dc.creator | Bottero, Daniela | |
dc.creator | Zurita, María Eugenia | |
dc.creator | Gaillard, María Emilia | |
dc.creator | Carriquiriborde, Francisco Pablo | |
dc.creator | Aispuro, Pablo Martín | |
dc.creator | Elizagaray, Maia Lina | |
dc.creator | Bartel, Erika Belén | |
dc.creator | Castuma, Celina Elisabet | |
dc.creator | Hozbor, Daniela Flavia | |
dc.date | 2018 | |
dc.date | 2020-09-14T16:57:51Z | |
dc.date.accessioned | 2023-07-14T22:00:14Z | |
dc.date.available | 2023-07-14T22:00:14Z | |
dc.identifier | http://sedici.unlp.edu.ar/handle/10915/104549 | |
dc.identifier | http://hdl.handle.net/11336/96469 | |
dc.identifier | https://www.frontiersin.org/articles/10.3389/fimmu.2018.02501/full | |
dc.identifier | issn:1664-3224 | |
dc.identifier.uri | https://repositorioslatinoamericanos.uchile.cl/handle/2250/7445233 | |
dc.description | <i>Bordetella parapertussis</i> is a respiratory-disease pathogen producing symptomatology similar to that of pertussis but of underestimated incidence and with no specific vaccine existing. We recently designed a vaccine candidate from <i>B. parapertussis</i> outer-membrane vesicles (OMVs) that proved to be safe and protective in a murine-infection model. Based on protection recently reported for the <i>B. parapertussis</i> O antigen in aqueous solution, we assessed here whether the <i>B. parapertussis</i> O-antigen-containing lipopolysaccharide (BppLPS-O⁺) embedded in the membranes, as present in <i>B. parapertussis</i>-derived OMVs (OMVs(Bpp-LPS-O⁺)), was the component responsible for that previously observed protection by OMVs. By performing a comparative study with OMVs from a human strain with undetectable O antigen (OMVs(Bpp-LPS-O⁻)), we demonstrated that the OMVs(Bpp-LPS-O⁺), but not the OMVs(Bpp-LPS-O⁻), protected mice against sublethal <i>B. parapertussis</i> infections. Indeed, the <i>B. parapertussis</i> loads were significantly reduced in the lungs of OMVs(Bpp-LPS-O⁺) -vaccinated animals, with the CFUs recovered being decreased by 4 log units below those detected in the non-immunized animals or in the animals treated with the OMVs(Bpp-LPS-O⁻), (p < 0.001). We detected that the OMVs(Bpp-LPS-O⁺) induced IgG antibodies against <i>B. parapertussis</i> whole-cell lysates, which immunocomponents recognized, among others, the O antigen and accordingly conferred protection against <i>B. parapertussis</i> infection, as observed in <i>in-vivo</i>-passive-transfer experiments. Of interest was that the OMVs(Bpp-LPS-O⁺) -generated sera had opsonophagocytic and bactericidal capabilities that were not detected with the OMVs(Bpp-LPS-O⁻)-induced sera, suggesting that those activities were involved in the clearance of <i>B. parapertussis</i>. Though stimulation of cultured spleen cells from immunized mice with formulations containing the O antigen resulted in gamma interferon (IFN-γ) and interleukin-17 production, spleen cells from OMVs(Bpp-LPS-O⁺) -immunized mice did not significantly contribute to the observed protection against <i>B. parapertussis</i> infection. The protective capability of the <i>B. parapertussis</i> O antigen was also detected in formulations containing both the OMVs derived from B. pertussis and purified BppLPS-O⁺. This combined formulation protected mice against B. pertussis along with <i>B. parapertussis</i>. | |
dc.description | Facultad de Ciencias Exactas | |
dc.description | Instituto de Biotecnologia y Biologia Molecular | |
dc.description | Instituto de Estudios Inmunológicos y Fisiopatológicos | |
dc.format | application/pdf | |
dc.language | en | |
dc.rights | http://creativecommons.org/licenses/by/4.0/ | |
dc.rights | Creative Commons Attribution 4.0 International (CC BY 4.0) | |
dc.subject | Ciencias Exactas | |
dc.subject | Biología | |
dc.subject | Bordetella parapertussis | |
dc.subject | lipopolysacharides | |
dc.subject | O-antigen | |
dc.subject | outer-membrane vesicles | |
dc.subject | protection | |
dc.title | Outer-Membrane-Vesicle-Associated O Antigen, a Crucial Component for Protecting Against Bordetella parapertussis Infection | |
dc.type | Articulo | |
dc.type | Articulo | |