炎症
化脓性关节炎
关节炎
促炎细胞因子
免疫学
细胞内寄生虫
微生物学
医学
金黄色葡萄球菌
软骨
生物
细菌
免疫系统
遗传学
解剖
作者
Hyuk-Kwon Kwon,Kristin E. Yu,Sean V Cahill,Kareme D Alder,Christopher M. Dussik,Sang-Hun Kim,Lokesh Sharma,Jung Ho Back,Irvin Oh,Francis Y. Lee
标识
DOI:10.15252/emmm.202115284
摘要
Intracellular infiltration of bacteria into host cells complicates medical and surgical treatment of bacterial joint infections. Unlike soft tissue infections, septic arthritis and infection-associated inflammation destroy cartilage that does not regenerate once damaged. Herein, we show that glycolytic pathways are shared by methicillin-resistant Staphylococcus aureus (MRSA) proliferation and host inflammatory machinery in septic arthritis. MRSA readily penetrates host cells and induces proinflammatory cascades that persist after conventional antibiotic treatment. The glycolysis-targeting drug dimethyl fumarate (DMF) showed both bacteriostatic and anti-inflammatory effects by hindering the proliferation of intracellular MRSA and dampening excessive intraarticular inflammation. Combinatorial treatment with DMF and vancomycin further reduced the proliferation and re-emergence of intracellular MRSA. Combinatorial adjuvant administration of DMF with antibiotics alleviated clinical symptoms of septic arthritis by suppressing bacterial burden and curbing inflammation to protect cartilage and bone. Our results provide mechanistic insight into the regulation of glycolysis in the context of infection and host inflammation toward development of a novel therapeutic paradigm to ameliorate joint bioburden and destruction in septic arthritis.
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