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A Novel Mouse Model of Staphylococcus aureus Chronic Osteomyelitis That Closely Mimics the Human InfectionAn Integrated View of Disease Pathogenesis

机译:一种金黄色葡萄球菌慢性骨髓炎的新型小鼠模型,其紧密模拟人类感染疾病发病机理的综合观点

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Osteomyelitis is a serious bone infection typically caused by Staphylococcus aureus. The pathogenesis of osteomyelitis remains poorly understood, mainly for lack of experimental models that closely mimic human disease. We describe a novel murine model of metastatic chronic osteomyelitis initiated after intravenous inoculation of S. aureus microorganisms. The bacteria entered bones through the bloodstream and, after an acute phase with progressive growth (first 2 weeks after infection), they remained at constant numbers for up to 56 days (chronic phase). Clinical signs of illness and systemic inflammation were apparent only during the acute phase. Bone destruction and remodeling processes were readily detectable by magnetic resonance and X-ray imaging 3 weeks after infection, and high levels of bone deformation were observed during the chronic phase. Histological examination of infected bones demonstrated suppurative inflammation with foci of intense bacterial multiplication and necrosis during acute infection and osteoclastic resorption accompanied by new woven bone formation during chronic infection. Transmission electron microscopy revealed S. aureus microorganisms forming microcolonies within the nonmineralized collagen matrix or located intracellularly within neutrophils. In summary, our mouse model of staphylococcal hematogenous osteomyelitis precisely reproduces most features of the human disease. Although the extent of lesions in the chronic phase was subject to variation, this model is ideal for testing and monitoring novel treatment modalities via noninvasive imaging.
机译:骨髓炎是一种严重的骨感染,通常由金黄色葡萄球菌引起。骨髓炎的发病机理仍然知之甚少,主要是因为缺乏紧密模拟人类疾病的实验模型。我们描述了金黄色葡萄球菌微生物的静脉接种后启动的转移性慢性骨髓炎的新型鼠模型。细菌通过血液进入骨骼,并在逐渐发展的急性期(感染后的前两周)后保持恒定的数量达56天(慢性期)。仅在急性期才出现疾病和全身性炎症的临床体征。感染后3周,通过磁共振和X射线成像很容易检测到骨破坏和重塑过程,并且在慢性期观察到高水平的骨变形。受感染的骨头的组织学检查表明,化脓性炎症是急性感染期间细菌大量繁殖和坏死的病灶,而在慢性感染期间破骨细胞吸收伴随新的编织骨形成。透射电子显微镜显示金黄色葡萄球菌微生物在非矿化胶原基质内或在嗜中性粒细胞内位于细胞内形成小菌落。总而言之,我们的葡萄球菌性血源性骨髓炎小鼠模型精确地再现了人类疾病的大多数特征。尽管慢性阶段的病变程度会发生变化,但该模型非常适合通过无创成像测试和监测新型治疗方式。

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