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Establishment of an in vivo rat model for chronic musculoskeletal implant infection

BACKGROUND: 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 e...

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Autores principales: Witsø, Eivind, Hoang, Linh, Løseth, Kirsti, Bergh, Kåre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6975053/
https://www.ncbi.nlm.nih.gov/pubmed/31964416
http://dx.doi.org/10.1186/s13018-020-1546-6
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author Witsø, Eivind
Hoang, Linh
Løseth, Kirsti
Bergh, Kåre
author_facet Witsø, Eivind
Hoang, Linh
Løseth, Kirsti
Bergh, Kåre
author_sort Witsø, Eivind
collection PubMed
description BACKGROUND: 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.
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spelling pubmed-69750532020-01-28 Establishment of an in vivo rat model for chronic musculoskeletal implant infection Witsø, Eivind Hoang, Linh Løseth, Kirsti Bergh, Kåre J Orthop Surg Res Research Article BACKGROUND: 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. BioMed Central 2020-01-21 /pmc/articles/PMC6975053/ /pubmed/31964416 http://dx.doi.org/10.1186/s13018-020-1546-6 Text en © The Author(s). 2020 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Witsø, Eivind
Hoang, Linh
Løseth, Kirsti
Bergh, Kåre
Establishment of an in vivo rat model for chronic musculoskeletal implant infection
title Establishment of an in vivo rat model for chronic musculoskeletal implant infection
title_full Establishment of an in vivo rat model for chronic musculoskeletal implant infection
title_fullStr Establishment of an in vivo rat model for chronic musculoskeletal implant infection
title_full_unstemmed Establishment of an in vivo rat model for chronic musculoskeletal implant infection
title_short Establishment of an in vivo rat model for chronic musculoskeletal implant infection
title_sort establishment of an in vivo rat model for chronic musculoskeletal implant infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6975053/
https://www.ncbi.nlm.nih.gov/pubmed/31964416
http://dx.doi.org/10.1186/s13018-020-1546-6
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