Evidence map›Paper›PMID 27821148›Full record

ArticleBMC infectious diseases2016

Understanding pneumococcal serotype 1 biology through population genomic analysis.

Chrispin Chaguza, Jennifer E Cornick, Simon R Harris, Cheryl P Andam, Laura Bricio-Moreno, Marie Yang, Feyruz Yalcin, Sani Ousmane, Shanil Govindpersad, Madikay Senghore and 20 more

Open access · goldAbstract read
In one paragraph

Article in BMC infectious diseases, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
5.0field-weighted citation impact, top 4% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

  1. Molecular Epidemiology ofInternational journal of molecular sciences · 2025
    Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Genomic Characteristics of InvasiveBioinformatics and biology insights · 2020
    Article
  11. LastingJournal of oral microbiology · 2020
    Article
  12. Article
  13. Puzzling Over the Pneumococcal Pangenome.Frontiers in microbiology · 2018
    Review
  14. 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

30 authors at 14 institutions in 10 countries.

Chrispin ChaguzaDepartment of Clinical Infection, Microbiology and Immunology, Institute of Infection and Global Health, University of Liverpool, Liverpool, L69 7BE, UK. Chrispin.Chaguza@liverpool.ac.uk.ORCID 0000-0002-2108-1757
Jennifer E CornickDepartment of Clinical Infection, Microbiology and Immunology, Institute of Infection and Global Health, University of Liverpool, Liverpool, L69 7BE, UK.
Simon R HarrisPathogen Genomics, Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Cambridge, CB10 1SA, UK.
Cheryl P AndamDepartment of Clinical Infection, Microbiology and Immunology, Institute of Infection and Global Health, University of Liverpool, Liverpool, L69 7BE, UK.
Laura Bricio-MorenoDepartment of Clinical Infection, Microbiology and Immunology, Institute of Infection and Global Health, University of Liverpool, Liverpool, L69 7BE, UK.
Marie YangDepartment of Clinical Infection, Microbiology and Immunology, Institute of Infection and Global Health, University of Liverpool, Liverpool, L69 7BE, UK.
Feyruz YalcinPathogen Genomics, Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Cambridge, CB10 1SA, UK.
Sani OusmaneUnité de Biologie, Centre de Recherche Médicale et Sanitaire (CERMES), Niamey, Niger.
Shanil GovindpersadNational Institute for Communicable Diseases (NICD), Johannesburg, South Africa.
Madikay SenghoreBacterial Diseases Programme, Medical Research Council (MRC), Banjul, The Gambia.
Chinelo EbrukeBacterial Diseases Programme, Medical Research Council (MRC), Banjul, The Gambia.
Mignon Du PlessisNational Institute for Communicable Diseases (NICD), Johannesburg, South Africa.
Anmol M KiranDepartment of Clinical Infection, Microbiology and Immunology, Institute of Infection and Global Health, University of Liverpool, Liverpool, L69 7BE, UK.
Gerd PluschkeSwiss Tropical and Public Health Institute, Basel, Switzerland.
Betuel SigauqueCentro de Investigação em Saúde da Manhiça, Maputo, Mozambique.
Lesley McGeeRespiratory Diseases Branch, Centers for Disease Control and Prevention, Atlanta, Georgia, GA 30329, USA.
Keith P KlugmanHubert Department of Global Health, Rollins School of Public Health, Emory University, Atlanta, GA, 30322, USA.
Paul TurnerCambodia Oxford Medical Research Unit, Angkor Hospital for Children, Siem Reap, Cambodia.
Jukka CoranderDepartment of Mathematics and Statistics, University of Helsinki, Helsinki, Finland.
Julian ParkhillPathogen Genomics, Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Cambridge, CB10 1SA, UK.
Jean-Marc CollardUnité de Biologie, Centre de Recherche Médicale et Sanitaire (CERMES), Niamey, Niger.
Martin AntonioBacterial Diseases Programme, Medical Research Council (MRC), Banjul, The Gambia.
Anne von GottbergNational Institute for Communicable Diseases (NICD), Johannesburg, South Africa.
Robert S HeydermanMalawi-Liverpool-Wellcome Trust Clinical Research Programme, Queen Elizabeth Central Hospital, Blantyre, Malawi.
Neil FrenchDepartment of Clinical Infection, Microbiology and Immunology, Institute of Infection and Global Health, University of Liverpool, Liverpool, L69 7BE, UK.
Aras KadiogluDepartment of Clinical Infection, Microbiology and Immunology, Institute of Infection and Global Health, University of Liverpool, Liverpool, L69 7BE, UK.
William P HanageDepartment of Epidemiology, Center for Communicable Disease Dynamics, Harvard T. H. Chan School of Public Health, Massachusetts, MA, 02115, USA.
Dean B EverettDepartment of Clinical Infection, Microbiology and Immunology, Institute of Infection and Global Health, University of Liverpool, Liverpool, L69 7BE, UK.
Stephen D BentleyDepartment of Clinical Infection, Microbiology and Immunology, Institute of Infection and Global Health, University of Liverpool, Liverpool, L69 7BE, UK. sdb@sanger.ac.uk.
PAGe Consortium
University of Liverpool · GBWellcome Sanger Institute · GBCenter for Disease Dynamics, Economics & Policy · USCentre de Recherche Médicale et Sanitaire · NENational Institute for Communicable DiseasesUniversity of London · GBAngkor Hospital for Children · KHCenters for Disease Control and Prevention · USGates Foundation · USManhiça Health Research Centre · MZStatistics Finland · FISwiss Tropical and Public Health Institute · CHUniversity of the Witwatersrand · ZAUniversity of Warwick · 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
Medical Research Council MC_U190074190Medical Research Council MC_U190081991Medical Research Council MC_UP_A900_1122NIAID NIH HHS R01 AI106786Wellcome Trust 084679/Z/08/ZWellcome Trust 100891
6 · The paper itself

Abstract

backgroundPneumococcus kills over one million children annually and over 90 % of these deaths occur in low-income countries especially in Sub-Saharan Africa (SSA) where HIV exacerbates the disease burden. In SSA, serotype 1 pneumococci particularly the endemic ST217 clone, causes majority of the pneumococcal disease burden. To understand the evolution of the virulent ST217 clone, we analysed ST217 whole genomes from isolates sampled from African and Asian countries.

methodsWe analysed 226 whole genome sequences from the ST217 lineage sampled from 9 African and 4 Asian countries. We constructed a whole genome alignment and used it for phylogenetic and coalescent analyses. We also screened the genomes to determine presence of antibiotic resistance conferring genes.

resultsPopulation structure analysis grouped the ST217 isolates into five sequence clusters (SCs), which were highly associated with different geographical regions and showed limited intracontinental and intercontinental spread. The SCs showed lower than expected genomic sequence, which suggested strong purifying selection and small population sizes caused by bottlenecks. Recombination rates varied between the SCs but were lower than in other successful clones such as PMEN1. African isolates showed higher prevalence of antibiotic resistance genes than Asian isolates. Interestingly, certain West African isolates harbored a defective chloramphenicol and tetracycline resistance-conferring element (Tn5253) with a deletion in the loci encoding the chloramphenicol resistance gene (cat

conclusionsThe high phylogeographic diversity of the ST217 clone shows that this clone has been in circulation globally for a long time, which allowed its diversification and adaptation in different geographical regions. Such geographic adaptation reflects local variations in selection pressures in different locales. Further studies will be required to fully understand the biological mechanisms which makes the ST217 clone highly invasive but unable to successfully colonise the human nasopharynx for long durations which results in lower recombination rates.

Indexed as

AfricaAsiaDrug Resistance, BacterialGenetic VariationHumansNasopharynxPhylogenyPneumococcal InfectionsRecombination, GeneticSelection, GeneticSerogroupStreptococcus pneumoniaeTetracycline ResistanceAntibiotic resistanceEvolutionPhylogeographyPneumococcal serotype 1ST217

Identifiers

PMID27821148
PMCPMC5100261
OpenAlexW2553354970

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.