
dc.organization | Hospital Universitario Virgen del Rocío | |
dc.organization | Hospital Universitario Virgen Macarena | |
dc.page.number | 2379-2383 | |
dc.pubmedtype | Journal Article | |
dc.rights.accessRights | open access | |
dc.subject.mesh | Anti-Bacterial Agents | |
dc.subject.mesh | Anti-Infective Agents | |
dc.subject.mesh | Dose-Response Relationship, Drug | |
dc.subject.mesh | Drug Resistance, Multiple, Bacterial | |
dc.subject.mesh | Gram-Negative Bacteria | |
dc.subject.mesh | Gram-Negative Bacterial Infections | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Imines | |
dc.subject.mesh | Microbial Sensitivity Tests | |
dc.subject.mesh | Pyridines | |
dc.title | Antimicrobial activity of octenidine against multidrug-resistant Gram-negative pathogens. | |
dc.type | research article | |
dc.type.hasVersion | SMUR | |
dc.volume.number | 36 | |
dspace.entity.type | Publication |