4.4 Article

Designing a novel multi-epitope vaccine to evoke a robust immune response against pathogenic multidrug-resistant Enterococcus faecium bacterium

Journal

GUT PATHOGENS
Volume 14, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s13099-022-00495-z

Keywords

Enterococcus faecium; Penicillin-binding protein; Vaccine; Epitope; Immunoinformatics

Funding

  1. DBT-BUILDER program at KIIT Deemed to Be University, Bhubaneswar [BT/INF/22/SP42155/2021]

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This study aimed to design a novel vaccine against Enterococcus faecium using immunoinformatics approaches. Through in-depth analysis, suitable epitopes were selected for vaccine development. The constructed vaccine showed high immunogenicity and stability. Immune simulation results indicated a strong immune response, making it a promising target.
Enterococcus faecium is an emerging ESKAPE bacterium that is capable of causing severe public health complications in humans. There are currently no licensed treatments or vaccinations to combat the deadly pathogen. We aimed to design a potent and novel prophylactic chimeric vaccine against E. faecium through an immunoinformatics approach The antigenic Penicillin-binding protein 5 (PBP 5) protein was selected to identify B and T cell epitopes, followed by conservancy analysis, population coverage, physiochemical assessment, secondary and tertiary structural analysis. Using various immunoinformatics methods and tools, two linear B-cell epitopes, five CTL epitopes, and two HTL epitopes were finally selected for vaccine development. The constructed vaccine was determined to be highly immunogenic, cytokine-producing, antigenic, non-toxic, non-allergenic, and stable, as well as potentially effective against E. faecium. In addition, disulfide engineering, codon adaptation, and in silico cloning, were used to improve stability and expression efficiency in the host E. coli. Molecular docking and molecular dynamics simulations indicated that the structure of the vaccine is stable and has a high affinity for the TLR4 receptor. The immune simulation results revealed that both B and T cells had an increased response to the vaccination component. Conclusively, the in-depth in silico analysis suggests, the proposed vaccine to elicit a robust immune response against E. faecium infection and hence a promising target for further experimental trials.

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