Proteome-wide screening for designing a multi-epitope vaccine against emerging pathogen Elizabethkingia anophelis using immunoinformatic approaches. Issue 16 (1st November 2020)

• Record Type: Journal Article
• Authors: Nain, Zulkar; Abdulla, Faruq; Rahman, M. Mizanur; Karim, Mohammad Minnatul; Khan, Md. Shakil Ahmed; Sayed, Sifat Bin; Mahmud, Shafi; Rahman, S. M. Raihan; Sheam, Md. Moinuddin; Haque, Zahurul; Adhikari, Utpal Kumar
• Is Part Of: Journal of biomolecular structure & dynamics. Volume 38:Issue 16(2020)
• Page Start: 4850
• Page End: 4867
• Publication Date: 2020-11-01
• Subjects: Elizabethkingia anophelis -- immunoinformatics -- multi-epitope vaccine -- dynamics simulation -- immune simulation; Biomolecules -- Periodicals; Molecular structure -- Periodicals; Molecular Biology -- Periodicals; Biomechanics -- Periodicals; 572
• DOI: 10.1080/07391102.2019.1692072
• Languages: English
• ISSNs: 0739-1102

Abstract

Abstract: Elizabethkingia anophelis is an emerging human pathogen causing neonatal meningitis, catheter-associated infections and nosocomial outbreaks with high mortality rates. Besides, they are resistant to most antibiotics used in empirical therapy. In this study, therefore, we used immunoinformatic approaches to design a prophylactic peptide vaccine against E. anophelis as an alternative preventive measure. Initially, cytotoxic T-lymphocyte (CTL), helper T-lymphocyte (HTL), and linear B-lymphocyte (LBL) epitopes were predicted from the highest antigenic protein. The CTL and HTL epitopes together had a population coverage of 99.97% around the world. Eventually, six CTL, seven HTL, and two LBL epitopes were selected and used to construct a multi-epitope vaccine. The vaccine protein was found to be highly immunogenic, non-allergenic, and non-toxic. Codon adaptation and in silico cloning were performed to ensure better expression within E. coli K12 host system. The stability of the vaccine structure was also improved by disulphide bridging. In addition, molecular docking and dynamics simulation revealed strong and stable binding affinity between the vaccine and toll-like receptor 4 (TLR4) molecule. The immune simulation showed higher levels of T-cell and B-cell activities which was in coherence with actual immune response. Repeated exposure simulation resulted in higher clonal selection and faster antigen clearance. Nevertheless, experimental validation is required to ensure the immunogenic potency and safety of this vaccine to control E. anophelis infection in the future. Communicated by Ramaswamy H. Sarma