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Updated: Feb 13, 2026

A Mouse Model to Assess Innate Immune Response to Staphylococcus aureus Infection
Published on: February 28, 2019
Staphylococcus aureus Membrane-Derived Vesicles Promote Bacterial Virulence and Confer Protective Immunity in Murine
Fatemeh Askarian1,2, John D Lapek3, Mitesh Dongre4
1Research Group of Host Microbe Interactions, Department of Medical Biology, Faculty of Health Sciences, UiT - The Arctic University of Norway, Tromsø, Norway.
Abstract:
Staphylococcus aureus produces membrane-derived vesicles (MVs), which share functional properties to outer membrane vesicles. Atomic force microscopy revealed that S. aureus-derived MVs are associated with the bacterial surface or released into the surrounding environment depending on bacterial growth conditions. By using a comparative proteomic approach, a total of 131 and 617 proteins were identified in MVs isolated from S. aureus grown in Luria-Bertani and brain-heart infusion broth, respectively. Purified S. aureus MVs derived from the bacteria grown in either media induced comparable levels of cytotoxicity and neutrophil-activation. Administration of exogenous MVs increased the resistance of S. aureus to killing by whole blood or purified human neutrophils ex vivo and increased S. aureus survival in vivo. Finally, immunization of mice with S. aureus-derived MVs induced production of IgM, total IgG, IgG1, IgG2a, and IgG2b resulting in protection against subcutaneous and systemic S. aureus infection. Collectively, our results suggest S. aureus MVs can influence bacterial-host interactions during systemic infections and provide protective immunity in murine models of infection.
Insights
Staphylococcus aureus membrane-derived vesicles (MVs) influence host interactions and survival. Immunizing mice with these MVs provides protection against S. aureus infections.
Area of Science:
- Microbiology
- Immunology
- Proteomics
Background:
- Staphylococcus aureus produces membrane-derived vesicles (MVs).
- These MVs share functional similarities with outer membrane vesicles.
- MV release is influenced by bacterial growth conditions.
Purpose of the Study:
- To characterize Staphylococcus aureus MVs.
- To investigate the role of MVs in bacterial pathogenesis and host immunity.
- To evaluate the potential of MVs as a vaccine candidate.
Main Methods:
- Atomic force microscopy to visualize MVs.
- Comparative proteomic analysis to identify MV proteins.
- In vitro assays for cytotoxicity and neutrophil activation.
- In vivo studies including bacterial survival and murine immunization models.
Main Results:
- Proteomic analysis identified significant differences in protein content of MVs based on growth media.
- S. aureus MVs induced comparable cytotoxicity and neutrophil activation.
- Exogenous MVs enhanced S. aureus resistance to host defenses and survival.
- Immunization with MVs conferred protection against S. aureus infection in mice.
Conclusions:
- Staphylococcus aureus MVs play a role in bacterial-host interactions during infection.
- S. aureus MVs can modulate the host immune response.
- S. aureus MVs hold promise as a protective vaccine strategy against S. aureus infections.
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