Jundishapur Journal of Microbiology
Ahvaz Jundishapur University of Medical Sciences
Authors
2,*, Mohammad Reza Aghasadeghi1, Mohamad Piryaie3, Shahin Najar Peerayeh4, Seyed Fazlollah Mousavi2, Arfa Moshiri5, Seyed Mehdi Sadat1, Mehrangiz Zangeneh6, Mehdi Nejati2, Nafiseh Kashanizadeh7, Saied Bouzari8,*Neisseria meningitidis Serogroup A, is a major cause of bacterial meningitidis outbreaks in Africa and the Middle East. While polysaccharide vaccines have been available for many years, these vaccines have many disadvantages including the induction of T-cell independent responses which do not induce memory responses.
Thus to overcome this problem, in this research outer membrane vesicle (OMV) containing PorA was extracted and evaluated by biological and immunological methods.
OMVs were extracted with deoxycholate and EDTA, and purification was performed by sequential ultracentrifugation. Physicochemical properties of extracted OMVs were analyzed by electron microscopy and SDS-PAGE. The toxicity of LPS content in its was assayed by LAL test. The Presence of PorA as a major component of OMV was confirmed by western blot. To study antibodies synthesis after immunization with OMV, ELISA method was used. Also serum bactericidal assay (SBA) was performed to determine the serum bactericidal activity against N. meningitidis serogroup A.
The results revealed that the content of protein extracted was 0.1 mg/mL. The electron microscopy showed that intactness of the vesicle in these preparation ranged more than 70%. The SDS-PAGE showed that PorA as a major immunological part of outer membrane vesicle was located in 35-40kDa. LAL test showed that the endotoxin activity was around 126EU/mL which is safe for using. The ELISA test revealed that the IgG total titer was elevated after the first injection. SBA indicates that bactericidal antibodies rise after the second dose of booster.
The results showed that the extracted OMVs were conformationally stable, and there were no pyrogenic determinants in OMV. Also the results showed that the OMV elicited high level of specific antibodies against N. meningitidis serogroup A. These results indicate that the OMV obtained here, can be used as a meningococcal vaccine after further investigation.
© 2013, Author(s). This open-access article is available under the Creative Commons Attribution 4.0 (CC BY 4.0) International License (https://creativecommons.org/licenses/by/4.0/), which allows for unrestricted use, distribution, and reproduction in any medium, provided that the original work is properly cited.
Siadat SD, Aghasadeghi MR, Karami S, Sadat SM, Moshiri A. Biological and immunological characteristics of Brucella abortus S99 major outer membrane proteins. Jundishapur J Microbiol. 2011;4(1):. doi:
Haghi F, Najar Perayeh S, Siadat SD, Mahdavi M. Cloning, Expression and Purification of Outer Membrane Secretin PilQ406-770 of Neisseria Meningitidis Serogroup B. Arch Clin Infect Dis. 2010;5(4):. doi:
Sam Daliri S, Samadi Kafil H, Aghazadeh M, Fateh A, Yousefi M, et al. Extraction and Biological Evaluation of the Membrane Vesicles of Mycobacterium tuberculosis (CRBIP7.11) as Adjuvant and Vaccine Candidate. Jundishapur J Microbiol. 2017;10(3):e39953. doi: https://doi.org/10.5812/jjm.39953
Davoudi Vijeh Motlagh A, Siadat SD, Abedian Kenari S, Mahdavi M, Behrouzi A, et al. Immunization with Protein D from Non-Typeable Haemophilus influenzae (NTHi) Induced Cytokine Responses and Bioactive Antibody Production. Jundishapur J Microbiol. 2016;9(10):e36617. doi: https://doi.org/10.5812/jjm.36617
Liu X, Chen C, Chen C, Ding R, Marslin G. Construction of a Recombinant OmpC Dominant Epitope-Based Vaccine Against Escherichia coli and Evaluation of Its Immunogenicity and Protective Immunity. Jundishapur J Microbiol. 2017;10(11):e55652. doi: https://doi.org/10.5812/jjm.55652
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