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dc.contributor.authorWitsø, Eivind
dc.contributor.authorHoang, Linh
dc.contributor.authorLøseth, Kirsti
dc.contributor.authorBergh, Kåre
dc.date.accessioned2022-05-04T09:22:39Z
dc.date.available2022-05-04T09:22:39Z
dc.date.created2020-10-29T15:20:19Z
dc.date.issued2020
dc.identifier.citationJournal of Orthopaedic Surgery and Research. 2020, 15 (1), 1-8.en_US
dc.identifier.issn1749-799X
dc.identifier.urihttps://hdl.handle.net/11250/2994086
dc.description.abstractBackground The aim of the study was to establish an experimental chronic musculoskeletal infection model in vivo characterized by (a) a small bacterial inoculum, (b) no general or local signs of infection, (c) several parallels (implants) in each animal and finally (d) a model that is technically easy to perform. Methods Bone xenografts with steel plates were implanted intramuscularly in rats. To the xenografts, different inocula of Staphylococcus aureus and two strains of Staphylococcus epidermidis were added. The animals were observed for different time periods before the removal of the xenografts. The xenografts and steel plates were subjected to quantitative bacterial culture after sonication. Additional steel plates were subjected to scanning electron microscopy (SEM) for visualization of biofilm formation. Results Inoculation of bone grafts with S. aureus did produce a pyogenic infection in all animals. A chronic infection was established in rats where the bone grafts were inoculated with S. epidermidis. A bacterial inoculum of 100 colony-forming units (CFU) of S. epidermidis was adequate as a minimum infective dose. During a period of up until 42 days, the animals infected with S. epidermidis had no general or local signs of infection. According to the results of the quantitative bacterial culture of sonicate fluid and SEM, a biofilm was developed on all implants. Conclusion In the present in vivo model, a very small bacterial inoculum succeeded in establishing a chronic musculoskeletal implant infection where a biofilm was formed on the implants. The experimental model is easy to perform and allows several implants in each animal. The model could be useful for the study of biofilm formation in vivo on different implants and different surfaces.en_US
dc.language.isoengen_US
dc.publisherBMCen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleEstablishment of an in vivo rat model for chronic musculoskeletal implant infectionen_US
dc.title.alternativeEstablishment of an in vivo rat model for chronic musculoskeletal implant infectionen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.pagenumber1-8en_US
dc.source.volume15en_US
dc.source.journalJournal of Orthopaedic Surgery and Researchen_US
dc.source.issue1en_US
dc.identifier.doi10.1186/s13018-020-1546-6
dc.identifier.cristin1843327
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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