Abstract

The identification of protective immunogens is the most important and vigorous initial step in the long-lasting and expensive process of vaccine design and development. Machine learning (ML) methods are very effective in data mining and in the analysis of big data such as microbial proteomes. They are able to significantly reduce the experimental work for discovering novel vaccine candidates. Here, we applied six supervised ML methods (partial least squares-based discriminant analysis, k nearest neighbor (kNN), random forest (RF), support vector machine (SVM), random subspace method (RSM), and extreme gradient boosting) on a set of 317 known bacterial immunogens and 317 bacterial non-immunogens and derived models for immunogenicity prediction. The models were validated by internal cross-validation in 10 groups from the training set and by the external test set. All of them showed good predictive ability, but the xgboost model displays the most prominent ability to identify immunogens by recognizing 84% of the known immunogens in the test set. The combined RSM-kNN model was the best in the recognition of non-immunogens, identifying 92% of them in the test set. The three best performing ML models (xgboost, RSM-kNN, and RF) were implemented in the new version of the server VaxiJen, and the prediction of bacterial immunogens is now based on majority voting.

Highlights

  • IntroductionImmunogenicity is the ability of a foreign biomacromolecule (protein, lipid, carbohydrate, or a combination of them) to produce a humoral and/or cell-mediated immune response in the host organism

  • Immunogenicity is the ability of a foreign biomacromolecule to produce a humoral and/or cell-mediated immune response in the host organism

  • The three best performing machine learning (ML) models were implemented in the new version of the server VaxiJen, and the prediction of bacterial immunogens is based on majority voting

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Summary

Introduction

Immunogenicity is the ability of a foreign biomacromolecule (protein, lipid, carbohydrate, or a combination of them) to produce a humoral and/or cell-mediated immune response in the host organism. Protective immunogens of pathogenic origin are perspective vaccine candidates [1]. During the last ten years, several approaches for immunogenicity prediction of whole protein antigens have been developed [3]. Most of them like NERVE [4], Vaxign [5], ANTIGENpro, Vacceed [6], Jenner-predict [7], iVAX [8], VacSol [9], and Protectome analysis [10] work as a series of filters selecting the most probable vaccine candidates such as filters that utilize subcellular localization, adhesion probability, topology, sequence similarity with human proteins, etc

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