Comprehensive genome based analysis of Vibrio parahaemolyticus for identifying novel drug and vaccine molecules: Subtractive proteomics and vaccinomics approach.
Mahmudul HasanKazi Faizul AzimMd Abdus Shukur ImranIshtiak Malique ChowdhuryShah Rucksana Akhter UrmeMd Sorwer Alam ParvezMd Bashir UddinSyed Sayeem Uddin AhmedPublished in: PloS one (2020)
Multidrug-resistant Vibrio parahaemolyticus has become a significant public health concern. The development of effective drugs and vaccines against Vibrio parahaemolyticus is the current research priority. Thus, we aimed to find out effective drug and vaccine targets using a comprehensive genome-based analysis. A total of 4822 proteins were screened from V. parahaemolyticus proteome. Among 16 novel cytoplasmic proteins, 'VIBPA Type II secretion system protein L' and 'VIBPA Putative fimbrial protein Z' were subjected to molecular docking with 350 human metabolites, which revealed that Eliglustat, Simvastatin and Hydroxocobalamin were the top drug molecules considering free binding energy. On the contrary, 'Sensor histidine protein kinase UhpB' and 'Flagellar hook-associated protein of 25 novel membrane proteins were subjected to T-cell and B-cell epitope prediction, antigenicity testing, transmembrane topology screening, allergenicity and toxicity assessment, population coverage analysis and molecular docking analysis to generate the most immunogenic epitopes. Three subunit vaccines were constructed by the combination of highly antigenic epitopes along with suitable adjuvant, PADRE sequence and linkers. The designed vaccine constructs (V1, V2, V3) were analyzed by their physiochemical properties and molecular docking with MHC molecules- results suggested that the V1 is superior. Besides, the binding affinity of human TLR-1/2 heterodimer and construct V1 could be biologically significant in the development of the vaccine repertoire. The vaccine-receptor complex exhibited deformability at a minimum level that also strengthened our prediction. The optimized codons of the designed construct was cloned into pET28a(+) vector of E. coli strain K12. However, the predicted drug molecules and vaccine constructs could be further studied using model animals to combat V. parahaemolyticus associated infections.
Keyphrases
- molecular docking
- molecular dynamics simulations
- public health
- endothelial cells
- multidrug resistant
- binding protein
- mass spectrometry
- early stage
- escherichia coli
- immune response
- dna methylation
- oxidative stress
- staphylococcus aureus
- adverse drug
- emergency department
- wastewater treatment
- induced pluripotent stem cells
- small molecule
- drug resistant
- acinetobacter baumannii
- health insurance
- monoclonal antibody
- dna binding
- transcription factor
- capillary electrophoresis
- protein protein