dc.creatorBottero, Daniela
dc.creatorGaillard, María Emilia
dc.creatorErrea, Agustina Juliana
dc.creatorMoreno, Griselda Noemí
dc.creatorZurita, Maria Eugenia
dc.creatorPianciola, Luis
dc.creatorRumbo, Martín
dc.creatorHozbor, Daniela Flavia
dc.date.accessioned2017-09-12T13:58:35Z
dc.date.accessioned2018-11-06T14:44:02Z
dc.date.available2017-09-12T13:58:35Z
dc.date.available2018-11-06T14:44:02Z
dc.date.created2017-09-12T13:58:35Z
dc.date.issued2013-10
dc.identifierBottero, Daniela; Gaillard, María Emilia; Errea, Agustina Juliana; Moreno, Griselda Noemí; Zurita, Maria Eugenia; et al.; Outer membrane vesicles derived from Bordetella parapertussis as an acellular vaccine against Bordetella parapertussis and Bordetella pertussis infection; Elsevier; Vaccine; 31; 45; 10-2013; 5262-5268
dc.identifier0264-410X
dc.identifierhttp://hdl.handle.net/11336/23974
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1889619
dc.description.abstractBordetella parapertussis, a close related species of B. pertussis, can also cause the disease named pertussis or whooping cough. The number of cases caused by this related pathogen has risen sustained in the last years. The widely used cellular (wP) or acellular (aP) pertussis vaccines have little or no efficacy against B. parapertussis. In an effort to devise an effective acellular vaccine against B. parapertussis infection, outer membrane vesicles (OMVs) were obtained from B. parapertussis. Proteomic analysis of the resulting OMVs, designated OMVsBpp, evidenced the presence of several surface immunogens including pertactin. The characterized OMVsBpp were used in murine B. parapertussis intranasal challenge modelto examine their protective capacity when administered by systemic route. Immunized BALB/c mice were challenged with sublethal doses of B. parapertussis. Significant differences between immunized animals and the negative control group were observed (p < 0.001). OMVsBpp protected against B. parapertussis infection, whereas current commercial aP vaccine showed little protection against such pathogen. More interestingly, protection induced by OMVsBpp against B. pertussis was comparable to our previously designed vaccine consisting in OMVs derived from B. pertussis (OMVsBp). For these experiments we used as a positive control the current commercial aP vaccine in high dose. As expected aP offered protection against B. pertussis in mice. Altogether the results presented here showed that the OMVs from B. parapertussis are an attractive vaccine candidate to protect against whooping cough induced by B. parapertussis but also by B. pertussis.
dc.languageeng
dc.publisherElsevier
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.vaccine.2013.08.059
dc.relationinfo:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0264410X13011717
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectBordetella parapertussis
dc.subjectBordetella pertussis
dc.subjectAcellular vaccine
dc.subjectOMVs
dc.subjectProtection
dc.subjectWhooping cough
dc.titleOuter membrane vesicles derived from Bordetella parapertussis as an acellular vaccine against Bordetella parapertussis and Bordetella pertussis infection
dc.typeArtículos de revistas
dc.typeArtículos de revistas
dc.typeArtículos de revistas


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