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Updated: Jun 24, 2026

A Murine Model of Group B Streptococcus Vaginal Colonization
Published on: November 16, 2016
Development and evaluation of a multi-epitope subunit vaccine against group B Streptococcus infection
Yumin Zhang1,2,3,4, Song Liang1,2,3,4, Shiyu Zhang1,2,3,4
1College of Veterinary Medicine, Nanjing Agricultural University, Nanjing, People's Republic of China.
Insights
A novel multivalent multiepitope-based subunit vaccine (MVSA) shows 100% protection against Group B Streptococcus (GBS) infection in mice. This GBS vaccine candidate effectively elicits strong immune responses and offers potential for widespread use.
Area of Science:
- Immunology
- Vaccinology
- Microbial Pathogenesis
Background:
- Group B Streptococcus (GBS) is a significant multi-host pathogen, posing life-threatening risks, particularly to newborns.
- Vaccination strategies targeting multiple GBS serotypes are crucial for effective long-term infection control.
- Developing a broadly protective GBS vaccine remains a public health priority.
Purpose of the Study:
- To design and evaluate a novel multivalent multiepitope-based subunit vaccine (MVSA) against Group B Streptococcus (GBS).
- To assess the immunogenicity and protective efficacy of MVSA through in silico and in vivo studies.
- To explore the potential of MVSA for broad population coverage against diverse GBS serotypes.
Main Methods:
- Development of a comprehensive in silico epitope-prediction workflow to identify vaccine candidates.
- Selection of 11 epitopes from confirmed antigenic, virulent-associated, surface-exposed, and conserved GBS proteins across ten serotypes.
- Validation of MVSA efficacy using a mouse model, including antibody titration, splenocyte proliferation assays, and lethal-dose challenge studies.
- In vitro assessment of polyclonal antibodies against MVSA for growth inhibition of multiple GBS serotypes and passive protection assays.
Main Results:
- In silico analysis predicted MVSA's potential to induce strong immune responses and achieve worldwide population coverage.
- Immunization with MVSA in mice resulted in high antibody titers and significant splenocyte proliferation.
- MVSA demonstrated 100% protection against lethal GBS challenge in mice after three vaccinations.
- Polyclonal antibodies against MVSA inhibited GBS growth in vitro across six key serotypes and provided 100% protection in naive mice against lethal GBS challenge.
Conclusions:
- The multivalent multiepitope-based subunit vaccine (MVSA) is a promising candidate for an efficacious GBS vaccine.
- Both active immunization with MVSA and passive immunity conferred by its antibodies provide robust protection against GBS.
- MVSA's ability to target multiple serotypes and induce strong immune responses suggests its potential for broad clinical application against GBS infections.
Abstract:
Streptococcus agalactiae (Group B Streptococcus, GBS) is a multi-host pathogen, even causing life-threatening infections in newborns. Vaccination with GBS crossed serotypes vaccine is one of the best options for long-term infection control. Here we built a comprehensive in silico epitope-prediction workflow pipeline to design a multivalent multiepitope-based subunit vaccine containing 11 epitopes against (MVSA). All epitopes in MVSA came from the proteins which were antigenic-confirmed, virulent-associated, surface-exposed and conserved in ten GBS serotypes. The in-silico analysis showed MVSA had potential to evoke strong immune responses and enable worldwide population coverage. To validate MVSA protection efficacy against GBS infection, immune protection experiments were performed in a mouse model. Importantly, MVSA induced a high titre of antibodies, significant proliferation of mice splenocytes and elicited strong protection against lethal-dose challenge with a survival rate of 100% in mice after three vaccinations. Meanwhile, the polyclonal antibody against MVSA did not only inhibit for growth of GBS from six crucial serotypes in vitro, but also protect 100% naive mice from GBS lethal challenge. These active and passive immunity assay results suggested that MVSA could therefore be an efficacious multi-epitope vaccine against GBS infection.
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