Walton Kelly D, Lord Allison, Kendall Lon V, Dow Steven W
Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, Colorado, USA.
Department of Microbiology, Immunology and Pathology, Department of Clinical Sciences, Center for Immune and Regenerative Medicine, Colorado State University, Fort Collins, Colorado, USA.
Comp Med. 2014 Feb;64(1):25-33.
Biofilm formation represents a unique mechanism by which Staphylococcus aureus and other microorganisms avoid antimicrobial clearance and establish chronic infections. Treatment of these infections can be challenging, because the bacteria in the biofilm state are often resistant to therapies that are effective against planktonic bacteria of the same species. Effective animal models for the study of biofilm infections and novel therapeutics are needed. In addition, there is substantial interest in the use of noninvasive, in vivo data collection techniques to decrease the animal numbers required for the execution of infectious disease studies. To ad- dress these needs, we evaluated 3 murine models of implant-associated biofilm infection by using in vivo bioluminescent imaging techniques. The goal of these studies was to identify the model that was most amenable to development of sustained infections that could be imaged repeatedly in vivo by using bioluminescent technology. We found that the subcutaneous mesh and tibial intramedullary pin models both maintained consistent levels of bioluminescence for as long as 35 d after infection, with no implant loss experienced in either model. In contrast, a subcutaneous catheter model demonstrated significant incidence of incisional ab- scessation and implant loss by day 20 after infection. The correlation of bioluminescent measurements and bacterial enumeration was strongest with the subcutaneous mesh model. Among the 3 models we evaluated, the subcutaneous mesh model is the most appropriate animal model for prolonged study of biofilm infections by using bioluminescent imaging.
生物膜形成是金黄色葡萄球菌和其他微生物逃避抗菌清除并建立慢性感染的一种独特机制。这些感染的治疗可能具有挑战性,因为处于生物膜状态的细菌通常对针对同一物种浮游细菌有效的疗法具有抗性。需要有效的动物模型来研究生物膜感染和新型疗法。此外,人们对使用非侵入性体内数据收集技术以减少进行传染病研究所需的动物数量有着浓厚兴趣。为满足这些需求,我们通过使用体内生物发光成像技术评估了3种植入物相关生物膜感染的小鼠模型。这些研究的目的是确定最适合发展持续性感染的模型,该感染可通过生物发光技术在体内反复成像。我们发现,皮下网片和胫骨髓内针模型在感染后长达35天内均保持一致的生物发光水平,两种模型均未出现植入物丢失。相比之下,皮下导管模型在感染后第20天出现切口脓肿和植入物丢失的发生率较高。皮下网片模型的生物发光测量与细菌计数之间的相关性最强。在我们评估的3种模型中,皮下网片模型是使用生物发光成像对生物膜感染进行长期研究的最合适动物模型。