Cargando…

Pan-Genome Analysis of Human Gastric Pathogen H. pylori: Comparative Genomics and Pathogenomics Approaches to Identify Regions Associated with Pathogenicity and Prediction of Potential Core Therapeutic Targets

Helicobacter pylori is a human gastric pathogen implicated as the major cause of peptic ulcer and second leading cause of gastric cancer (~70%) around the world. Conversely, an increased resistance to antibiotics and hindrances in the development of vaccines against H. pylori are observed. Pan-genom...

Descripción completa

Detalles Bibliográficos
Autores principales: Ali, Amjad, Naz, Anam, Soares, Siomar C, Bakhtiar, Marriam, Tiwari, Sandeep, Hassan, Syed S, Hanan, Fazal, Ramos, Rommel, Pereira, Ulisses, Barh, Debmalya, Figueiredo, Henrique César Pereira, Ussery, David W., Miyoshi, Anderson, Silva, Artur, Azevedo, Vasco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4325212/
https://www.ncbi.nlm.nih.gov/pubmed/25705648
http://dx.doi.org/10.1155/2015/139580
_version_ 1782356784859578368
author Ali, Amjad
Naz, Anam
Soares, Siomar C
Bakhtiar, Marriam
Tiwari, Sandeep
Hassan, Syed S
Hanan, Fazal
Ramos, Rommel
Pereira, Ulisses
Barh, Debmalya
Figueiredo, Henrique César Pereira
Ussery, David W.
Miyoshi, Anderson
Silva, Artur
Azevedo, Vasco
author_facet Ali, Amjad
Naz, Anam
Soares, Siomar C
Bakhtiar, Marriam
Tiwari, Sandeep
Hassan, Syed S
Hanan, Fazal
Ramos, Rommel
Pereira, Ulisses
Barh, Debmalya
Figueiredo, Henrique César Pereira
Ussery, David W.
Miyoshi, Anderson
Silva, Artur
Azevedo, Vasco
author_sort Ali, Amjad
collection PubMed
description Helicobacter pylori is a human gastric pathogen implicated as the major cause of peptic ulcer and second leading cause of gastric cancer (~70%) around the world. Conversely, an increased resistance to antibiotics and hindrances in the development of vaccines against H. pylori are observed. Pan-genome analyses of the global representative H. pylori isolates consisting of 39 complete genomes are presented in this paper. Phylogenetic analyses have revealed close relationships among geographically diverse strains of H. pylori. The conservation among these genomes was further analyzed by pan-genome approach; the predicted conserved gene families (1,193) constitute ~77% of the average H. pylori genome and 45% of the global gene repertoire of the species. Reverse vaccinology strategies have been adopted to identify and narrow down the potential core-immunogenic candidates. Total of 28 nonhost homolog proteins were characterized as universal therapeutic targets against H. pylori based on their functional annotation and protein-protein interaction. Finally, pathogenomics and genome plasticity analysis revealed 3 highly conserved and 2 highly variable putative pathogenicity islands in all of the H. pylori genomes been analyzed.
format Online
Article
Text
id pubmed-4325212
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Hindawi Publishing Corporation
record_format MEDLINE/PubMed
spelling pubmed-43252122015-02-22 Pan-Genome Analysis of Human Gastric Pathogen H. pylori: Comparative Genomics and Pathogenomics Approaches to Identify Regions Associated with Pathogenicity and Prediction of Potential Core Therapeutic Targets Ali, Amjad Naz, Anam Soares, Siomar C Bakhtiar, Marriam Tiwari, Sandeep Hassan, Syed S Hanan, Fazal Ramos, Rommel Pereira, Ulisses Barh, Debmalya Figueiredo, Henrique César Pereira Ussery, David W. Miyoshi, Anderson Silva, Artur Azevedo, Vasco Biomed Res Int Research Article Helicobacter pylori is a human gastric pathogen implicated as the major cause of peptic ulcer and second leading cause of gastric cancer (~70%) around the world. Conversely, an increased resistance to antibiotics and hindrances in the development of vaccines against H. pylori are observed. Pan-genome analyses of the global representative H. pylori isolates consisting of 39 complete genomes are presented in this paper. Phylogenetic analyses have revealed close relationships among geographically diverse strains of H. pylori. The conservation among these genomes was further analyzed by pan-genome approach; the predicted conserved gene families (1,193) constitute ~77% of the average H. pylori genome and 45% of the global gene repertoire of the species. Reverse vaccinology strategies have been adopted to identify and narrow down the potential core-immunogenic candidates. Total of 28 nonhost homolog proteins were characterized as universal therapeutic targets against H. pylori based on their functional annotation and protein-protein interaction. Finally, pathogenomics and genome plasticity analysis revealed 3 highly conserved and 2 highly variable putative pathogenicity islands in all of the H. pylori genomes been analyzed. Hindawi Publishing Corporation 2015 2015-01-29 /pmc/articles/PMC4325212/ /pubmed/25705648 http://dx.doi.org/10.1155/2015/139580 Text en Copyright © 2015 Amjad Ali et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Ali, Amjad
Naz, Anam
Soares, Siomar C
Bakhtiar, Marriam
Tiwari, Sandeep
Hassan, Syed S
Hanan, Fazal
Ramos, Rommel
Pereira, Ulisses
Barh, Debmalya
Figueiredo, Henrique César Pereira
Ussery, David W.
Miyoshi, Anderson
Silva, Artur
Azevedo, Vasco
Pan-Genome Analysis of Human Gastric Pathogen H. pylori: Comparative Genomics and Pathogenomics Approaches to Identify Regions Associated with Pathogenicity and Prediction of Potential Core Therapeutic Targets
title Pan-Genome Analysis of Human Gastric Pathogen H. pylori: Comparative Genomics and Pathogenomics Approaches to Identify Regions Associated with Pathogenicity and Prediction of Potential Core Therapeutic Targets
title_full Pan-Genome Analysis of Human Gastric Pathogen H. pylori: Comparative Genomics and Pathogenomics Approaches to Identify Regions Associated with Pathogenicity and Prediction of Potential Core Therapeutic Targets
title_fullStr Pan-Genome Analysis of Human Gastric Pathogen H. pylori: Comparative Genomics and Pathogenomics Approaches to Identify Regions Associated with Pathogenicity and Prediction of Potential Core Therapeutic Targets
title_full_unstemmed Pan-Genome Analysis of Human Gastric Pathogen H. pylori: Comparative Genomics and Pathogenomics Approaches to Identify Regions Associated with Pathogenicity and Prediction of Potential Core Therapeutic Targets
title_short Pan-Genome Analysis of Human Gastric Pathogen H. pylori: Comparative Genomics and Pathogenomics Approaches to Identify Regions Associated with Pathogenicity and Prediction of Potential Core Therapeutic Targets
title_sort pan-genome analysis of human gastric pathogen h. pylori: comparative genomics and pathogenomics approaches to identify regions associated with pathogenicity and prediction of potential core therapeutic targets
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4325212/
https://www.ncbi.nlm.nih.gov/pubmed/25705648
http://dx.doi.org/10.1155/2015/139580
work_keys_str_mv AT aliamjad pangenomeanalysisofhumangastricpathogenhpyloricomparativegenomicsandpathogenomicsapproachestoidentifyregionsassociatedwithpathogenicityandpredictionofpotentialcoretherapeutictargets
AT nazanam pangenomeanalysisofhumangastricpathogenhpyloricomparativegenomicsandpathogenomicsapproachestoidentifyregionsassociatedwithpathogenicityandpredictionofpotentialcoretherapeutictargets
AT soaressiomarc pangenomeanalysisofhumangastricpathogenhpyloricomparativegenomicsandpathogenomicsapproachestoidentifyregionsassociatedwithpathogenicityandpredictionofpotentialcoretherapeutictargets
AT bakhtiarmarriam pangenomeanalysisofhumangastricpathogenhpyloricomparativegenomicsandpathogenomicsapproachestoidentifyregionsassociatedwithpathogenicityandpredictionofpotentialcoretherapeutictargets
AT tiwarisandeep pangenomeanalysisofhumangastricpathogenhpyloricomparativegenomicsandpathogenomicsapproachestoidentifyregionsassociatedwithpathogenicityandpredictionofpotentialcoretherapeutictargets
AT hassansyeds pangenomeanalysisofhumangastricpathogenhpyloricomparativegenomicsandpathogenomicsapproachestoidentifyregionsassociatedwithpathogenicityandpredictionofpotentialcoretherapeutictargets
AT hananfazal pangenomeanalysisofhumangastricpathogenhpyloricomparativegenomicsandpathogenomicsapproachestoidentifyregionsassociatedwithpathogenicityandpredictionofpotentialcoretherapeutictargets
AT ramosrommel pangenomeanalysisofhumangastricpathogenhpyloricomparativegenomicsandpathogenomicsapproachestoidentifyregionsassociatedwithpathogenicityandpredictionofpotentialcoretherapeutictargets
AT pereiraulisses pangenomeanalysisofhumangastricpathogenhpyloricomparativegenomicsandpathogenomicsapproachestoidentifyregionsassociatedwithpathogenicityandpredictionofpotentialcoretherapeutictargets
AT barhdebmalya pangenomeanalysisofhumangastricpathogenhpyloricomparativegenomicsandpathogenomicsapproachestoidentifyregionsassociatedwithpathogenicityandpredictionofpotentialcoretherapeutictargets
AT figueiredohenriquecesarpereira pangenomeanalysisofhumangastricpathogenhpyloricomparativegenomicsandpathogenomicsapproachestoidentifyregionsassociatedwithpathogenicityandpredictionofpotentialcoretherapeutictargets
AT usserydavidw pangenomeanalysisofhumangastricpathogenhpyloricomparativegenomicsandpathogenomicsapproachestoidentifyregionsassociatedwithpathogenicityandpredictionofpotentialcoretherapeutictargets
AT miyoshianderson pangenomeanalysisofhumangastricpathogenhpyloricomparativegenomicsandpathogenomicsapproachestoidentifyregionsassociatedwithpathogenicityandpredictionofpotentialcoretherapeutictargets
AT silvaartur pangenomeanalysisofhumangastricpathogenhpyloricomparativegenomicsandpathogenomicsapproachestoidentifyregionsassociatedwithpathogenicityandpredictionofpotentialcoretherapeutictargets
AT azevedovasco pangenomeanalysisofhumangastricpathogenhpyloricomparativegenomicsandpathogenomicsapproachestoidentifyregionsassociatedwithpathogenicityandpredictionofpotentialcoretherapeutictargets