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Development of Innovative Multi-epitope MRNA Vaccine Against Pseudomonas Aeruginosa Using in Silico Approaches

Overview
Journal Brief Bioinform
Specialty Biology
Date 2024 Jan 8
PMID 38189537
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Abstract

The rising issue of antibiotic resistance has made treating Pseudomonas aeruginosa infections increasingly challenging. Therefore, vaccines have emerged as a viable alternative to antibiotics for preventing P. aeruginosa infections in susceptible individuals. With its superior accuracy, high efficiency in stimulating cellular and humoral immune responses, and low cost, mRNA vaccine technology is quickly replacing traditional methods. This study aimed to design a novel mRNA vaccine by using in silico approaches against P. aeruginosa. The research team identified five surface and antigenic proteins and selected their appropriate epitopes with immunoinformatic tools. These epitopes were then examined for toxicity, allergenicity and homology. The researchers also checked their presentation and identification by major histocompatibility complex cells and other immune cells through valuable tools like molecular docking. They subsequently modeled a multi-epitope protein and optimized it. The mRNA was analyzed in terms of structure and stability, after which the immune system's response against the new vaccine was simulated. The results indicated that the designed mRNA construct could be an effective and promising vaccine that requires laboratory and clinical trials.

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References
1.
Huang W, Hamouche J, Wang G, Smith M, Yin C, Dhand A . Integrated Genome-Wide Analysis of an Isogenic Pair of Clinical Isolates with Differential Antimicrobial Resistance to Ceftolozane/Tazobactam, Ceftazidime/Avibactam, and Piperacillin/Tazobactam. Int J Mol Sci. 2020; 21(3). PMC: 7037351. DOI: 10.3390/ijms21031026. View

2.
Worgall S . 40 years on: have we finally got a vaccine for Pseudomonas aeruginosa?. Future Microbiol. 2012; 7(12):1333-5. DOI: 10.2217/fmb.12.106. View

3.
Faezi S, Bahrmand A, Mahdavi M, Siadat S, Nikokar I, Sardari S . Development of a Novel Anti-Adhesive Vaccine Against Targeting the C-terminal Disulfide Loop of the Pilin Protein. Int J Mol Cell Med. 2017; 6(2):96-108. PMC: 5581551. DOI: 10.22088/acadpub.BUMS.6.2.4. View

4.
Zadeh R, Mirshekar M, Kalani B, Pourghader J, Barati M, Masjedian Jazi F . The expression of type II TA system genes following persister cell formation in Pseudomonas aeruginosa isolates in the exponential and stationary phases. Arch Microbiol. 2022; 204(8):451. DOI: 10.1007/s00203-022-03038-x. View

5.
Song W, Yoon S . Crystal structure of FliC flagellin from Pseudomonas aeruginosa and its implication in TLR5 binding and formation of the flagellar filament. Biochem Biophys Res Commun. 2014; 444(2):109-15. DOI: 10.1016/j.bbrc.2014.01.008. View