IAI FigSearch
Home Help [Feedback] [For Subscribers] [Archive] [Search] --
IAI Accepts, published online ahead of print on 4 August 2008
This Article
Right arrow Full Text (PDF)
Right arrow Other Versions of this Article:
IAI.00532-08v1
76/10/4554    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Google Scholar
Right arrow Articles by Schild, S.
Right arrow Articles by Camilli, A.
PubMed
Right arrow PubMed Citation
Right arrow Articles by Schild, S.
Right arrow Articles by Camilli, A.

 Previous Article  |  Next Article 

Infect. Immun. doi:10.1128/IAI.00532-08
Copyright (c) 2008, American Society for Microbiology and/or the Listed Authors/Institutions. All Rights Reserved.

Immunization with Vibrio cholerae outer membrane vesicles induces protective immunity in mice

Stefan Schild, Eric J. Nelson, and Andrew Camilli*

Howard Hughes Medical Institute and the Department of Molecular Biology and Microbiology, Tufts University School of Medicine, Boston, MA 02111, U.S.A.; Institut fuer Molekulare Biowissenschaften, Karl-Franzens-Universitaet Graz, Humboldtstrasse 50, 8010 Graz, Austria

* To whom correspondence should be addressed. Email: andrew.camilli{at}tufts.edu.


   Abstract

The Gram-negative bacterium Vibrio cholerae releases outer membrane vesicles (OMVs) during growth. In this study we immunized female mice by the intranasal, intragastric or intraperitoneal routes with purified OMVs derived from V. cholerae. Independent of the route of immunization, mice induced a specific, high titer immune response of similar level against a variety of antigens present in the OMVs. After the last immunization, the half-maximum total immunoglobulin titer was stable over a three month period indicating that the immune response was long-lasting. The induction of specific isotypes was however dependent on the immunization route. IgA, for example, was only induced to a significant level by mucosal immunization, with the intranasal route generating the highest titers. We challenged the offspring of immunized female mice with V. cholerae via the oral route in two consecutive periods approximately 30 and 95 days after the last immunization. Regardless of the route of immunization, the offspring was protected against colonization with V. cholerae in both challenge periods. Our results show that both routes of mucosal immunization with OMVs derived from V. cholerae induce a long-term protective immune response against this gastrointestinal pathogen. These findings may contribute to the development of ‘non-living’, OMV-based vaccines against V. cholerae and other enteric pathogens, using a oral or intranasal routes of immunization.




This article has been cited by other articles:




Home Help [Feedback] [For Subscribers] [Archive] [Search] --
J. Bacteriol. J. Virol. Eukaryot. Cell
Microbiol. Mol. Biol. Rev. Clin. Vaccine Immunol. All ASM Journals

Copyright © 2008 by the American Society for Microbiology. All rights reserved.