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Immune responses to epitopes inserted in Salmonella flagellin
1Department of Microbiology and Immunology, Stanford University School of Medicine, CA 94305-5402.
International Reviews of Immunology
|January 1, 1994
Summary
This study engineered chimeric flagellins using Salmonella flagellin and foreign epitopes. These engineered flagellins, when expressed in live vaccines, successfully presented foreign epitopes on flagella, eliciting immune responses in mice.
Area of Science:
- Molecular Biology
- Vaccinology
- Immunology
Background:
- Plasmid pLS408 contains the Salmonella flagellin gene (fliC) with a modified antigenically-determinant region.
- Engineering chimeric flagellins allows for the display of foreign epitopes on bacterial flagella.
Purpose of the Study:
- To investigate the production of chimeric flagellins with foreign peptide epitopes inserted into Salmonella flagellin.
- To assess the immunogenicity and potential protective effects of these chimeric flagellins in a live vaccine system.
Main Methods:
- Insertion of synthetic oligonucleotides encoding foreign peptide epitopes into the EcoRV site of pLS408.
- Expression of chimeric flagellins in a flagellin-deficient Salmonella dublin live-vaccine strain.
- Immunization of mice with the engineered live vaccine or semi-purified chimeric flagella/flagellin.
- Analysis of antibody production and protective immunity against pathogen challenge.
Main Results:
- Chimeric flagellins were produced, displaying foreign epitopes on the surface of functional flagella.
- Administration of the live vaccine induced antibodies specific for the foreign epitopes.
- Partial protection against Streptococcus and influenza A virus challenge was observed following immunization.
Conclusions:
- Chimeric flagellins can be successfully engineered to display foreign epitopes, serving as a platform for vaccine development.
- The live Salmonella vaccine system effectively presents these chimeric antigens, eliciting humoral immune responses.
- Further research is needed to understand factors influencing functional flagella production and cellular immune responses.