4.7 Article

Development of a Conserved Chimeric Vaccine for Induction of Strong Immune Response against Staphylococcus aureus Using Immunoinformatics Approaches

期刊

VACCINES
卷 9, 期 9, 页码 -

出版社

MDPI
DOI: 10.3390/vaccines9091038

关键词

Staphylococcus aureus; SdrD; SdrE; immunoinformatics; multi-epitope vaccine

资金

  1. DBT-BUILDER program at KIIT Deemed to Be University, Bhubaneswar [BT/INF/22/SP42155/2021]
  2. National Research Foundation of Korea (NRF) - Korean government (MSIT) [2020R1A2C2004128]
  3. Korea Basic Science Institute (National Research Facilities and Equipment Center) - Ministry of Education [2020R1A6C101A188]
  4. National Research Foundation of Korea [2020R1A2C2004128, 2020R1A6C101A188] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

Staphylococcus aureus is a highly deadly Gram-positive bacterium that poses a major challenge for vaccine development. The novel vaccine candidate constructed using immunoinformatics approach shows promising immune response in worldwide populations. This chimeric vaccine has the potential to elicit both humoral and cell-mediated immune responses against the multidrug-resistant pathogen.
Staphylococcus aureus is one of the most notorious Gram-positive bacteria with a very high mortality rate. The WHO has listed S. aureus as one of the ESKAPE pathogens requiring urgent research and development efforts to fight against it. Yet there is a major layback in the advancement of effective vaccines against this multidrug-resistant pathogen. SdrD and SdrE proteins are attractive immunogen candidates as they are conserved among all the strains and contribute specifically to bacterial adherence to the host cells. Furthermore, these proteins are predicted to be highly antigenic and essential for pathogen survival. Therefore, in this study, using the immunoinformatics approach, a novel vaccine candidate was constructed using highly immunogenic conserved T-cell and B-cell epitopes along with specific linkers, adjuvants, and consequently modeled for docking with human Toll-like receptor 2. Additionally, physicochemical properties, secondary structure, disulphide engineering, and population coverage analysis were also analyzed for the vaccine. The constructed vaccine showed good results of worldwide population coverage and a promising immune response. For evaluation of the stability of the vaccine-TLR-2 docked complex, a molecular dynamics simulation was performed. The constructed vaccine was subjected to in silico immune simulations by C-ImmSim and Immune simulation significantly provided high levels of immunoglobulins, T-helper cells, T-cytotoxic cells, and INF-gamma. Lastly, upon cloning, the vaccine protein was reverse transcribed into a DNA sequence and cloned into a pET28a (+) vector to ensure translational potency and microbial expression. The overall results of the study showed that the designed novel chimeric vaccine can simultaneously elicit humoral and cell-mediated immune responses and is a reliable construct for subsequent in vivo and in vitro studies against the pathogen.

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