dc.contributor.author | Askarian, Fatemeh | |
dc.contributor.author | Lapek Jr., John D. | |
dc.contributor.author | Dongre, Mitesh | |
dc.contributor.author | Tsai, Chih-Ming | |
dc.contributor.author | Kumaraswamy, Monika | |
dc.contributor.author | Kousha, Armin | |
dc.contributor.author | Valderrama, J. Andrés | |
dc.contributor.author | Ludviksen, Judith K | |
dc.contributor.author | Cavanagh, Jorunn Pauline | |
dc.contributor.author | Uchiyama, Satoshi | |
dc.contributor.author | Mollnes, Tom Eirik | |
dc.contributor.author | Gonzalez, David J. | |
dc.contributor.author | Wai, Sun Nyunt | |
dc.contributor.author | Victor, Nizet | |
dc.contributor.author | Johannessen, Mona | |
dc.date.accessioned | 2018-10-24T11:02:31Z | |
dc.date.available | 2018-10-24T11:02:31Z | |
dc.date.issued | 2018-02-20 | |
dc.description.abstract | <i>Staphylococcus aureus</i> produces membrane-derived vesicles (MVs), which share functional properties to outer membrane vesicles. Atomic force microscopy revealed that <i>S. aureus</i>-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 <i>S. aureus</i> grown in Luria-Bertani and brain-heart infusion broth, respectively. Purified <i>S. aureus</i> 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 <i>S. aureus</i> to killing by whole blood or purified human neutrophils ex vivo and increased <i>S. aureus</i> survival in vivo. Finally, immunization of mice with <i>S. aureus</i>-derived MVs induced production of IgM, total IgG, IgG1, IgG2a, and IgG2b resulting in protection against subcutaneous and systemic <i>S. aureus</i> infection. Collectively, our results suggest <i>S. aureus</i> MVs can influence bacterial–host interactions during systemic infections and provide protective immunity in murine models of infection. | en_US |
dc.description.sponsorship | Northern Norway Regional Health Authority
U.S. National Institutes of Health
The Swedish Research Council
UiT-The Arctic University of Norway | en_US |
dc.description | The following article, Askarian, F., Lapek, J.D.Jr., Dongre, M., Tsai, C.-M., Kumaraswamy, M., Kousha, A., ... Johannessen, M. (2018). Staphylococcus aureus Membrane-derived Vesicles Promote Bacterial Virulence and Confer Protective Immunity in Murine Infection Models. <i>Frontiers in Microbiology</i>, 9(262). https://doi.org/10.3389/fmicb.2018.00262, can be accessed at <a href=https://doi.org/10.3389/fmicb.2018.00262> https://doi.org/10.3389/fmicb.2018.00262</a>. | en_US |
dc.identifier.citation | Askarian, F., Lapek, J.D.Jr., Dongre, M., Tsai, C.-M., Kumaraswamy, M., Kousha, A., ... Johannessen, M. (2018). Staphylococcus aureus Membrane-derived Vesicles Promote Bacterial Virulence and Confer Protective Immunity in Murine Infection Models. Frontiers in Microbiology, 9(262). https://doi.org/10.3389/fmicb.2018.00262 | en_US |
dc.identifier.cristinID | FRIDAID 1561704 | |
dc.identifier.doi | 10.3389/fmicb.2018.00262 | |
dc.identifier.issn | 1664-302X | |
dc.identifier.uri | https://hdl.handle.net/10037/14028 | |
dc.language.iso | eng | en_US |
dc.publisher | Frontiers Media | en_US |
dc.relation.journal | Frontiers in Microbiology | |
dc.rights.accessRights | openAccess | en_US |
dc.subject | VDP::Medical disciplines: 700::Basic medical, dental and veterinary science disciplines: 710::Medical immunology: 716 | en_US |
dc.subject | VDP::Medisinske Fag: 700::Basale medisinske, odontologiske og veterinærmedisinske fag: 710::Medisinsk immunologi: 716 | en_US |
dc.title | Staphylococcus aureus Membrane-derived Vesicles Promote Bacterial Virulence and Confer Protective Immunity in Murine Infection Models | en_US |
dc.type | Journal article | en_US |
dc.type | Tidsskriftartikkel | en_US |
dc.type | Peer reviewed | en_US |