Evidence map›Paper›PMID 37129481›Full record

ArticleMicrobiology spectrum2023

Helicobacter pylori Modulates Heptose Metabolite Biosynthesis and Heptose-Dependent Innate Immune Host Cell Activation by Multiple Mechanisms.

Martina Hauke, Felix Metz, Johanna Rapp, Larissa Faass, Simon H Bats, Sandra Radziej, Hannes Link, Wolfgang Eisenreich, Christine Josenhans

Open access · goldAbstract read
In one paragraph

Article in Microbiology spectrum, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Managing dangerous liaisons: lessons fromJournal of bacteriology · 2026
    Review
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  4. Review
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  6. Article
  7. Trained Immunity and Trained Tolerance: The Case ofInternational journal of molecular sciences · 2024
    Review
  8. Research progress on molecular mechanism of pyroptosis caused byAnnals of medicine and surgery (2012) · 2024
    Review
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

9 authors at 2 institutions in 1 country.

Martina HaukeMax von Pettenkofer Institute, Ludwig Maximilians University Munich, München, Germany.
Felix MetzMax von Pettenkofer Institute, Ludwig Maximilians University Munich, München, Germany.
Johanna RappBacterial Metabolomics, CMFI, University Tübingen, Tübingen, Germany.
Larissa FaassMax von Pettenkofer Institute, Ludwig Maximilians University Munich, München, Germany.
Simon H BatsMax von Pettenkofer Institute, Ludwig Maximilians University Munich, München, Germany.
Sandra RadziejBavarian NMR Center-Structural Membrane Biochemistry, Department of Chemistry, Technical University Munich, Garching, Germany.
Hannes LinkBacterial Metabolomics, CMFI, University Tübingen, Tübingen, Germany.
Wolfgang EisenreichBavarian NMR Center-Structural Membrane Biochemistry, Department of Chemistry, Technical University Munich, Garching, Germany.
Christine JosenhansMax von Pettenkofer Institute, Ludwig Maximilians University Munich, München, Germany.ORCID 0000-0003-4620-2954
Ludwig-Maximilians-Universität München · DEUniversity of Tübingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Heptose metabolites including ADP-d-glycero-β-d-manno-heptose (ADP-heptose) are involved in bacterial lipopolysaccharide and cell envelope biosynthesis. Recently, heptoses were also identified to have potent proinflammatory activity on human cells as novel microbe-associated molecular patterns. The gastric pathogenic bacterium Helicobacter pylori produces heptose metabolites, which it transports into human cells through its Cag type 4 secretion system. Using H. pylori as a model, we have addressed the question of how proinflammatory ADP-heptose biosynthesis can be regulated by bacteria. We have characterized the interstrain variability and regulation of heptose biosynthesis genes and the modulation of heptose metabolite production by H. pylori, which impact cell-autonomous proinflammatory human cell activation. HldE, a central enzyme of heptose metabolite biosynthesis, showed strong sequence variability between strains and was also variably expressed between strains. Amounts of gene transcripts in the

Indexed as

Helicobacter pyloriBacterial ProteinsHeptosesHumansImmunity, InnateInflammationLipopolysaccharidesBacterial ProteinsHeptosesLipopolysaccharidesADP-heptoseALPK1-TIFAbacterial metabolitesHelicobacter pyloriheptose-monophosphateinnate immunitylipopolysaccharidemass spectrometryNMR

Identifiers

PMID37129481
PMCPMC10269868
OpenAlexW4367323211

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.