4.8 Article

Immunomodulatory effects exerted by extracellular vesicles from Staphylococcus epidermidis and Staphylococcus aureus isolated from bone-anchored prostheses

Journal

BIOMATERIALS
Volume 278, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2021.121158

Keywords

Chemokines; Cytokines; Cytotoxicity; Biomaterial-associated infection; Extracellular vesicles; Monocyte; Macrophage; Inflammation; Staphylococci; THP-1

Funding

  1. Swedish Research Council [2018-02891]
  2. Swedish government
  3. county councils [ALFGBG-725641]
  4. European Union [754412]
  5. CARe -Centre for Antibiotic Resistance Research at University of Gothenburg
  6. IngaBritt and Arne Lundberg Foundation
  7. Eivind and Elsa K: son Sylvan Foundation
  8. Hjalmar Svensson Foundation
  9. Adlerbertska Foundation
  10. Doctor Felix Neubergh Foundation
  11. GU Biomaterials within the Strategic Research Area initiative
  12. Svenska Sallskapet for Medicinsk Forskning (SSMF)
  13. Osteology Foundation, Switzerland
  14. Helfrid Johansson's Foundation
  15. Marie Curie Actions (MSCA) [754412] Funding Source: Marie Curie Actions (MSCA)
  16. Swedish Research Council [2018-02891] Funding Source: Swedish Research Council

Ask authors/readers for more resources

This study found that Staphylococcus aureus and Staphylococcus epidermidis isolated from osteomyelitis associated with septic loosening of orthopedic prostheses release extracellular vesicles (EVs) with potent cytolytic and immunomodulatory properties.
Staphylococcus aureus and Staphylococcus epidermidis are the bacteria that most frequently cause osteomyelitis. This study aimed to determine whether staphylococci isolated from osteomyelitis associated with septic loosening of orthopedic prostheses release extracellular vesicles (EVs) and, if so, to determine tentative immunomodulatory effects on the human monocytic cell line THP-1. EVs were isolated from bacterial cultures using filtration and ultracentrifugation and characterized by scanning electron microscopy, nanoparticle tracking analysis and Western Blot. The cytotoxic effect of EVs was analyzed by Nucleo Counter and lactate dehydrogenase (LDH) analyses. Confocal laser scanning microscopy was employed to visualize the uptake of EVs by THP-1 cells. Activation of the transcription factor nuclear factor-kappa B (NF-kappa B) was determined in THP1-Blue T NF-kappa B cells, and the gene expression and secretion of cytokines were determined by quantitative polymerase chain reaction and enzyme-linked immunosorbent assay, respectively. All investigated strains, irrespective of their biofilm formation ability, were able to secrete EVs in vitro. The S. aureus strains produced significantly more EVs than the S. epidermidis strains. Both S. aureus-derived EVs and S. epidermidis-derived EVs were internalized by THP-1 cells, upregulated Toll-like receptor 3 (TLR3) gene expression, activated NF-kappa B, and promoted the gene expression and secretion of interleukin (IL)-8, monocyte chemoattractant protein (MCP)-1, matrix metallopeptidase (MMP)-9 and IL-10. Whereas EVs from both staphylococcal species upregulated the proapoptotic DNA damage-inducible transcript 4 (DDIT4) gene and downregulated the antiapoptotic B-cell lymphoma 2 (Bcl-2) gene, cytolysis was preferentially induced in S. aureus EV-stimulated cells, possibly related to the expression of cytolytic proteins predominantly in S. aureus EVs. In conclusion, staphylococcal EVs possess potent cytolytic and immunomodulatory properties.

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