Evidence map›Paper›PMID 25705648›Full record

ArticleBioMed research international2015

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.

Amjad Ali, Anam Naz, Siomar C Soares, Marriam Bakhtiar, Sandeep Tiwari, Syed S Hassan, Fazal Hanan, Rommel Ramos, Ulisses Pereira, Debmalya Barh and 5 more

Abstract read
In one paragraph

Article in BioMed research international, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

28 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. TargetingMolecules (Basel, Switzerland) · 2023
    Article
  6. Review
  7. Novel Chimeric Vaccine Candidate Development againstInternational journal of environmental research and public health · 2022
    Article
  8. Article
  9. Computer-Aided Multi-Epitope Vaccine Design againstInternational journal of environmental research and public health · 2022
    Article
  10. Vaccinomics to Design a Multi-Epitopes Vaccine forInternational journal of environmental research and public health · 2022
    Article
  11. Article
  12. Article
  13. Towards A Novel Multi-Epitopes Chimeric Vaccine for Simulating Strong Immune Responses and Protection againstInternational journal of environmental research and public health · 2021
    Article
  14. Article
  15. Whole-Genome Sequencing and Comparative Genomics of ThreePathogens (Basel, Switzerland) · 2021
    Article
  16. Article
  17. Article
  18. Review
  19. Pan-genomics in the human genome era.Nature reviews. Genetics · 2020
    Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Amjad AliAtta-ur-Rahman School of Applied Biosciences (ASAB), National University of Sciences and Technology (NUST), Islamabad 44000, Pakistan ; Laboratory of Cellular and Molecular Genetics, Federal University of Minas Gerais (UFMG), 31907-270 Belo Horizonte, MG, Brazil.
Anam NazAtta-ur-Rahman School of Applied Biosciences (ASAB), National University of Sciences and Technology (NUST), Islamabad 44000, Pakistan.
Siomar C SoaresLaboratory of Cellular and Molecular Genetics, Federal University of Minas Gerais (UFMG), 31907-270 Belo Horizonte, MG, Brazil.
Marriam BakhtiarLaboratory of Cellular and Molecular Genetics, Federal University of Minas Gerais (UFMG), 31907-270 Belo Horizonte, MG, Brazil ; Department of Bioinformatics, Mohammad Ali Jinnah University (MAJU), Sehala Road, Islamabad 44000, Pakistan.
Sandeep TiwariLaboratory of Cellular and Molecular Genetics, Federal University of Minas Gerais (UFMG), 31907-270 Belo Horizonte, MG, Brazil.
Syed S HassanLaboratory of Cellular and Molecular Genetics, Federal University of Minas Gerais (UFMG), 31907-270 Belo Horizonte, MG, Brazil.
Fazal HananKIMS, Khyber Medical University, Peshawar 25000, Pakistan.
Rommel RamosFederal University of Pará, 66075-110 Belém, PA, Brazil.
Ulisses PereiraLaboratory of Cellular and Molecular Genetics, Federal University of Minas Gerais (UFMG), 31907-270 Belo Horizonte, MG, Brazil ; Laboratory of Aquatic Animal Diseases (AQUAVET), Department of Preventive Veterinary Medicine, Federal University of Minas Gerais, 31907-270 Belo Horizonte, MG, Brazil.
Debmalya BarhCentre for Genomics and Applied Gene Technology, Institute of Integrative Omics and Applied Biotechnology (IIOAB), Nonakuri, Purba Medinipur, West Bengal 721172, India.
Henrique César Pereira FigueiredoLaboratory of Aquatic Animal Diseases (AQUAVET), Department of Preventive Veterinary Medicine, Federal University of Minas Gerais, 31907-270 Belo Horizonte, MG, Brazil.
David W UsseryCentre for Biological Sequence Analysis (CBS), Technical University of Denmark, 2800 Kongens Lyngby, Denmark.
Anderson MiyoshiLaboratory of Cellular and Molecular Genetics, Federal University of Minas Gerais (UFMG), 31907-270 Belo Horizonte, MG, Brazil.
Artur SilvaFederal University of Pará, 66075-110 Belém, PA, Brazil.
Vasco AzevedoLaboratory of Cellular and Molecular Genetics, Federal University of Minas Gerais (UFMG), 31907-270 Belo Horizonte, MG, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

DNA, BacterialGenetic VariationGenome, BacterialGenomic IslandsGenomicsHelicobacter InfectionsHelicobacter pyloriHumansPhylogenyStomachStomach NeoplasmsVirulenceDNA, Bacterial

Identifiers

PMID25705648
PMCPMC4325212

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.