Evidence map›Paper›PMID 30858837›Full record

ArticleFrontiers in microbiology2019

Genomic Analyses of >3,100 Nasopharyngeal Pneumococci Revealed Significant Differences Between Pneumococci Recovered in Four Different Geographical Regions.

Andries J van Tonder, James E Bray, Keith A Jolley, Melissa Jansen van Rensburg, Sigríður J Quirk, Gunnsteinn Haraldsson, Martin C J Maiden, Stephen D Bentley, Ásgeir Haraldsson, Helga Erlendsdóttir and 2 more

Abstract read
In one paragraph

Article in Frontiers in microbiology, 2019. 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
–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

8 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Biological puzzles solved by usingJournal of bacteriology · 2024
    Review
  5. Article
  6. Article
  7. Frontiers in cellular and infection microbiology · 2021
    Article
  8. 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

12 authors.

Andries J van TonderNuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.
James E BrayDepartment of Zoology, University of Oxford, Oxford, United Kingdom.
Keith A JolleyDepartment of Zoology, University of Oxford, Oxford, United Kingdom.
Melissa Jansen van RensburgDepartment of Medicine, Imperial College London, London, United Kingdom.
Sigríður J QuirkClinical Microbiology, University of Iceland and Landspitali University Hospital, Reykjavik, Iceland.
Gunnsteinn HaraldssonClinical Microbiology, University of Iceland and Landspitali University Hospital, Reykjavik, Iceland.
Martin C J MaidenDepartment of Zoology, University of Oxford, Oxford, United Kingdom.
Stephen D BentleyParasites and Microbes, Wellcome Sanger Institute, Hinxton, United Kingdom.
Ásgeir HaraldssonChildren's Hospital Iceland, Landspitali University Hospital, Reykjavik, Iceland.
Helga ErlendsdóttirClinical Microbiology, University of Iceland and Landspitali University Hospital, Reykjavik, Iceland.
Karl G KristinssonClinical Microbiology, University of Iceland and Landspitali University Hospital, Reykjavik, Iceland.
Angela B BrueggemannNuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.

Funding

Wellcome Trust 098051
6 · The paper itself

Abstract

Understanding the structure of a bacterial population is essential in order to understand bacterial evolution. Estimating the core genome (those genes common to all, or nearly all, strains of a species) is a key component of such analyses. The size and composition of the core genome varies by dataset, but we hypothesized that the variation between different collections of the same bacterial species would be minimal. To investigate this, we analyzed the genome sequences of 3,118 pneumococci recovered from healthy individuals in Reykjavik (Iceland), Southampton (United Kingdom), Boston (United States), and Maela (Thailand). The analyses revealed a "supercore" genome (genes shared by all 3,118 pneumococci) of 558 genes, although an additional 354 core genes were shared by pneumococci from Reykjavik, Southampton, and Boston. Overall, the size and composition of the core and pan-genomes among pneumococci recovered in Reykjavik, Southampton, and Boston were similar. Maela pneumococci were distinctly different in that they had a smaller core genome and larger pan-genome. The pan-genome of Maela pneumococci contained several >25 Kb sequence regions (flanked by pneumococcal genes) that were homologous to genomic regions found in other bacterial species. Overall, our work revealed that some subsets of the global pneumococcal population are highly heterogeneous, and our hypothesis was rejected. This is an important finding in terms of understanding genetic variation among pneumococci and is also an essential point of consideration before generalizing the findings from a single dataset to the wider pneumococcal population.

Indexed as

accessory genomebacterial population structurecore genomenext generation sequencingpan-genomepneumococcus

Identifiers

PMID30858837
PMCPMC6398412

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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.