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Pan-Genome Analysis of Oral Bacterial Pathogens to Predict a Potential Novel Multi-Epitopes Vaccine Candidate

Porphyromonas gingivalis is a Gram-negative anaerobic bacterium, mainly present in the oral cavity and causes periodontal infections. Currently, no licensed vaccine is available against P. gingivalis and other oral bacterial pathogens. To develop a vaccine against P. gingivalis, herein, we applied a...

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Autores principales: Rida, Tehniyat, Ahmad, Sajjad, Ullah, Asad, Ismail, Saba, Tahir ul Qamar, Muhammad, Afsheen, Zobia, Khurram, Muhammad, Saqib Ishaq, Muhammad, Alkhathami, Ali G., Alatawi, Eid A., Alrumaihi, Faris, Allemailem, Khaled S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9320593/
https://www.ncbi.nlm.nih.gov/pubmed/35886259
http://dx.doi.org/10.3390/ijerph19148408
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author Rida, Tehniyat
Ahmad, Sajjad
Ullah, Asad
Ismail, Saba
Tahir ul Qamar, Muhammad
Afsheen, Zobia
Khurram, Muhammad
Saqib Ishaq, Muhammad
Alkhathami, Ali G.
Alatawi, Eid A.
Alrumaihi, Faris
Allemailem, Khaled S.
author_facet Rida, Tehniyat
Ahmad, Sajjad
Ullah, Asad
Ismail, Saba
Tahir ul Qamar, Muhammad
Afsheen, Zobia
Khurram, Muhammad
Saqib Ishaq, Muhammad
Alkhathami, Ali G.
Alatawi, Eid A.
Alrumaihi, Faris
Allemailem, Khaled S.
author_sort Rida, Tehniyat
collection PubMed
description Porphyromonas gingivalis is a Gram-negative anaerobic bacterium, mainly present in the oral cavity and causes periodontal infections. Currently, no licensed vaccine is available against P. gingivalis and other oral bacterial pathogens. To develop a vaccine against P. gingivalis, herein, we applied a bacterial pan-genome analysis (BPGA) on the bacterial genomes that retrieved a total number of 4908 core proteins, which were further utilized for the identification of good vaccine candidates. After several vaccine candidacy analyses, three proteins, namely lytic transglycosylase domain-containing protein, FKBP-type peptidyl-propyl cis-trans isomerase and superoxide dismutase, were shortlisted for epitopes prediction. In the epitopes prediction phase, different types of B and T-cell epitopes were predicted and only those with an antigenic, immunogenic, non-allergenic, and non-toxic profile were selected. Moreover, all the predicted epitopes were joined with each other to make a multi-epitopes vaccine construct, which was linked further to the cholera toxin B-subunit to enhance the antigenicity of the vaccine. For downward analysis, a three dimensional structure of the designed vaccine was modeled. The modeled structure was checked for binding potency with major histocompatibility complex I (MHC-I), major histocompatibility complex II (MHC-II), and Toll-like receptor 4 (TLR-4) immune cell receptors which revealed that the designed vaccine performed proper binding with respect to immune cell receptors. Additionally, the binding efficacy of the vaccine was validated through a molecular dynamic simulation that interpreted strong intermolecular vaccine–receptor binding and confirmed the exposed situation of vaccine epitopes to the host immune system. In conclusion, the study suggested that the model vaccine construct has the potency to generate protective host immune responses and that it might be a good vaccine candidate for experimental in vivo and in vitro studies.
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spelling pubmed-93205932022-07-27 Pan-Genome Analysis of Oral Bacterial Pathogens to Predict a Potential Novel Multi-Epitopes Vaccine Candidate Rida, Tehniyat Ahmad, Sajjad Ullah, Asad Ismail, Saba Tahir ul Qamar, Muhammad Afsheen, Zobia Khurram, Muhammad Saqib Ishaq, Muhammad Alkhathami, Ali G. Alatawi, Eid A. Alrumaihi, Faris Allemailem, Khaled S. Int J Environ Res Public Health Article Porphyromonas gingivalis is a Gram-negative anaerobic bacterium, mainly present in the oral cavity and causes periodontal infections. Currently, no licensed vaccine is available against P. gingivalis and other oral bacterial pathogens. To develop a vaccine against P. gingivalis, herein, we applied a bacterial pan-genome analysis (BPGA) on the bacterial genomes that retrieved a total number of 4908 core proteins, which were further utilized for the identification of good vaccine candidates. After several vaccine candidacy analyses, three proteins, namely lytic transglycosylase domain-containing protein, FKBP-type peptidyl-propyl cis-trans isomerase and superoxide dismutase, were shortlisted for epitopes prediction. In the epitopes prediction phase, different types of B and T-cell epitopes were predicted and only those with an antigenic, immunogenic, non-allergenic, and non-toxic profile were selected. Moreover, all the predicted epitopes were joined with each other to make a multi-epitopes vaccine construct, which was linked further to the cholera toxin B-subunit to enhance the antigenicity of the vaccine. For downward analysis, a three dimensional structure of the designed vaccine was modeled. The modeled structure was checked for binding potency with major histocompatibility complex I (MHC-I), major histocompatibility complex II (MHC-II), and Toll-like receptor 4 (TLR-4) immune cell receptors which revealed that the designed vaccine performed proper binding with respect to immune cell receptors. Additionally, the binding efficacy of the vaccine was validated through a molecular dynamic simulation that interpreted strong intermolecular vaccine–receptor binding and confirmed the exposed situation of vaccine epitopes to the host immune system. In conclusion, the study suggested that the model vaccine construct has the potency to generate protective host immune responses and that it might be a good vaccine candidate for experimental in vivo and in vitro studies. MDPI 2022-07-09 /pmc/articles/PMC9320593/ /pubmed/35886259 http://dx.doi.org/10.3390/ijerph19148408 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Rida, Tehniyat
Ahmad, Sajjad
Ullah, Asad
Ismail, Saba
Tahir ul Qamar, Muhammad
Afsheen, Zobia
Khurram, Muhammad
Saqib Ishaq, Muhammad
Alkhathami, Ali G.
Alatawi, Eid A.
Alrumaihi, Faris
Allemailem, Khaled S.
Pan-Genome Analysis of Oral Bacterial Pathogens to Predict a Potential Novel Multi-Epitopes Vaccine Candidate
title Pan-Genome Analysis of Oral Bacterial Pathogens to Predict a Potential Novel Multi-Epitopes Vaccine Candidate
title_full Pan-Genome Analysis of Oral Bacterial Pathogens to Predict a Potential Novel Multi-Epitopes Vaccine Candidate
title_fullStr Pan-Genome Analysis of Oral Bacterial Pathogens to Predict a Potential Novel Multi-Epitopes Vaccine Candidate
title_full_unstemmed Pan-Genome Analysis of Oral Bacterial Pathogens to Predict a Potential Novel Multi-Epitopes Vaccine Candidate
title_short Pan-Genome Analysis of Oral Bacterial Pathogens to Predict a Potential Novel Multi-Epitopes Vaccine Candidate
title_sort pan-genome analysis of oral bacterial pathogens to predict a potential novel multi-epitopes vaccine candidate
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9320593/
https://www.ncbi.nlm.nih.gov/pubmed/35886259
http://dx.doi.org/10.3390/ijerph19148408
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