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MTBVeb: A Web-Based Platform for Designing Vaccines against Existing and Emerging Strains of Mycobacterium tuberculosis

Overview

MTBVeb is a web-based computational platform developed for designing vaccines against existing and emerging strains of Mycobacterium tuberculosis (Mtb).

The platform integrates:

  • Comparative genomics
  • Antigen prediction
  • Epitope prediction
  • Vaccine candidate identification
  • Strain-specific analysis

MTBVeb assists researchers in designing:

  • Strain-based vaccines
  • Antigen-based vaccines
  • Epitope-based vaccines

against drug-sensitive and drug-resistant strains of Mycobacterium tuberculosis.


Research Paper Details

Title

A Web-Based Platform for Designing Vaccines against Existing and Emerging Strains of Mycobacterium tuberculosis

Authors

  • Sandeep Kumar Dhanda
  • Pooja Vir
  • Deepak Singla
  • Sudheer Gupta
  • Shailesh Kumar
  • Gajendra P. S. Raghava

Journal

PLoS ONE

Volume

11

Issue

4

Article Number

e0153771

Published Date

20 April 2016

Correct DOI

Background

Tuberculosis remains one of the deadliest infectious diseases worldwide.

Major challenges include:

  • Drug-resistant tuberculosis strains
  • Limited efficacy of BCG vaccine in adults
  • Emerging multidrug-resistant strains
  • Lack of effective universal vaccines

Modern technologies such as:

  • Next Generation Sequencing (NGS)
  • Immunoinformatics
  • Epitope prediction
  • Comparative genomics

can help accelerate vaccine development against emerging Mtb strains.

MTBVeb was developed to address these challenges using computational approaches.


Objectives

The study aimed to:

  • Develop a comprehensive vaccine design platform
  • Analyze multiple Mtb strains
  • Identify antigenic vaccine candidates
  • Predict B-cell and T-cell epitopes
  • Support vaccine design against newly sequenced strains
  • Integrate genome analysis and epitope prediction tools

Strain Dataset

The study analyzed:

Strain Category Number
Tuberculoid strains 23
Vaccine strains 5
Non-tuberculoid strains 30
Total strains 59

These included:

  • Drug-sensitive strains
  • Drug-resistant strains
  • Clinical isolates
  • Laboratory strains
  • BCG vaccine variants

Vaccine Candidate Identification

A total of:

  • 178 vaccine candidates
  • 166 unique proteins

were identified from literature and previous studies.

Categories of Vaccine Candidates

1. Virulence Associated Proteins

  • 125 proteins

2. Secretion System Components

  • 20 proteins

3. Regions of Deletion (RD) Proteins

  • 33 proteins

These proteins were analyzed across all strains using sequence similarity search.


Comparative Genomics Analysis

The platform compared vaccine candidate proteins across different Mtb strains.

Key Findings

  • Virulent and secretory proteins differentiate pathogenic and non-pathogenic strains
  • RD proteins differentiate vaccine strains from pathogenic strains
  • Many vaccine candidates are membrane or extracellular proteins

Epitope Prediction Pipeline

The study generated overlapping 9-mer peptides from vaccine candidate proteins.

Total Unique Peptides

Description Count
Unique 9-mer peptides 103,522

Predicted Immune Components

Immune Feature Count
B-cell epitopes 8,292
MHC Class I binders 46,484
CTL epitopes 34,922
MHC Class II binders 14,907
Th1 epitopes 6,242
Th2 epitopes 9,720

Experimentally Validated Epitopes

Experimentally validated epitopes were obtained from:

  • Immune Epitope Database (IEDB)

Mapped Epitopes

Epitope Type Unique Peptides
B-cell epitopes 659
T-cell epitopes 1,806
MHC binders 1,208

Most validated epitopes mapped to vaccine candidate proteins.


Immunoinformatics Tools Integrated

The platform integrated several prediction tools:

Tool Purpose
LBtope B-cell epitope prediction
Propred MHC Class II prediction
Propred1 MHC Class I prediction
CTLpred CTL epitope prediction
IFNepitope IFN-gamma epitope prediction
IL4pred IL-4 inducing peptide prediction

Database Architecture

The database organizes information into:

  • Strains
  • Antigens
  • Epitopes

Technologies Used

Backend

  • MySQL
  • PHP 5.2.9

Frontend

  • HTML
  • JavaScript

Server

  • Apache HTTP Server 2.2
  • Linux Operating System

Web Server Features

1. Strain-Specific Analysis

Allows users to:

  • Compare strains
  • Analyze newly sequenced genomes
  • Identify conserved regions
  • Visualize genomes

Integrated genome browsers:

  • JBrowse
  • CGView
  • Argo

2. Antigen-Based Vaccine Design

Users can:

  • Browse vaccine candidates
  • Compare vaccine targets
  • Perform similarity searches
  • Map epitopes on antigens

3. Epitope-Based Vaccine Design

Users can:

  • Predict B-cell epitopes
  • Predict T-cell epitopes
  • Perform advanced epitope search
  • Identify epitopes with desired immune responses

Important Findings

The study demonstrated that:

  • Comparative genomics can assist vaccine design
  • RD proteins help differentiate vaccine strains
  • Immunoinformatics pipelines effectively identify vaccine epitopes
  • Large-scale epitope prediction can support subunit vaccine design
  • MTBVeb provides more integrated functionality than existing TB vaccine resources

Comparison with Existing Resources

Compared with other TB vaccine databases, MTBVeb provides:

  • Strain-specific analysis
  • Experimental epitope mapping
  • User strain analysis
  • Epitope prediction pipelines
  • Vaccine strain comparison

Applications

MTBVeb can be used for:

  • Tuberculosis vaccine development
  • Drug-resistant strain analysis
  • Epitope vaccine design
  • Comparative genomics
  • Immunoinformatics
  • Antigen discovery
  • Host-pathogen interaction studies

Web Server

http://crdd.osdd.net/raghava/mtbveb/


Citation

Dhanda SK, Vir P, Singla D, Gupta S, Kumar S, Raghava GPS.

A Web-Based Platform for Designing Vaccines against Existing and Emerging Strains of Mycobacterium tuberculosis.

PLoS ONE. 2016;11(4):e0153771.

DOI: https://doi.org/10.1371/journal.pone.0153771


Contact

Dr. G. P. S. Raghava

Email: raghava@iiitd.ac.in

Address:
Indraprastha Institute of Information Technology Delhi


License

This project/documentation is intended for academic and research purposes only.

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