Evidence map›Paper›PMID 32651390›Full record

ArticleNature communications2020

Within-host microevolution of Streptococcus pneumoniae is rapid and adaptive during natural colonisation.

Chrispin Chaguza, Madikay Senghore, Ebrima Bojang, Rebecca A Gladstone, Stephanie W Lo, Peggy-Estelle Tientcheu, Rowan E Bancroft, Archibald Worwui, Ebenezer Foster-Nyarko, Fatima Ceesay and 9 more

Abstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing 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

43 citing papers in PubMed.

  1. Review
  2. Article
  3. Low-Abundance and FragmentaryBiomolecules · 2026
    Article
  4. Article
  5. Emergence of multidrug-resistant ST876 serotype 14Frontiers in cellular and infection microbiology · 2026
    Article
  6. Genetic diversity ofGut microbes · 2025
    Article
  7. Article
  8. Article
  9. Review
  10. Population sequencing for phylogenetic diversity and transmission analyses.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  11. Colonization dynamics ofInfection and immunity · 2025
    Article
  12. Phenotypic and genetic heterogeneity ofMicrobial genomics · 2025
    Article
  13. Article
  14. Ultrastructural, metabolic and genetic characteristics of determinants facilitating the acquisition of macrolide resistance by Streptococcus pneumoniae.Drug resistance updates : reviews and commentaries in antimicrobial and anticancer chemotherapy · 2024
    Article
  15. Article
  16. Article
  17. Biological puzzles solved by usingJournal of bacteriology · 2024
    Review
  18. Estimating geographical spread ofMicrobial genomics · 2024
    Article
  19. 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

19 authors.

Chrispin Chaguza *Parasites and Microbes Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK. cc19@sanger.ac.uk.ORCID http://orcid.org/0000-0002-2108-1757
Madikay Senghore *Medical Research Council (MRC) Unit The Gambia at the London School of Hygiene and Tropical Medicine, Fajara, The Gambia.
Ebrima BojangMedical Research Council (MRC) Unit The Gambia at the London School of Hygiene and Tropical Medicine, Fajara, The Gambia.
Rebecca A GladstoneParasites and Microbes Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK.
Stephanie W LoParasites and Microbes Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK.
Peggy-Estelle TientcheuMedical Research Council (MRC) Unit The Gambia at the London School of Hygiene and Tropical Medicine, Fajara, The Gambia.ORCID http://orcid.org/0000-0002-4658-5628
Rowan E BancroftMedical Research Council (MRC) Unit The Gambia at the London School of Hygiene and Tropical Medicine, Fajara, The Gambia.
Archibald WorwuiMedical Research Council (MRC) Unit The Gambia at the London School of Hygiene and Tropical Medicine, Fajara, The Gambia.
Ebenezer Foster-NyarkoMedical Research Council (MRC) Unit The Gambia at the London School of Hygiene and Tropical Medicine, Fajara, The Gambia.
Fatima CeesayMedical Research Council (MRC) Unit The Gambia at the London School of Hygiene and Tropical Medicine, Fajara, The Gambia.
Catherine OkoiMedical Research Council (MRC) Unit The Gambia at the London School of Hygiene and Tropical Medicine, Fajara, The Gambia.
Lesley McGeeRespiratory Diseases Branch, Centers for Disease Control and Prevention, Atlanta, USA.
Keith P KlugmanHubert Department of Global Health, Rollins School of Public Health, Emory University, Atlanta, USA.
Robert F BreimanEmory Global Health Institute, Emory University, Atlanta, USA.
Michael R BarerDepartment of Infection, Immunity and Inflammation, University of Leicester, Leicester, UK.
Richard A AdegbolaRAMBICON Immunisation & Global Health Consulting, 6A Platinum Close, Lekki, Lagos State, Nigeria.
Martin AntonioMedical Research Council (MRC) Unit The Gambia at the London School of Hygiene and Tropical Medicine, Fajara, The Gambia.
Stephen D BentleyParasites and Microbes Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK. sdb@sanger.ac.uk.ORCID http://orcid.org/0000-0001-8094-3751
Brenda A Kwambana-AdamsMedical Research Council (MRC) Unit The Gambia at the London School of Hygiene and Tropical Medicine, Fajara, The Gambia. brenda.kwambana@ucl.ac.uk.ORCID http://orcid.org/0000-0002-1202-8540

Funding

Medical Research Council MR/R003076/1
6 · The paper itself

Abstract

Genomic evolution, transmission and pathogenesis of Streptococcus pneumoniae, an opportunistic human-adapted pathogen, is driven principally by nasopharyngeal carriage. However, little is known about genomic changes during natural colonisation. Here, we use whole-genome sequencing to investigate within-host microevolution of naturally carried pneumococci in ninety-eight infants intensively sampled sequentially from birth until twelve months in a high-carriage African setting. We show that neutral evolution and nucleotide substitution rates up to forty-fold faster than observed over longer timescales in S. pneumoniae and other bacteria drives high within-host pneumococcal genetic diversity. Highly divergent co-existing strain variants emerge during colonisation episodes through real-time intra-host homologous recombination while the rest are co-transmitted or acquired independently during multiple colonisation episodes. Genic and intergenic parallel evolution occur particularly in antibiotic resistance, immune evasion and epithelial adhesion genes. Our findings suggest that within-host microevolution is rapid and adaptive during natural colonisation.

Indexed as

Evolution, MolecularGeneticsGenome, BacterialHumansPneumococcal InfectionsStreptococcus pneumoniaeWhole Genome Sequencing

Identifiers

PMID32651390
PMCPMC7351774

What OpenQuestion holds

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Registered trials

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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.