Cassandra L Brinkman, Suzannah M Schmidt-Malan, Melissa J Karau, Robin Patel
{"title":"A novel rat model of foreign body osteomyelitis for evaluation of antimicrobial efficacy.","authors":"Cassandra L Brinkman, Suzannah M Schmidt-Malan, Melissa J Karau, Robin Patel","doi":"10.20454/jeaas.2019.1555","DOIUrl":null,"url":null,"abstract":"<p><p>The most common organism-type causing orthopedic foreign body infection is the staphylococci, of which <i>Staphylococcus aureus</i> and <i>Staphylococcus epidermidis</i> are especially common. These organisms form biofilms on orthopedic foreign body surfaces, rendering such infections challenging and time consuming to treat. Our group evaluates novel therapeutics for orthopedic foreign body infection in animal models. A current limitation of most animal models is that that they only allow for the removal of one sample per animal, at the time of sacrifice. Herein, we describe a novel rat model of foreign body osteomyelitis that allows removal of foreign bodies at different time points, from the same infected animal. We demonstrate that this model can be used for both <i>S. aureus</i> and <i>S. epidermidis</i> orthopedic foreign body infection, with 3.56, 3.60 and 5.51 log<sub>10</sub> cfu/cm<sup>2</sup> <i>S. aureus</i> recovered at four, five and six weeks, respectively, after infection, and 2.08, 2.17 and 2.62 log<sub>10</sub> cfu/cm<sup>2</sup> <i>S. epidermidis</i> recovered at four, five and six weeks, respectively, after infection We evaluated the model with <i>S. aureus</i> infection treated with rifampin 25 mg/kg twice daily for 21 days. Using quantitative cultures, we were no longer able to detect bacteria as of the 14th day of treatment with bacteria becoming detectable again 7 days following die discontinuation of rifampin a period. This novel model allows monitoring of evolution of infection at the infection site in the same animal.</p>","PeriodicalId":92805,"journal":{"name":"Journal of experimental and applied animal sciences","volume":"3 1 1","pages":"7-14"},"PeriodicalIF":0.0000,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6688763/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of experimental and applied animal sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.20454/jeaas.2019.1555","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
The most common organism-type causing orthopedic foreign body infection is the staphylococci, of which Staphylococcus aureus and Staphylococcus epidermidis are especially common. These organisms form biofilms on orthopedic foreign body surfaces, rendering such infections challenging and time consuming to treat. Our group evaluates novel therapeutics for orthopedic foreign body infection in animal models. A current limitation of most animal models is that that they only allow for the removal of one sample per animal, at the time of sacrifice. Herein, we describe a novel rat model of foreign body osteomyelitis that allows removal of foreign bodies at different time points, from the same infected animal. We demonstrate that this model can be used for both S. aureus and S. epidermidis orthopedic foreign body infection, with 3.56, 3.60 and 5.51 log10 cfu/cm2S. aureus recovered at four, five and six weeks, respectively, after infection, and 2.08, 2.17 and 2.62 log10 cfu/cm2S. epidermidis recovered at four, five and six weeks, respectively, after infection We evaluated the model with S. aureus infection treated with rifampin 25 mg/kg twice daily for 21 days. Using quantitative cultures, we were no longer able to detect bacteria as of the 14th day of treatment with bacteria becoming detectable again 7 days following die discontinuation of rifampin a period. This novel model allows monitoring of evolution of infection at the infection site in the same animal.