Evidence map›Paper›PMID 20537153›Full record

ArticleBMC genomics2010

From array-based hybridization of Helicobacter pylori isolates to the complete genome sequence of an isolate associated with MALT lymphoma.

Jean-Michel Thiberge, Caroline Boursaux-Eude, Philippe Lehours, Marie-Agnès Dillies, Sophie Creno, Jean-Yves Coppée, Zoé Rouy, Aurélie Lajus, Laurence Ma, Christophe Burucoa and 11 more

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
8.9field-weighted citation impact, top 2% of its field
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

34 citing papers in PubMed, 57 citations in OpenAlex.

  1. Resistome and virulome determination inMicrobiology spectrum · 2025
    Article
  2. Characterization and Genomic Analysis of a New Phage InfectingInternational journal of molecular sciences · 2022
    Article
  3. Article
  4. Pathogenicity of Helicobacter pylori in cancer development and impacts of vaccination.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2019
    Review
  5. Relating Phage Genomes toInternational journal of molecular sciences · 2018
    Review
  6. A SystematicCurrent genomics · 2017
    Article
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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

21 authors at 6 institutions in 1 country.

Jean-Michel ThibergeInstitut Pasteur, Unité postulante de Pathogenèse de Helicobacter, Paris, France.
Caroline Boursaux-Eude
Philippe Lehours
Marie-Agnès Dillies
Sophie Creno
Jean-Yves Coppée
Zoé Rouy
Aurélie Lajus
Laurence Ma
Christophe Burucoa
Anne Ruskoné-Foumestraux
Anne Courillon-Mallet
Hilde De Reuse
Ivo Gomperts Boneca
Dominique Lamarque
Francis Mégraud
Jean-Charles Delchier
Claudine Médigue
Christiane Bouchier
Agnès Labigne
Josette Raymond
Institut Pasteur · FRCentre National de la Recherche Scientifique · FRInserm · FRDélégation Paris 5 · FRHôtel-Dieu de Paris · FRSorbonne Université · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHelicobacter pylori infection is associated with several gastro-duodenal inflammatory diseases of various levels of severity. To determine whether certain combinations of genetic markers can be used to predict the clinical source of the infection, we analyzed well documented and geographically homogenous clinical isolates using a comparative genomics approach.

resultsA set of 254 H. pylori genes was used to perform array-based comparative genomic hybridization among 120 French H. pylori strains associated with chronic gastritis (n = 33), duodenal ulcers (n = 27), intestinal metaplasia (n = 17) or gastric extra-nodal marginal zone B-cell MALT lymphoma (n = 43). Hierarchical cluster analyses of the DNA hybridization values allowed us to identify a homogeneous subpopulation of strains that clustered exclusively with cagPAI minus MALT lymphoma isolates. The genome sequence of B38, a representative of this MALT lymphoma strain-cluster, was completed, fully annotated, and compared with the six previously released H. pylori genomes (i.e. J99, 26695, HPAG1, P12, G27 and Shi470). B38 has the smallest H. pylori genome described thus far (1,576,758 base pairs containing 1,528 CDSs); it contains the vacAs2m2 allele and lacks the genes encoding the major virulence factors (absence of cagPAI, babB, babC, sabB, and homB). Comparative genomics led to the identification of very few sequences that are unique to the B38 strain (9 intact CDSs and 7 pseudogenes). Pair-wise genomic synteny comparisons between B38 and the 6 H. pylori sequenced genomes revealed an almost complete co-linearity, never seen before between the genomes of strain Shi470 (a Peruvian isolate) and B38.

conclusionThese isolates are deprived of the main H. pylori virulence factors characterized previously, but are nonetheless associated with gastric neoplasia.

Indexed as

Bacterial ProteinsCluster AnalysisDuodenal UlcerEvolution, MolecularGastritisGene Expression ProfilingGenome, BacterialGenomic IslandsHelicobacter pyloriHumansIntestinal DiseasesLymphoma, B-Cell, Marginal ZoneNucleic Acid HybridizationOligonucleotide Array Sequence AnalysisPhylogenySpecies SpecificityBacterial Proteins

Identifiers

PMID20537153
PMCPMC3091627
OpenAlexW1991671534

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.