Rahim Muhammad Imran, Winkel Andreas, Lienenklaus Stefan, Stumpp Nico S, Szafrański Szymon P, Kommerein Nadine, Willbold Elmar, Reifenrath Janin, Mueller Peter P, Eisenburger Michael, Stiesch Meike
Department of Prosthetic Dentistry and Biomedical Materials Science, Hannover Medical School, Carl-Neuberg-Strasse 1, 30625 Hannover, Germany.
Lower Saxony Centre for Biomedical Engineering, Implant Research and Development (NIFE), Stadtfelddamm 34, 30625 Hannover, Germany.
Microorganisms. 2020 Oct 21;8(10):1624. doi: 10.3390/microorganisms8101624.
The performance of biomaterials is often compromised by bacterial infections and subsequent inflammation. So far, the conventional analysis of inflammatory processes in vivo involves time-consuming histology and biochemical assays. The present study employed a mouse model where interferon beta (IFN-β) is monitored as a marker for non-invasive rapid detection of inflammation in implant-related infections. The mouse model comprises subcutaneous implantation of morphologically modified titanium, followed by experimental infections with four taxonomically diverse oral bacteria: and (as mono culture or selected mixed-culture). IFN-β expression increased upon infections depending on the type of pathogen and was prolonged by the presence of the implant. IFN-β expression kinetics reduced with two mixed species infections when compared with the single species. Histological and confocal microscopy confirmed pathogen-specific infiltration of inflammatory cells at the implant-tissue interface. This was observed mainly in the vicinity of infected implants and was, in contrast to interferon expression, higher in infections with dual species. In summary, this non-invasive mouse model can be used to quantify longitudinally host inflammation in real time and suggests that the polymicrobial character of infection, highly relevant to clinical situations, has complex effects on host immunity.
生物材料的性能常常因细菌感染及随后的炎症反应而受损。到目前为止,体内炎症过程的传统分析涉及耗时的组织学和生化检测。本研究采用了一种小鼠模型,其中监测干扰素β(IFN-β)作为植入相关感染中炎症非侵入性快速检测的标志物。该小鼠模型包括皮下植入形态修饰的钛,随后用四种分类学上不同的口腔细菌进行实验性感染:以及(作为单一培养或选定的混合培养)。感染后,IFN-β表达根据病原体类型而增加,并因植入物的存在而延长。与单一物种感染相比,两种混合物种感染时IFN-β表达动力学降低。组织学和共聚焦显微镜检查证实了炎症细胞在植入物-组织界面的病原体特异性浸润。这主要在受感染植入物附近观察到,与干扰素表达相反,在双重物种感染中更高。总之,这种非侵入性小鼠模型可用于实时纵向定量宿主炎症,并表明与临床情况高度相关的感染的多微生物特征对宿主免疫有复杂影响。