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Evaluation of antibody responses to outer membrane vesicles (OMVs) and killed whole cell of Vibrio cholerae O1 El Tor in immunized mice

Authors :
Manijeh Sedaghat
Seyed Davar Siadat
Esmat Mirabzadeh
Malihe Keramati
Farzam Vaziri
Morvarid Shafiei
Fereshteh Shahcheraghi
Source :
Iranian Journal of Microbiology, Vol 11, Iss 3 (2019)
Publication Year :
2019
Publisher :
Tehran University of Medical Sciences, 2019.

Abstract

Background and Objectives: Cholera disease remains an important global health problem affecting 3-5 million subjects worldwide. Outer membrane vesicles (OMVs) have been found in a variety of Gram-negative bacteria and act as protective transport vesicles. The aim of this study was to evaluate Immune responses against Vibrio cholerae O1 El Tor clinical strain OMV and compare it with killed whole cell (KWC), complex of (KWC-OMV) as well as the internationally licensed oral cholera vaccine, Dukoral, in serum and intestinal secretions of mice. Materials and Methods: OMVs were prepared by using modified detergent-centrifugation procedure from V. cholerae O1 El Tor clinical strain from 2005 outbreak. The ultrastructure and content of OMVs were investigated via the Scanning Electron Microscopy (SEM) and SDS-PAGE analysis. Three doses of oral immunization were adjusted and total IgG and IgA in serum and intestinal secretion were measured by enzyme-linked immunosorbent assay (ELISA). Results: Extracted OMVs from the V. cholerae were spherical vesicles with a size ranging from 10 to 300 nm. OMV-immunized mice showed an increased level of total IgG and IgA both in serum and intestinal secretion when compared to the negative controls. Also, there existed a higher level of secretory IgA than the total IgG, suggesting the most of protection against V. cholerae colonization provided by sIgA. Conclusion: Our findings revealed that oral immunization with V. cholerae OMVs might induce a long-term immunity, especially when administered in combination with KWC. This study tested the adjuvant activity of OMVs and may be useful in future nano vaccine research.

Details

Language :
English
ISSN :
20083289 and 20084447
Volume :
11
Issue :
3
Database :
Directory of Open Access Journals
Journal :
Iranian Journal of Microbiology
Publication Type :
Academic Journal
Accession number :
edsdoj.478add191b2548869bd67de4ae51ae95
Document Type :
article
Full Text :
https://doi.org/10.18502/ijm.v11i3.1317