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Bacterial Outer Membrane Vesicles (OMVs)-based Dual Vaccine for Influenza A H1N1 Virus and MERS-CoV
Mahmoud M Shehata1, Ahmed Mostafa2,3, Lisa Teubner4
1Center of Scientific Excellence for Influenza Viruses, Environmental Research Division, National Research Centre (NRC), Cairo 12622, Egypt. Mahmoud.Shehata@human-link.org.
Abstract:
Vaccination is the most functional medical intervention to prophylactically control severe diseases caused by human-to-human or animal-to-human transmissible viral pathogens. Annually, seasonal influenza epidemics attack human populations leading to 290-650 thousand deaths/year worldwide. Recently, a novel Middle East Respiratory Syndrome Coronavirus emerged. Together, those two viruses present a significant public health burden in areas where they circulate. Herein, we generated a bacterial outer membrane vesicles (OMVs)-based vaccine presenting the antigenic stable chimeric fusion protein of the H1-type haemagglutinin (HA) of the pandemic influenza A virus (H1N1) strain from 2009 (H1N1pdm09) and the receptor binding domain (RBD) of the Middle East Respiratory Syndrome Coronavirus (MERS-CoV) (OMVs-H1/RBD). Our results showed that the chimeric antigen could induce specific neutralizing antibodies against both strains leading to protection of immunized mice against H1N1pdm09 and efficient neutralization of MERS-CoV. This study demonstrate that OMVs-based vaccines presenting viral antigens provide a safe and reliable approach to protect against two different viral infections.
Insights
A novel vaccine using bacterial outer membrane vesicles (OMVs) presents a fusion of influenza (H1N1pdm09) and MERS-CoV antigens. This OMV-based vaccine successfully induced protective antibodies against both viruses in mice.
Area of Science:
- Vaccinology
- Virology
- Microbiology
Background:
- Seasonal influenza and Middle East Respiratory Syndrome Coronavirus (MERS-CoV) pose significant global health threats.
- Vaccination is a critical intervention for controlling severe viral diseases.
- Developing effective vaccines against multiple pathogens is a public health priority.
Purpose of the Study:
- To develop and evaluate a novel vaccine platform for simultaneous protection against influenza and MERS-CoV.
- To assess the immunogenicity and protective efficacy of a chimeric antigen-based vaccine.
Main Methods:
- Generation of bacterial outer membrane vesicles (OMVs) displaying a chimeric fusion protein.
- The fusion protein combined the H1-type haemagglutinin (HA) of pandemic influenza A virus (H1N1pdm09) and the receptor binding domain (RBD) of MERS-CoV.
- Immunization of mice with the OMV-based vaccine (OMVs-H1/RBD) and subsequent challenge studies.
Main Results:
- The chimeric antigen (H1/RBD) successfully induced specific neutralizing antibodies against both H1N1pdm09 and MERS-CoV.
- Immunized mice were protected against H1N1pdm09 challenge.
- The vaccine demonstrated efficient neutralization of MERS-CoV.
Conclusions:
- Bacterial outer membrane vesicles (OMVs) serve as a viable platform for developing multi-valent vaccines.
- OMVs-based vaccines presenting viral antigens offer a safe and effective approach for protection against diverse viral infections.
- This strategy holds promise for addressing the public health burden of influenza and emerging coronaviruses.
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