Evidence map›Paper›PMID 25480686›Full record

ArticleGenome biology and evolution2014

Global phylogenomic analysis of nonencapsulated Streptococcus pneumoniae reveals a deep-branching classic lineage that is distinct from multiple sporadic lineages.

Markus Hilty, Daniel Wüthrich, Susannah J Salter, Hansjürg Engel, Samuel Campbell, Raquel Sá-Leão, Hermínia de Lencastre, Peter Hermans, Ewa Sadowy, Paul Turner and 18 more

Open access · goldAbstract read
In one paragraph

Article in Genome biology and evolution, 2014. 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
3.6field-weighted citation impact, top 7% 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

43 citing papers in PubMed, 53 citations in OpenAlex.

  1. AliC and AliD of nonencapsulatedFrontiers in cellular and infection microbiology · 2025
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  11. Identification of Streptococcus pneumoniae and other Mitis streptococci: importance of molecular methods.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2020
    Review
  12. Article
  13. Relationships among streptococci from the mitis group, misidentified as Streptococcus pneumoniae.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2020
    Article
  14. Comparative Analysis ofPathogens (Basel, Switzerland) · 2020
    Article
  15. Article
  16. The Best of All Worlds:Microorganisms · 2019
    Review
  17. Carbon source regulates polysaccharide capsule biosynthesis inThe Journal of biological chemistry · 2019
    Article
  18. 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

28 authors at 17 institutions in 10 countries.

Markus HiltyInstitute for Infectious Diseases, University of Bern, Switzerland Department of Infectious Diseases, Inselspital, Bern University Hospital and University of Bern, Switzerland markus.hilty@ifik.unibe.ch.
Daniel WüthrichInterfaculty Bioinformatics Unit, University of Bern, Switzerland Swiss Institute of Bioinformatics, Lausanne, Switzerland.
Susannah J SalterWellcome Trust Sanger Institute, Hinxton, United Kingdom.
Hansjürg EngelInstitute for Infectious Diseases, University of Bern, Switzerland.
Samuel CampbellInstitute for Infectious Diseases, University of Bern, Switzerland.
Raquel Sá-LeãoInstituto de Tecnologia Química e Biológica, University of Lisbon, Portugal.
Hermínia de LencastreInstituto de Tecnologia Química e Biológica, University of Lisbon, Portugal Laboratory of Microbiology and Infectious Diseases, The Rockefeller University.
Peter HermansLaboratory of Pediatric Infectious Diseases, Radboud University Medical Centre, Nijmegen, The Netherlands.
Ewa SadowyNational Medicines Institute, Warsaw, Poland.
Paul TurnerShoklo Malaria Research Unit, Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Mae Sot, Thailand Centre for Tropical Medicine, Nuffield Department of Medicine, University of Oxford, United Kingdom.
Claire ChewapreechaWellcome Trust Sanger Institute, Hinxton, United Kingdom Shoklo Malaria Research Unit, Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Mae Sot, Thailand.
Mathew DiggleClinical Microbiology Department, Queens Medical Centre, Nottingham, United Kingdom.
Gerd PluschkeSwiss Tropical and Public Health Institute, University of Basel, Switzerland.
Lesley McGeeRespiratory Diseases Branch, Centers for Disease Control and Prevention, Georgia, Atlanta.
Özgen Köseoğlu EserDepartment of Microbiology, Medical Faculty, Hacettepe University, Ankara, Turkey.
Donald E LowMt Sinai Hospital & Public Health Laboratories, Toronto, Ontario, Canada.
Heidi Smith-VaughanMenzies School of Health Research, Charles Darwin University, Australia.
Andrea EndimianiInstitute for Infectious Diseases, University of Bern, Switzerland.
Marianne KüfferInstitute for Infectious Diseases, University of Bern, Switzerland.
Mélanie DupasquierCentre for Integrative Genomics, University of Lausanne, Switzerland.
Emmanuel BeaudoingCentre for Integrative Genomics, University of Lausanne, Switzerland.
Johann WeberCentre for Integrative Genomics, University of Lausanne, Switzerland.
Rémy BruggmannInterfaculty Bioinformatics Unit, University of Bern, Switzerland Swiss Institute of Bioinformatics, Lausanne, Switzerland.
William P HanageDepartment of Epidemiology, Center for Communicable Disease Dynamics, Harvard School of Public Health.
Julian ParkhillWellcome Trust Sanger Institute, Hinxton, United Kingdom.
Lucy J HathawayInstitute for Infectious Diseases, University of Bern, Switzerland.
Kathrin MühlemannInstitute for Infectious Diseases, University of Bern, Switzerland Department of Infectious Diseases, Inselspital, Bern University Hospital and University of Bern, Switzerland.
Stephen D BentleyWellcome Trust Sanger Institute, Hinxton, United Kingdom Department of Medicine, Addenbrookes Hospital, University of Cambridge, United Kingdom.
University of Bern · CHWellcome Sanger Institute · GBUniversity of Lausanne · CHUniversity Hospital of Bern · CHCenter for Disease Dynamics, Economics & Policy · USCenters for Disease Control and Prevention · USHacettepe University · TRInstituto de Biologia Experimental e Tecnológica · PTMenzies School of Health Research · AUMount Sinai Hospital · CANarodowy Instytut Leków · PLQueen's Medical Centre · GBRadboud University Nijmegen · NLRockefeller University · USSIB Swiss Institute of Bioinformatics · CHSwiss Tropical and Public Health Institute · CHUniversity of Oxford · GB

Funding

Ecological and genetic contributions to the spread of resistance in pneumococcusR01AI106786 · NIAID · HARVARD SCHOOL OF PUBLIC HEALTH · PI HANAGE, WILLIAM · 2013 to 2017
$3.1M
NIAID NIH HHS R01 AI106786NIAID NIH HHS R01 AI106786-01Wellcome TrustWellcome Trust 083735/Z/07
6 · The paper itself

Abstract

The surrounding capsule of Streptococcus pneumoniae has been identified as a major virulence factor and is targeted by pneumococcal conjugate vaccines (PCV). However, nonencapsulated S. pneumoniae (non-Ec-Sp) have also been isolated globally, mainly in carriage studies. It is unknown if non-Ec-Sp evolve sporadically, if they have high antibiotic nonsusceptiblity rates and a unique, specific gene content. Here, whole-genome sequencing of 131 non-Ec-Sp isolates sourced from 17 different locations around the world was performed. Results revealed a deep-branching classic lineage that is distinct from multiple sporadic lineages. The sporadic lineages clustered with a previously sequenced, global collection of encapsulated S. pneumoniae (Ec-Sp) isolates while the classic lineage is comprised mainly of the frequently identified multilocus sequences types (STs) ST344 (n = 39) and ST448 (n = 40). All ST344 and nine ST448 isolates had high nonsusceptiblity rates to β-lactams and other antimicrobials. Analysis of the accessory genome reveals that the classic non-Ec-Sp contained an increased number of mobile elements, than Ec-Sp and sporadic non-Ec-Sp. Performing adherence assays to human epithelial cells for selected classic and sporadic non-Ec-Sp revealed that the presence of a integrative conjugative element (ICE) results in increased adherence to human epithelial cells (P = 0.005). In contrast, sporadic non-Ec-Sp lacking the ICE had greater growth in vitro possibly resulting in improved fitness. In conclusion, non-Ec-Sp isolates from the classic lineage have evolved separately. They have spread globally, are well adapted to nasopharyngeal carriage and are able to coexist with Ec-Sp. Due to continued use of PCV, non-Ec-Sp may become more prevalent.

Indexed as

Genome, BacterialPhylogenyAnti-Bacterial AgentsBacterial Capsulesbeta-LactamsCell LineDNA Transposable ElementsEpithelial CellsGenetic LociGenetic SpeciationHumansStreptococcus pneumoniaeAnti-Bacterial Agentsbeta-LactamsDNA Transposable Elementsantibiotic nonsusceptibilitycomparative genomicsintegrative conjugative elementspneumococcal isolateswhole-genome sequencing

Identifiers

PMID25480686
PMCPMC4986459
OpenAlexW2134752242

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.