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dc.rights.licenseopenen_US
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorPUGES, Mathilde
dc.contributor.authorBÉRARD, Xavier
hal.structure.identifierChimie et Biologie des Membranes et des Nanoobjets [CBMN]
dc.contributor.authorVILAIN, Sébastien
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorPEREYRE, Sabine
dc.contributor.authorSVAHN, Isabelle
dc.contributor.authorCARADU, Caroline
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorMZALI, Fatima
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorCAZANAVE, Charles
dc.date.accessioned2025-01-08T09:31:23Z
dc.date.available2025-01-08T09:31:23Z
dc.date.issued2023-10-01
dc.identifier.issn1532-2165en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/204190
dc.description.abstractEnThis study evaluated Staphylococcus aureus adhesion and biofilm formation on vascular grafts, which has seldom been investigated. Adhesion and biofilm formation capabilities of three methicillin susceptible S. aureus strains (one biofilm forming reference strain and two clinical isolates) on five different vascular biomaterials were evaluated in vitro, including polyester (P), P + gelatin (PG), P + collagen (PC), PC + silver (PCS), and PCS + triclosan (PCST). Staphylococcus aureus adhesion on grafts was evaluated after one hour of culture and biofilm formation after 24 hours of culture by four different methods: spectrophotometry after crystal violet staining; sonicate fluid culture; metabolic assay; and scanning electron microscopy (SEM). Optical density was compared using Mann-Whitney pairwise test, and bacterial counts using Wilcoxon pairwise test. PCST grafts were most efficient in preventing S. aureus adhesion and biofilm formation, regardless of the method used. Bacterial counts and metabolic activity were significantly lower on PCST grafts after 24 hours (5.65 vs. 9.24 [PCS], 8.99 [PC], 8.82 [PG], and 10.44 log CFU/mL [P]; p < .015), and only PCST grafts were bactericidal. Biofilm formation was significantly diminished on PCST grafts compared with all other grafts (p < .001). Bacterial viability and metabolic activity after 24 hours were more impaired on PG compared with PC graft, and were surprisingly higher on PCS compared with PC grafts. Biofilm biomass formed after exposure to P, PG, PC, and PCS grafts was also reduced after 24 hours of incubation with PCST grafts (p < .001). After 24 hours, few bacteria were visible by SEM on PCST grafts, whereas bacterial biofilm colonies were clearly identified on other graft surfaces. Triclosan impregnated PCST grafts appeared to interfere with S. aureus adhesion from early stages of biofilm formation in vitro. Silver impregnation was not efficient in preventing biofilm formation, and collagen coating promoted S. aureus biofilm formation more than gelatin coating.
dc.language.isoENen_US
dc.subject.enHumans
dc.subject.enStaphylococcus aureus
dc.subject.enTriclosan
dc.subject.enGelatin
dc.subject.enPolyesters
dc.subject.enSilver
dc.subject.enStaphylococcal Infections
dc.subject.enAnti-Bacterial Agents
dc.subject.enBiofilms
dc.subject.enCollagen
dc.title.enStaphylococcus aureus Adhesion and Biofilm Formation on Vascular Polyester Grafts are Inhibited In Vitro by Triclosan.
dc.title.alternativeEur J Vasc Endovasc Surgen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1016/j.ejvs.2023.07.018en_US
dc.subject.halSciences du Vivant [q-bio]/Médecine humaine et pathologieen_US
dc.identifier.pubmed37482281en_US
bordeaux.journalEuropean Journal of Vascular and Endovascular Surgeryen_US
bordeaux.page577-586en_US
bordeaux.volume66en_US
bordeaux.hal.laboratoriesMFP (Laboratoire Microbiologie Fondamentale et Pathogénicité) - UMR 5234en_US
bordeaux.issue4en_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.identifierhal-04872925
hal.version1
hal.date.transferred2025-01-08T09:31:25Z
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exporttrue
workflow.import.sourcepubmed
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&amp;rft_val_fmt=info:ofi/fmt:kev:mtx:journal&amp;rft.jtitle=European%20Journal%20of%20Vascular%20and%20Endovascular%20Surgery&amp;rft.date=2023-10-01&amp;rft.volume=66&amp;rft.issue=4&amp;rft.spage=577-586&amp;rft.epage=577-586&amp;rft.eissn=1532-2165&amp;rft.issn=1532-2165&amp;rft.au=PUGES,%20Mathilde&amp;B%C3%89RARD,%20Xavier&amp;VILAIN,%20S%C3%A9bastien&amp;PEREYRE,%20Sabine&amp;SVAHN,%20Isabelle&amp;rft.genre=article


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