4.7 Article

Lipoproteins Are Responsible for the Pro-Inflammatory Property of Staphylococcus aureus Extracellular Vesicles

Journal

Publisher

MDPI
DOI: 10.3390/ijms22137099

Keywords

Staphylococcus aureus; extracellular vesicles; lipoproteins; inflammation; TLR2

Funding

  1. Swedish Medical Research Council [523-2013-2750, 2019-01135]
  2. Swedish Government
  3. ALF-agreement [ALFGBG823941, ALFGBG-933787]
  4. Wilhelm and Martina Lundgren Foundation [2019-3163]
  5. Rune och Ulla Amlovs Stiftelse for Neurologisk och Reumatologisk Forskning
  6. Adlerbertska Forskningsstiftelsen
  7. E och K.G. Lennanders stipendiestiftels
  8. Deutsche Forschungsgemeinschaft [EXC 2124-390838134]
  9. Swedish Research Council [2019-01135] Funding Source: Swedish Research Council

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Staphylococcal aureus extracellular vesicles can induce inflammatory responses in host cells, with lipidated lipoproteins (Lpp) playing a crucial role in this activity while cell wall anchoring of surface proteins does not contribute to immune stimulation.
Staphylococcal aureus (S. aureus), a Gram-positive bacteria, is known to cause various infections. Extracellular vesicles (EVs) are a heterogeneous array of membranous structures secreted by cells from all three domains of life, i.e., eukaryotes, bacteria, and archaea. Bacterial EVs are implied to be involved in both bacteria-bacteria and bacteria-host interactions during infections. It is still unclear how S. aureus EVs interact with host cells and induce inflammatory responses. In this study, EVs were isolated from S. aureus and mutant strains deficient in either prelipoprotein lipidation (Delta lgt) or major surface proteins (Delta srtAB). Their immunostimulatory capacities were assessed both in vitro and in vivo. We found that S. aureus EVs induced pro-inflammatory responses both in vitro and in vivo. However, this activity was dependent on lipidated lipoproteins (Lpp), since EVs isolated from the Delta lgt showed no stimulation. On the other hand, EVs isolated from the Delta srtAB mutant showed full immune stimulation, indicating the cell wall anchoring of surface proteins did not play a role in immune stimulation. The immune stimulation of S. aureus EVs was mediated mainly by monocytes/macrophages and was TLR2 dependent. In this study, we demonstrated that not only free Lpp but also EV-imbedded Lpp had high pro-inflammatory activity.

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