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Murine models of orthopedic infection featuring Staphylococcus aureus biofilm

Introduction: Osteomyelitis remains a major clinical challenge. Many published rodent fracture infection models are costly compared with murine models for rapid screening and proof-of-concept studies. We aimed to develop a dependable and cost-effective murine bone infection model that mimics bacteri...

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Autores principales: Dao, Aiken, O'Donohue, Alexandra K., Vasiljevski, Emily R., Bobyn, Justin D., Little, David G., Schindeler, Aaron
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Copernicus GmbH 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10134754/
https://www.ncbi.nlm.nih.gov/pubmed/37123502
http://dx.doi.org/10.5194/jbji-8-81-2023
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author Dao, Aiken
O'Donohue, Alexandra K.
Vasiljevski, Emily R.
Bobyn, Justin D.
Little, David G.
Schindeler, Aaron
author_facet Dao, Aiken
O'Donohue, Alexandra K.
Vasiljevski, Emily R.
Bobyn, Justin D.
Little, David G.
Schindeler, Aaron
author_sort Dao, Aiken
collection PubMed
description Introduction: Osteomyelitis remains a major clinical challenge. Many published rodent fracture infection models are costly compared with murine models for rapid screening and proof-of-concept studies. We aimed to develop a dependable and cost-effective murine bone infection model that mimics bacterial bone infections associated with biofilm and metal implants. Methods: Tibial drilled hole (TDH) and needle insertion surgery (NIS) infection models were compared in C57BL/6 mice (female, [Formula: see text] ). Metal pins were inserted selectively into the medullary canal adjacent to the defect sites on the metaphysis. Free Staphylococcus aureus (ATCC 12600) or biofilm suspension (ATCC 25923) was locally inoculated. Animals were monitored for physiological or radiographic evidence of infection without prophylactic antibiotics for up to 14 d. At the end point, bone swabs, soft-tissue biopsies, and metal pins were taken for cultures. X-ray and micro-CT scans were performed along with histology analysis. Results: TDH and NIS both achieved a 100 % infection rate in tibiae when a metal implant was present with injection of free bacteria. In the absence of an implant, inoculation with a bacterial biofilm still induced a 40 %–50 % infection rate. In contrast, freely suspended bacteria and no implant consistently showed lower or negligible infection rates. Micro-CT analysis confirmed that biofilm infection caused local bone loss even without a metal implant as a nidus. Although a metal surface permissive for biofilm formation is impermeable to create progressive bone infections in animal models, the metal implant can be dismissed if a bacterial biofilm is used. Conclusion: These models have a high potential utility for modeling surgery-related osteomyelitis, with NIS being simpler to perform than TDH.
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spelling pubmed-101347542023-04-28 Murine models of orthopedic infection featuring Staphylococcus aureus biofilm Dao, Aiken O'Donohue, Alexandra K. Vasiljevski, Emily R. Bobyn, Justin D. Little, David G. Schindeler, Aaron J Bone Jt Infect Original Full-Length Article Introduction: Osteomyelitis remains a major clinical challenge. Many published rodent fracture infection models are costly compared with murine models for rapid screening and proof-of-concept studies. We aimed to develop a dependable and cost-effective murine bone infection model that mimics bacterial bone infections associated with biofilm and metal implants. Methods: Tibial drilled hole (TDH) and needle insertion surgery (NIS) infection models were compared in C57BL/6 mice (female, [Formula: see text] ). Metal pins were inserted selectively into the medullary canal adjacent to the defect sites on the metaphysis. Free Staphylococcus aureus (ATCC 12600) or biofilm suspension (ATCC 25923) was locally inoculated. Animals were monitored for physiological or radiographic evidence of infection without prophylactic antibiotics for up to 14 d. At the end point, bone swabs, soft-tissue biopsies, and metal pins were taken for cultures. X-ray and micro-CT scans were performed along with histology analysis. Results: TDH and NIS both achieved a 100 % infection rate in tibiae when a metal implant was present with injection of free bacteria. In the absence of an implant, inoculation with a bacterial biofilm still induced a 40 %–50 % infection rate. In contrast, freely suspended bacteria and no implant consistently showed lower or negligible infection rates. Micro-CT analysis confirmed that biofilm infection caused local bone loss even without a metal implant as a nidus. Although a metal surface permissive for biofilm formation is impermeable to create progressive bone infections in animal models, the metal implant can be dismissed if a bacterial biofilm is used. Conclusion: These models have a high potential utility for modeling surgery-related osteomyelitis, with NIS being simpler to perform than TDH. Copernicus GmbH 2023-03-07 /pmc/articles/PMC10134754/ /pubmed/37123502 http://dx.doi.org/10.5194/jbji-8-81-2023 Text en Copyright: © 2023 Aiken Dao et al. https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this licence, visit https://creativecommons.org/licenses/by/4.0/
spellingShingle Original Full-Length Article
Dao, Aiken
O'Donohue, Alexandra K.
Vasiljevski, Emily R.
Bobyn, Justin D.
Little, David G.
Schindeler, Aaron
Murine models of orthopedic infection featuring Staphylococcus aureus biofilm
title Murine models of orthopedic infection featuring Staphylococcus aureus biofilm
title_full Murine models of orthopedic infection featuring Staphylococcus aureus biofilm
title_fullStr Murine models of orthopedic infection featuring Staphylococcus aureus biofilm
title_full_unstemmed Murine models of orthopedic infection featuring Staphylococcus aureus biofilm
title_short Murine models of orthopedic infection featuring Staphylococcus aureus biofilm
title_sort murine models of orthopedic infection featuring staphylococcus aureus biofilm
topic Original Full-Length Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10134754/
https://www.ncbi.nlm.nih.gov/pubmed/37123502
http://dx.doi.org/10.5194/jbji-8-81-2023
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