Evidence map›Paper›PMID 28081260›Full record

ArticlePloS one2017

Comparative Genome Sequencing Reveals Within-Host Genetic Changes in Neisseria meningitidis during Invasive Disease.

Johanna Klughammer, Marcus Dittrich, Jochen Blom, Vera Mitesser, Ulrich Vogel, Matthias Frosch, Alexander Goesmann, Tobias Müller, Christoph Schoen

Open access · goldAbstract readComparative Study
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

29 citing papers in PubMed, 33 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Investigation of invasiveFrontiers in public health · 2025
    Article
  5. Frontiers in cellular and infection microbiology · 2025
    Review
  6. Sweet complexity:Frontiers in cellular and infection microbiology · 2024
    Review
  7. Review
  8. Genomic analysis ofNew microbes and new infections · 2023
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Atypical, Yet Not Infrequent, Infections withPathogens (Basel, Switzerland) · 2019
    Review
  16. Article
  17. Article
  18. Article
  19. Genus-Wide Comparative Genomics Analysis ofInternational journal of genomics · 2019
    Article
  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

9 authors at 3 institutions in 2 countries.

Johanna KlughammerCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.
Marcus DittrichDepartment of Bioinformatics, Biocenter, University of Würzburg, Würzburg, Germany.
Jochen BlomInstitute for Bioinformatics and Systems Biology, Justus Liebig University Giessen, Giessen, Germany.
Vera MitesserInstitute for Hygiene and Microbiology, University of Würzburg, Würzburg, Germany.
Ulrich VogelInstitute for Hygiene and Microbiology, University of Würzburg, Würzburg, Germany.
Matthias FroschInstitute for Hygiene and Microbiology, University of Würzburg, Würzburg, Germany.
Alexander GoesmannInstitute for Bioinformatics and Systems Biology, Justus Liebig University Giessen, Giessen, Germany.
Tobias MüllerDepartment of Bioinformatics, Biocenter, University of Würzburg, Würzburg, Germany.
Christoph SchoenInstitute for Hygiene and Microbiology, University of Würzburg, Würzburg, Germany.ORCID http://orcid.org/0000-0003-2222-1085
University of Würzburg · DEJustus-Liebig-Universität Gießen · DEAustrian Academy of Sciences · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Some members of the physiological human microbiome occasionally cause life-threatening disease even in immunocompetent individuals. A prime example of such a commensal pathogen is Neisseria meningitidis, which normally resides in the human nasopharynx but is also a leading cause of sepsis and epidemic meningitis. Using N. meningitidis as model organism, we tested the hypothesis that virulence of commensal pathogens is a consequence of within host evolution and selection of invasive variants due to mutations at contingency genes, a mechanism called phase variation. In line with the hypothesis that phase variation evolved as an adaptation to colonize diverse hosts, computational comparisons of all 27 to date completely sequenced and annotated meningococcal genomes retrieved from public databases showed that contingency genes are indeed enriched for genes involved in host interactions. To assess within-host genetic changes in meningococci, we further used ultra-deep whole-genome sequencing of throat-blood strain pairs isolated from four patients suffering from invasive meningococcal disease. We detected up to three mutations per strain pair, affecting predominantly contingency genes involved in type IV pilus biogenesis. However, there was not a single (set) of mutation(s) that could invariably be found in all four pairs of strains. Phenotypic assays further showed that these genetic changes were generally not associated with increased serum resistance, higher fitness in human blood ex vivo or differences in the interaction with human epithelial and endothelial cells in vitro. In conclusion, we hypothesize that virulence of meningococci results from accidental emergence of invasive variants during carriage and without within host evolution of invasive phenotypes during disease progression in vivo.

Indexed as

Evolution, MolecularGenome, BacterialMutationNeisseria meningitidisCell LineFemaleHigh-Throughput Nucleotide SequencingHost-Pathogen InteractionsHumansMaleMeningococcal Infections

Identifiers

PMID28081260
PMCPMC5231331
OpenAlexW2579040461

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.