Cargando…
Modeling Staphylococcus epidermidis-Induced Non-Unions: Subclinical and Clinical Evidence in Rats
S. epidermidis is one of the leading causes of orthopaedic infections associated with biofilm formation on implant devices. Open fractures are at risk of S. epidermidis transcutaneous contamination leading to higher non-union development compared to closed fractures. Although the role of infection i...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4721651/ https://www.ncbi.nlm.nih.gov/pubmed/26796958 http://dx.doi.org/10.1371/journal.pone.0147447 |
_version_ | 1782411252206665728 |
---|---|
author | Lovati, Arianna Barbara Romanò, Carlo Luca Bottagisio, Marta Monti, Lorenzo De Vecchi, Elena Previdi, Sara Accetta, Riccardo Drago, Lorenzo |
author_facet | Lovati, Arianna Barbara Romanò, Carlo Luca Bottagisio, Marta Monti, Lorenzo De Vecchi, Elena Previdi, Sara Accetta, Riccardo Drago, Lorenzo |
author_sort | Lovati, Arianna Barbara |
collection | PubMed |
description | S. epidermidis is one of the leading causes of orthopaedic infections associated with biofilm formation on implant devices. Open fractures are at risk of S. epidermidis transcutaneous contamination leading to higher non-union development compared to closed fractures. Although the role of infection in delaying fracture healing is well recognized, no in vivo models investigated the impact of subclinical low-grade infections on bone repair and non-union. We hypothesized that the non-union rate is directly related to the load of this commonly retrieved pathogen and that a low-grade contamination delays the fracture healing without clinically detectable infection. Rat femurs were osteotomized and stabilized with plates. Fractures were infected with a characterized clinical-derived methicillin-resistant S. epidermidis (10(3), 10(5), 10(8) colony forming units) and compared to uninfected controls. After 56 days, bone healing and osteomyelitis were clinically assessed and further evaluated by micro-CT, microbiological and histological analyses. The biofilm formation was visualized by scanning electron microscopy. The control group showed no signs of infection and a complete bone healing. The 10(3) group displayed variable response to infection with a 67% of altered bone healing and positive bacterial cultures, despite no clinical signs of infection present. The 10(5) and 10(8) groups showed severe signs of osteomyelitis and a non-union rate of 83–100%, respectively. The cortical bone reaction related to the periosteal elevation in the control group and the metal scattering detected by micro-CT represented limitations of this study. Our model showed that an intra-operative low-grade S. epidermidis contamination might prevent the bone healing, even in the absence of infectious signs. Our findings also pointed out a dose-dependent effect between the S. epidermidis inoculum and non-union rate. This pilot study identifies a relevant preclinical model to assess the role of subclinical infections in orthopaedic and trauma surgery and to test specifically designed diagnostic, prevention and therapeutic strategies. |
format | Online Article Text |
id | pubmed-4721651 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-47216512016-01-30 Modeling Staphylococcus epidermidis-Induced Non-Unions: Subclinical and Clinical Evidence in Rats Lovati, Arianna Barbara Romanò, Carlo Luca Bottagisio, Marta Monti, Lorenzo De Vecchi, Elena Previdi, Sara Accetta, Riccardo Drago, Lorenzo PLoS One Research Article S. epidermidis is one of the leading causes of orthopaedic infections associated with biofilm formation on implant devices. Open fractures are at risk of S. epidermidis transcutaneous contamination leading to higher non-union development compared to closed fractures. Although the role of infection in delaying fracture healing is well recognized, no in vivo models investigated the impact of subclinical low-grade infections on bone repair and non-union. We hypothesized that the non-union rate is directly related to the load of this commonly retrieved pathogen and that a low-grade contamination delays the fracture healing without clinically detectable infection. Rat femurs were osteotomized and stabilized with plates. Fractures were infected with a characterized clinical-derived methicillin-resistant S. epidermidis (10(3), 10(5), 10(8) colony forming units) and compared to uninfected controls. After 56 days, bone healing and osteomyelitis were clinically assessed and further evaluated by micro-CT, microbiological and histological analyses. The biofilm formation was visualized by scanning electron microscopy. The control group showed no signs of infection and a complete bone healing. The 10(3) group displayed variable response to infection with a 67% of altered bone healing and positive bacterial cultures, despite no clinical signs of infection present. The 10(5) and 10(8) groups showed severe signs of osteomyelitis and a non-union rate of 83–100%, respectively. The cortical bone reaction related to the periosteal elevation in the control group and the metal scattering detected by micro-CT represented limitations of this study. Our model showed that an intra-operative low-grade S. epidermidis contamination might prevent the bone healing, even in the absence of infectious signs. Our findings also pointed out a dose-dependent effect between the S. epidermidis inoculum and non-union rate. This pilot study identifies a relevant preclinical model to assess the role of subclinical infections in orthopaedic and trauma surgery and to test specifically designed diagnostic, prevention and therapeutic strategies. Public Library of Science 2016-01-21 /pmc/articles/PMC4721651/ /pubmed/26796958 http://dx.doi.org/10.1371/journal.pone.0147447 Text en © 2016 Lovati et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Lovati, Arianna Barbara Romanò, Carlo Luca Bottagisio, Marta Monti, Lorenzo De Vecchi, Elena Previdi, Sara Accetta, Riccardo Drago, Lorenzo Modeling Staphylococcus epidermidis-Induced Non-Unions: Subclinical and Clinical Evidence in Rats |
title | Modeling Staphylococcus epidermidis-Induced Non-Unions: Subclinical and Clinical Evidence in Rats |
title_full | Modeling Staphylococcus epidermidis-Induced Non-Unions: Subclinical and Clinical Evidence in Rats |
title_fullStr | Modeling Staphylococcus epidermidis-Induced Non-Unions: Subclinical and Clinical Evidence in Rats |
title_full_unstemmed | Modeling Staphylococcus epidermidis-Induced Non-Unions: Subclinical and Clinical Evidence in Rats |
title_short | Modeling Staphylococcus epidermidis-Induced Non-Unions: Subclinical and Clinical Evidence in Rats |
title_sort | modeling staphylococcus epidermidis-induced non-unions: subclinical and clinical evidence in rats |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4721651/ https://www.ncbi.nlm.nih.gov/pubmed/26796958 http://dx.doi.org/10.1371/journal.pone.0147447 |
work_keys_str_mv | AT lovatiariannabarbara modelingstaphylococcusepidermidisinducednonunionssubclinicalandclinicalevidenceinrats AT romanocarloluca modelingstaphylococcusepidermidisinducednonunionssubclinicalandclinicalevidenceinrats AT bottagisiomarta modelingstaphylococcusepidermidisinducednonunionssubclinicalandclinicalevidenceinrats AT montilorenzo modelingstaphylococcusepidermidisinducednonunionssubclinicalandclinicalevidenceinrats AT devecchielena modelingstaphylococcusepidermidisinducednonunionssubclinicalandclinicalevidenceinrats AT previdisara modelingstaphylococcusepidermidisinducednonunionssubclinicalandclinicalevidenceinrats AT accettariccardo modelingstaphylococcusepidermidisinducednonunionssubclinicalandclinicalevidenceinrats AT dragolorenzo modelingstaphylococcusepidermidisinducednonunionssubclinicalandclinicalevidenceinrats |