Concurrent targeting of glycolysis in bacteria and host cell inflammation in septic arthritis

Concurrent targeting of glycolysis in bacteria and host cell inflammation in septic arthritis

Abstract 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 tha...

Full description

Saved in:
Bibliographic Details
Main Authors: Hyuk‐Kwon Kwon, Kristin E Yu, Sean V Cahill, Kareme D Alder, Christopher M Dussik, Sang‐Hun Kim, Lokesh Sharma, Jungho Back, Irvin Oh, Francis Y Lee
Format: Article
Language:English
Published: Springer Nature 2022-11-01
Series:EMBO Molecular Medicine
Subjects:
dimethyl fumarate
glycolysis
inflammation
MRSA
septic arthritis
Online Access:https://doi.org/10.15252/emmm.202115284
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Abstract 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.
ISSN:1757-4676
1757-4684

Similar Items