Division of Orthopaedics and Traumatology, Department of Orthopaedics, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Guangdong Provincial Key Laboratory of Bone and Cartilage Regenerative Medicine, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Infect Immun. 2021 Apr 16;89(5). doi: 10.1128/IAI.00814-20.
To investigate the molecular pathogenesis of bone with osteomyelitis, we developed implant-associated osteomyelitis (IAOM) models in mice. An orthopedic stainless pin was surgically placed in the right femoral midshaft of mice, followed by an inoculation of into the medullary cavity. Typical characteristics of IAOM, like periosteal reaction and intraosseous abscess, occurred by day 14 postinfection. By day 28 postinfection, necrotic abscess, sequestrum formation, and deformity of the whole femur were observed. Transcriptional analysis identified 101 and 1,702 differentially expressed genes (DEGs) between groups by days 3 and 14 postinfection, respectively. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes analyses revealed the enrichment of pathways in response to the bacterium, receptor-ligand activity, and chemokine signaling by day 3 postinfection. However, by day 14 postinfection, the enrichment switched to angiogenesis, positive regulation of cell motility and migration, skeletal system development, and cytokine-cytokine receptor interaction. Furthermore, protein-protein interaction network analysis identified 4 cytokines (interleukin 6 [IL-6], Cxcl10, gamma interferon [IFN-γ], and Cxcl9) associated with IAOM at an early stage of infection. Overall, as the pathological changes in this mouse model were consistent with those in human IAOM, our model may be used to investigate the mechanism and treatment of IAOM. Furthermore, the data for transcriptome sequencing and bioinformatic analysis will be an important resource for dissecting the molecular pathogenesis of bone with IAOM.
为了研究骨髓炎的分子发病机制,我们在小鼠中建立了与植入物相关的骨髓炎(IAOM)模型。将骨科不锈钢钉通过手术植入小鼠右侧股骨中段,然后将接种物注入骨髓腔。感染后第 14 天,出现典型的 IAOM 特征,如骨膜反应和骨内脓肿。感染后第 28 天,观察到坏死性脓肿、死骨形成和整个股骨畸形。转录分析确定感染后第 3 天和第 14 天两组之间分别有 101 和 1702 个差异表达基因(DEGs)。基因本体论和京都基因与基因组百科全书分析显示,感染后第 3 天,对细菌的反应、受体配体活性和趋化因子信号通路的富集。然而,感染后第 14 天,富集切换到血管生成、细胞运动和迁移的正调节、骨骼系统发育和细胞因子-细胞因子受体相互作用。此外,蛋白质-蛋白质相互作用网络分析确定了 4 种细胞因子(白细胞介素 6 [IL-6]、Cxcl10、γ干扰素[IFN-γ]和 Cxcl9)在感染早期与 IAOM 相关。总的来说,由于该小鼠模型的病理变化与人的 IAOM 一致,我们的模型可能用于研究 IAOM 的发病机制和治疗方法。此外,转录组测序和生物信息学分析的数据将是剖析 IAOM 中骨分子发病机制的重要资源。