Recombinant Staphylococcal Antigen-F (r-ScaF), a novel vaccine candidate against methicillin resistant Staphylococcus aureus infection: Potency and efficacy studies
Related Experiment Video
Updated: Feb 1, 2026

Subcutaneous Infection of Methicillin Resistant Staphylococcus Aureus MRSA
Published on: February 9, 2011
Peyman Avakh Majelan1, Mehdi Mahdavi2, Mohammad Hossein Yazdi2
1Department of Pathobiology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
Abstract:
Staphylococcus aureus is a human commensal and pathogen, its clinical importance is exacerbated by the spread of multi-drug resistant strains. The potential future failure of antibiotic therapy necessitates the development of novel control regimes, including new immunotherapeutic approaches. S. aureus has a large repertoire of surface components with potential for immunological targeting. The aim of this study was to evaluate the efficacy of a novel member of staphylococcal conserved antigen family (ScaF) as a factor to elicit cellular and humoral immunity. To determine the ScaF potential as a vaccine candidate, experimental groups of mice were immunized with recombinant Scaf (r-ScaF) formulated in Freund's and alum adjuvants or PBS and subsequently challenged in the sepsis model of S. aureus disease. The vaccine formulations induced robust cellular cytokines responses, including IFN-γ and IL-17, as well as increased production of IgG2a rather than other subclass of IgGs. Active immunization with r-ScaF with adjuvants led to decreased mortality of infected mice and a lower associated bacterial burden in the internal organs in comparison to the control group. Taken together, our Results indicate to the possibility of the r-ScaF protein to be considered as an important component of a multivalent prophylactic vaccine candidate.
Insights
A novel Staphylococcus aureus conserved antigen family (ScaF) protein shows promise as a vaccine candidate. Immunization with recombinant ScaF reduced mortality and bacterial load in mice challenged with S. aureus sepsis.
Area of Science:
- Microbiology
- Immunology
- Vaccinology
Background:
- Staphylococcus aureus poses a significant threat due to multi-drug resistant strains.
- Antibiotic resistance necessitates novel therapeutic strategies, including immunotherapies.
- Surface components of S. aureus are potential targets for immune interventions.
Purpose of the Study:
- To evaluate the efficacy of a novel staphylococcal conserved antigen family (ScaF) protein as a vaccine candidate.
- To assess the ability of recombinant ScaF (r-ScaF) to elicit cellular and humoral immune responses.
- To determine the protective potential of r-ScaF against S. aureus infection.
Main Methods:
- Mice were immunized with r-ScaF formulated with Freund's or alum adjuvants.
- Immunized mice were challenged with S. aureus in a sepsis model.
- Cellular cytokine responses (IFN-γ, IL-17) and antibody production (IgG subclasses) were measured.
- Mortality rates and bacterial burden in internal organs were assessed.
Main Results:
- Vaccine formulations induced robust cellular immune responses, including IFN-γ and IL-17.
- Humoral immunity showed increased production of IgG2a.
- Active immunization with r-ScaF significantly decreased mortality in infected mice.
- A lower bacterial burden was observed in the internal organs of immunized mice compared to controls.
Conclusions:
- Recombinant ScaF (r-ScaF) effectively elicits protective immune responses against S. aureus.
- r-ScaF demonstrates potential as a prophylactic vaccine component.
- This study supports the consideration of r-ScaF in a multivalent vaccine strategy against S. aureus infections.
More Related Videos
07:32Evaluating the Immune Response of a Nanoemulsion Adjuvant Vaccine Against Methicillin-Resistant Staphylococcus aureus MRSA Infection
Published on: September 1, 2023
09:03Multiplex PCR Assay for Typing of Staphylococcal Cassette Chromosome Mec Types I to V in Methicillin-resistant Staphylococcus aureus
Published on: September 5, 2013
Related Concept Videos
Vaccinations
Dose-Response Relationship: Potency and Efficacy
Viral Recombination
Recombinant DNA
Self-Efficacy
Homologous Recombination