학술논문

Phenol-Soluble Modulins From Staphylococcus aureus Biofilms Form Complexes With DNA to Drive Autoimmunity
Document Type
article
Source
Subject
Biological Sciences
Biomedical and Clinical Sciences
Microbiology
Clinical Sciences
Medical Microbiology
Autoimmune Disease
Emerging Infectious Diseases
Infectious Diseases
2.1 Biological and endogenous factors
2.2 Factors relating to the physical environment
Aetiology
Infection
Amyloid
Animals
Autoimmune Diseases
Autoimmunity
Bacterial Toxins
Biofilms
DNA
Bacterial
Escherichia coli
Mice
Staphylococcal Infections
Staphylococcus aureus
PSM
Phenol Soluble Modulins
Staphycoccus aureus
biofilm
mesh
autoimmune disease
SLE
curli
Biochemistry and Cell Biology
Medical microbiology
Language
Abstract
The bacterial amyloid curli, produced by Enterobacteriales including Salmonella species and Escherichia coli, is implicated in the pathogenesis of several complex autoimmune diseases. Curli binds to extracellular DNA, and these complexes drive autoimmunity via production of anti-double-stranded DNA autoantibodies. Here, we investigated immune activation by phenol-soluble modulins (PSMs), the amyloid proteins expressed by Staphylococcus species. We confirmed the amyloid nature of PSMs expressed by S. aureus using a novel specific amyloid stain, (E,E)-1-fluoro-2,5-bis(3-hydroxycarbonyl-4-hydroxy) styrylbenzene (FSB). Direct interaction of one of the S. aureus PSMs, PSMα3, with oligonucleotides promotes fibrillization of PSM amyloids and complex formation with bacterial DNA. Finally, utilizing a mouse model with an implanted mesh-associated S. aureus biofilm, we demonstrated that exposure to S. aureus biofilms for six weeks caused anti-double-stranded DNA autoantibody production in a PSM-dependent manner. Taken together, these results highlight how the presence of PSM-DNA complexes in S. aureus biofilms can induce autoimmune responses, and suggest an explanation for how bacterial infections trigger autoimmunity.