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Detection of Neutralization-sensitive Epitopes in Antigens Displayed on Virus-Like Particle VLP-Based Vaccines Using a Capture Assay
Published on: February 10, 2022
Phage vaccines displaying YGKDVKDLFDYAQE epitope induce protection against systemic candidiasis in mouse model
Hongxi Shi1, Shuai Dong2, Xintong Zhang2
1Key Laboratory of Molecular Epigenetics of MOE and Institute of Genetics & Cytology, Northeast Normal University, Changchun, PR China.
Abstract:
Candida albicans is a common commensal and opportunistic fungal pathogen in human, which poses threat to human health, especially in immunocompromised patients. Unfortunately, few effective prophylactic and therapeutic strategies were applied to clinic practice. Recently, the peptide YGKDVKDLFDYAQE from Fructose-bisphosphate aldolase 1 (Fba1), as a vaccine, was reported to induce protection effects against systemic candidiasis. Here, we displayed this epitope peptide on the coat proteins (pIII or pVIII) of filamentous phage, and investigated their protective effects against C. albicans infections. Mice were immunized with recombinant phages (designated as phage-3F and phage-8F) or protein (rFba1), then challenged with C. albicans yeast cells via lateral tail vein. Results demonstrated that the recombinant phages as well as rFba1 apparently induced humoral and cellular immune responses, reduced fungal burden and relieved kidney damage in infected mice and significantly improved their survival rates. Briefly, all these findings indicated that the recombinant phages displaying the epitope YGKDVKDLFDYAQE have the potential to be developed into a new vaccine against C. albicans infections.
Insights
Recombinant phages displaying a peptide from Fructose-bisphosphate aldolase 1 (Fba1) show promise as a novel vaccine. These engineered phages effectively protect against Candida albicans infections in mice, improving survival rates.
Area of Science:
- Mycology
- Immunology
- Vaccine Development
Background:
- Candida albicans is an opportunistic fungal pathogen causing significant health threats, particularly in immunocompromised individuals.
- Current prophylactic and therapeutic strategies against candidiasis are limited.
- A peptide from Fructose-bisphosphate aldolase 1 (Fba1) has shown potential as a vaccine against systemic candidiasis.
Purpose of the Study:
- To display an epitope peptide (YGKDVKDLFDYAQE) from Fba1 on filamentous phage coat proteins (pIII or pVIII).
- To investigate the protective effects of these recombinant phages against Candida albicans infections.
- To evaluate the potential of phage-displayed peptides as a novel vaccine strategy.
Main Methods:
- Epitope peptide YGKDVKDLFDYAQE was displayed on filamentous phage coat proteins (pIII and pVIII).
- Mice were immunized with recombinant phages (phage-3F, phage-8F) or recombinant Fba1 (rFba1).
- Immunized mice were challenged with Candida albicans yeast cells, and immune responses, fungal burden, kidney damage, and survival rates were assessed.
Main Results:
- Recombinant phages and rFba1 successfully induced humoral and cellular immune responses in mice.
- Immunization with recombinant phages significantly reduced fungal burden and kidney damage.
- The developed vaccines markedly improved survival rates in mice challenged with Candida albicans.
Conclusions:
- Recombinant phages displaying the Fba1-derived epitope YGKDVKDLFDYAQE are effective in protecting against Candida albicans infections.
- These engineered phages represent a promising new vaccine candidate for candidiasis.
- Phage display technology offers a viable platform for developing vaccines against fungal pathogens.
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