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The immunogenicity of the liposome-associated outer membrane proteins (OMPs) of Moraxella catarrhalis
Daria Augustyniak1, Józef Mleczko, Jan Gutowicz
1Laboratory of Immunology, Institute of Genetics and Microbiology, University of Wrocław, Przybyszewskiego 63/77, 51-148 Wrocław, Poland. august@microb.uni.wroc.pl
Abstract:
The outer membrane proteins (OMPs) are the most immunogenic and attractive of the Moraxella catarrhalis vaccine antigens that may induce the protective immune response. The aim of this study was to determine the effectiveness of two types of OMP-associated phosphatidylcholine (PC) liposomal formulations (OMPs-PC, PC-OMPs) and of Zwittergent-based proteomicelles (OMPs-Z) in potentiating an anti-OMP systemic immune response in mice. The immunogenicities of the above preparations were evaluated by assessing serum anti-OMP IgG and IgA reactivity in the post-immunized mouse antisera using ELISA and Western blotting. Additionally, the cross-reactivity of the most effective anti-OMP response was determined using heterologous sera from both humans and mice. Both the proteoliposomes and the proteomicelles showed high immunogenic properties and did not elicit any distinct quantitative differences in the antibody titer or qualitative differences in the pattern of the mouse antisera. The post-immunized mouse antisera predominantly recognized a approximately 60-kDa OMP of M. catarrhalis. That protein was also found to be a highly cross-reactive antigen interacting with a panel of pooled mouse antisera produced by immunization either with whole cells or the purified OMPs of heterologous M. catarrhalis strains. Furthermore, normal sera collected from healthy children were found to be preferentially reactive with the 60-kDa OMP. The serum-specific IgG, IgA and IgM were respectively detected via immunoblotting in 90%, 85% and 30% of heterologous human sera. This similar immunogenic effectiveness of both OMP-associated liposomal formulations could contribute to the practical use of such formulations in the future in human vaccination. Moreover, the highly cross-reactive 60-kDa OMP seems to be an important antigenic marker of M. catarrhalis, and, as it is responsible for the induction of an antibody-mediated and long-lasting immune response, studying it may partially aid us in understanding the relatively low degree of pathogenicity of the bacterium in immunocompetent individuals.
Insights
Outer membrane proteins (OMPs) from Moraxella catarrhalis, formulated in liposomes or proteomicelles, effectively stimulate anti-OMP immune responses in mice. A 60-kDa OMP was identified as a key cross-reactive antigen in both mice and humans.
Area of Science:
- Immunology
- Vaccinology
- Microbiology
Background:
- Outer membrane proteins (OMPs) of Moraxella catarrhalis are key vaccine targets due to their immunogenicity.
- Developing effective vaccine formulations is crucial for inducing protective immune responses against M. catarrhalis.
Purpose of the Study:
- To evaluate the immunogenic effectiveness of two OMP-associated liposomal formulations (OMPs-PC, PC-OMPs) and Zwittergent-based proteomicelles (OMPs-Z) in mice.
- To identify cross-reactive antigens and assess their potential as vaccine candidates.
Main Methods:
- Immunization of mice with OMP formulations.
- ELISA and Western blotting to assess serum anti-OMP IgG and IgA reactivity.
- Cross-reactivity analysis using human and mouse sera against M. catarrhalis antigens.
Main Results:
- Both liposomal formulations and proteomicelles demonstrated high immunogenic properties.
- A conserved 60-kDa OMP was predominantly recognized by mouse antisera and showed high cross-reactivity.
- This 60-kDa OMP was also reactive with normal human sera from children.
Conclusions:
- OMP-associated liposomal formulations and proteomicelles exhibit similar immunogenic effectiveness for M. catarrhalis vaccines.
- The 60-kDa OMP is a significant cross-reactive antigen and a potential marker for M. catarrhalis.
- Further study of this OMP could aid in understanding M. catarrhalis pathogenicity and vaccine development.
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