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dc.contributor.authorAskarian, Fatemeh
dc.contributor.authorLapek Jr., John D.
dc.contributor.authorDongre, Mitesh
dc.contributor.authorTsai, Chih-Ming
dc.contributor.authorKumaraswamy, Monika
dc.contributor.authorKousha, Armin
dc.contributor.authorValderrama, J. Andrés
dc.contributor.authorLudviksen, Judith K
dc.contributor.authorCavanagh, Jorunn Pauline
dc.contributor.authorUchiyama, Satoshi
dc.contributor.authorMollnes, Tom Eirik
dc.contributor.authorGonzalez, David J.
dc.contributor.authorWai, Sun Nyunt
dc.contributor.authorVictor, Nizet
dc.contributor.authorJohannessen, Mona
dc.date.accessioned2018-10-24T11:02:31Z
dc.date.available2018-10-24T11:02:31Z
dc.date.issued2018-02-20
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.sponsorshipNorthern Norway Regional Health Authority U.S. National Institutes of Health The Swedish Research Council UiT-The Arctic University of Norwayen_US
dc.descriptionThe 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.citationAskarian, 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.2018.00262en_US
dc.identifier.cristinIDFRIDAID 1561704
dc.identifier.doi10.3389/fmicb.2018.00262
dc.identifier.issn1664-302X
dc.identifier.urihttps://hdl.handle.net/10037/14028
dc.language.isoengen_US
dc.publisherFrontiers Mediaen_US
dc.relation.journalFrontiers in Microbiology
dc.rights.accessRightsopenAccessen_US
dc.subjectVDP::Medical disciplines: 700::Basic medical, dental and veterinary science disciplines: 710::Medical immunology: 716en_US
dc.subjectVDP::Medisinske Fag: 700::Basale medisinske, odontologiske og veterinærmedisinske fag: 710::Medisinsk immunologi: 716en_US
dc.titleStaphylococcus aureus Membrane-derived Vesicles Promote Bacterial Virulence and Confer Protective Immunity in Murine Infection Modelsen_US
dc.typeJournal articleen_US
dc.typeTidsskriftartikkelen_US
dc.typePeer revieweden_US


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