Reverse vaccinology approach to design a novel multi-epitope subunit vaccine against avian influenza A (H7N9) virus. (May 2019)

• Record Type: Journal Article
• Authors: Hasan, Mahmudul; Ghosh, Progga Paromita; Azim, Kazi Faizul; Mukta, Shamsunnahar; Abir, Ruhshan Ahmed; Nahar, Jannatun; Hasan Khan, Mohammad Mehedi
• Is Part Of: Microbial pathogenesis. Volume 130(2019)
• Page Start: 19
• Page End: 37
• Publication Date: 2019-05
• Subjects: Reverse vaccinology -- Epitope based vaccine -- Avian influenza A(H7N9) -- B- cell immunity -- T-cell immunity; Pathogenic microorganisms -- Periodicals; Pathology, Molecular -- Periodicals; Communicable Diseases -- microbiology -- Periodicals; Communicable Diseases -- parasitology -- Periodicals; Micro-organismes pathogènes -- Périodiques; Pathologie moléculaire -- Périodiques; Electronic journals; 616.9041
• DOI: 10.1016/j.micpath.2019.02.023
• Languages: English
• ISSNs: 0882-4010

Abstract

Abstract: H7N9, a novel strain of avian origin influenza was the first recorded incidence where a human was transited by a N9 type influenza virus. Effective vaccination against influenza A (H7N9) is a major concern, since it has emerged as a life threatening viral pathogen. Here, an in silico reverse vaccinology strategy was adopted to design a unique chimeric subunit vaccine against avian influenza A (H7N9). Induction of humoral and cell-mediated immunity is the prime concerned characteristics for a peptide vaccine candidate, hence both T cell and B cell immunity of viral proteins were screened. Antigenicity testing, transmembrane topology screening, allergenicity and toxicity assessment, population coverage analysis and molecular docking approach were adopted to generate the most antigenic epitopes of avian influenza A (H7N9) proteome. Further, a novel subunit vaccine was designed by the combination of highly immunogenic epitopes along with suitable adjuvant and linkers. Physicochemical properties and secondary structure of the designed vaccine were assessed to ensure its thermostability, h ydrophilicity, theoretical PI and structural behavior. Homology modeling, refinement and validation of the designed vaccine allowed to construct a three dimensional structure of the predicted vaccine, further employed to molecular docking analysis with different MHC molecules and human immune TLR8 receptor present on lymphocyte cells. Moreover, disulfide engineering was employed to lessen the high mobility region of the designed vaccine in order to extend its stability. Furthermore, we investigated the molecular dynamic simulation of the modeled subunit vaccine and TLR8 complexed molecule to strengthen our prediction. Finally, the suggested vaccine was reverse transcribed and adapted for E. coli strain K12 prior to insertion within pET28a(+) vector for checking translational potency and microbial expression. Graphical abstract: Image 1 Highlights: Matrix protein 1 & Hemagglutinin were most antigenic in avian influenza A H7N9 virus. The predicted epitopes displayed high cumulative population coverage and conservancy. Conjugation of the epitopes via linkers resulted in potential vaccine candidates. Designed vaccine was non-allergic; showed lowest binding energy with MHC molecules. The vaccine-TLR8 complex was structurally stable to confer strong immune response.