Evidence map›Paper›PMID 35985351›Full record

ArticleThe Lancet. Microbe2022

Emergence of a multidrug-resistant and virulent Streptococcus pneumoniae lineage mediates serotype replacement after PCV13: an international whole-genome sequencing study.

Stephanie W Lo, Kate Mellor, Robert Cohen, Alba Redin Alonso, Sophie Belman, Narender Kumar, Paulina A Hawkins, Rebecca A Gladstone, Anne von Gottberg, Balaji Veeraraghavan and 30 more

Abstract read
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Article in The Lancet. Microbe, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 1 pooled it
–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

59 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Antimicrobial resistance ofFrontiers in public health · 2024
    Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Genomic epidemiology ofMicrobial genomics · 2026
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Serotype distribution and antimicrobial resistance ofJournal of medical microbiology · 2025
    Article
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  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

40 authors.

Stephanie W LoParasites and Microbes Programme, Wellcome Sanger Institute, Hinxton, UK. Electronic address: stephanie.lo@sanger.ac.uk.
Kate MellorParasites and Microbes Programme, Wellcome Sanger Institute, Hinxton, UK.
Robert CohenACTIV, Association Clinique et Thérapeutique Infantile du Val-de-Marne, Saint Maur-des-Fossés, France; GPIP, Groupe de Pathologie Infectieuse Pédiatrique, Paris, France; AFPA, Association Française de Pédiatrie Ambulatoire, Saint-Germain-en-Laye, France; Université Paris Est, IMRB-GRC GEMINI, Créteil, France; Clinical Research Center, Centre Hospitalier Intercommunal de Créteil, Créteil, France; Unité Court Séjour, Petits nourrissons, Service de Néonatalogie, Centre Hospitalier Intercommunal de Créteil, Créteil, France.
Alba Redin AlonsoDepartment of RDI Microbiology, Institut de Recerca Sant Joan de Deu, Hospital Sant Joan de Deu, Barcelona, Spain; School of Medicine, Universitat Internacional de Catalunya, Barcelona, Spain; Spanish Network of Epidemiology and Public Health, CIBERESP, Instituto de Salud Carlos III, Madrid, Spain.
Sophie BelmanParasites and Microbes Programme, Wellcome Sanger Institute, Hinxton, UK.
Narender KumarParasites and Microbes Programme, Wellcome Sanger Institute, Hinxton, UK.
Paulina A HawkinsRollins School Public Health, Emory University, Atlanta, GA, USA.
Rebecca A GladstoneDepartment of Biostatistics, Institute of Basic Medical Sciences, Faculty of Medicine, University of Oslo, Oslo, Norway.
Anne von GottbergCentre for Respiratory Diseases and Meningitis, National Institute for Communicable Diseases, Johannesburg, South Africa.
Balaji VeeraraghavanDepartment of Clinical Microbiology, Christian Medical College, Vellore, India.
K L RavikumarCentral Research Laboratory, Kempegowda Institute of Medical Sciences, Bangalore, India.
Rama KandasamyOxford Vaccine Group, Department of Paediatrics, University of Oxford, Churchill Hospital, Oxford, UK; NIHR Oxford Biomedical Research Centre, Oxford, UK; School of Women and Children's Health, University of New South Wales, Sydney, NSW, Australia; Discipline of Paediatrics and Child Health, School of Clinical Medicine, University of New South Wales, Sydney, NSW, Australia.
Sir Andrew J PollardOxford Vaccine Group, Department of Paediatrics, University of Oxford, Churchill Hospital, Oxford, UK; NIHR Oxford Biomedical Research Centre, Oxford, UK.
Samir K SahaChild Health Research Foundation, Dhaka, Bangladesh.
Godfrey BigogoKenya Medical Research Institute, Kisumu, Kenya.
Martin AntonioWHO Collaborating Centre for New Vaccines Surveillance, Medical Research Council Unit The Gambia at The London School of Hygiene & Tropical Medicine, Fajara, The Gambia.
Brenda Kwambana-AdamsWHO Collaborating Centre for New Vaccines Surveillance, Medical Research Council Unit The Gambia at The London School of Hygiene & Tropical Medicine, Fajara, The Gambia; NIHR Global Health Research Unit on Mucosal Pathogens, Division of Infection and Immunity, University College London, London, UK.
Shaper MirzaMicrobiology and Immunology Laboratory, Department of Biology, Lahore University of Management Sciences, Lahore, Pakistan.
Sadia ShakoorDepartment of Pediatrics and Child Health, Aga Khan University, Karachi, Pakistan.
Imran NisarDepartment of Pediatrics and Child Health, Aga Khan University, Karachi, Pakistan.
Jennifer E CornickMalawi-Liverpool-Wellcome-Trust, Blantyre, Malawi; Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, UK.
Deborah LehmannWesfarmers Centre of Vaccines and Infectious Diseases, Telethon Kids Institute, The University of Western Australia, Perth, WA, Australia.
Rebecca L FordPapua New Guinea Institute of Medical Research, Goroka, Papua New Guinea.
Betuel SigauqueCentro de Investigação em Saúde da Manhiça, Maputo, Mozambique.
Paul TurnerCambodia Oxford Medical Research Unit, Angkor Hospital for Children, Siem Reap, Cambodia; Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Jennifer MoïsiAgence de Médecine Préventive, Abidjan, Côte d'Ivoire.
Stephen K ObaroDivision of Pediatric Infectious Disease, University of Nebraska Medical Center Omaha, Omaha, NE, USA; International Foundation against Infectious Diseases in Nigeria, Abuja, Nigeria.
Ron DaganBen-Gurion University of the Negev, Beer-Sheva, Israel.
Idrissa DiawaraDepartment of Microbiology, Faculty of Medicine and Pharmacy of Casablanca, Hassan II University of Casablanca, Casablanca, Morocco; National Reference Laboratory, Mohammed VI University of Health Sciences, Casablanca, Morocco.
Anna SkoczyńskaDepartment of Epidemiology and Clinical Microbiology, National Medicines Institute, Warsaw, Poland.
Hui WangPeking University People 's Hospital, Beijing, China.
Philip E CarterInstitute of Environmental Science and Research Limited, Kenepuru Science Centre, Porirua, New Zealand.
Keith P KlugmanRollins School Public Health, Emory University, Atlanta, GA, USA.
Gail RodgersPneumonia Program, Bill & Melinda Gates Foundation, Seattle, WA, USA.
Robert F BreimanRollins School Public Health, Emory University, Atlanta, GA, USA; Emory Global Health Institute, Emory University, Atlanta, GA, USA.
Lesley McGeeCenters for Disease Control and Prevention, Atlanta, GA, USA.
Stephen D BentleyParasites and Microbes Programme, Wellcome Sanger Institute, Hinxton, UK.
Carmen Muñoz-AlmagroDepartment of RDI Microbiology, Institut de Recerca Sant Joan de Deu, Hospital Sant Joan de Deu, Barcelona, Spain; School of Medicine, Universitat Internacional de Catalunya, Barcelona, Spain; Spanish Network of Epidemiology and Public Health, CIBERESP, Instituto de Salud Carlos III, Madrid, Spain.
Emmanuelle VaronNational Reference Center for Pneumococci, Centre Hospitalier Intercommunal de Créteil, Créteil, France.
Global Pneumococcal Sequencing Consortium

Funding

Wellcome Trust
6 · The paper itself

Abstract

backgroundSerotype 24F is one of the emerging pneumococcal serotypes after the introduction of pneumococcal conjugate vaccine (PCV). We aimed to identify lineages driving the increase of serotype 24F in France and place these findings into a global context.

methodsWhole-genome sequencing was performed on a collection of serotype 24F pneumococci from asymptomatic colonisation (n=229) and invasive disease (n=190) isolates among individuals younger than 18 years in France, from 2003 to 2018. To provide a global context, we included an additional collection of 24F isolates in the Global Pneumococcal Sequencing (GPS) project database for analysis. A Global Pneumococcal Sequence Cluster (GPSC) and a clonal complex (CC) were assigned to each genome. Phylogenetic, evolutionary, and spatiotemporal analysis were conducted using the same 24F collection and supplemented with a global collection of genomes belonging to the lineage of interest from the GPS project database (n=25 590).

findingsSerotype 24F was identified in numerous countries mainly due to the clonal spread of three lineages: GPSC10 (CC230), GPSC16 (CC156), and GPSC206 (CC7701). GPSC10 was the only multidrug-resistant lineage. GPSC10 drove the increase in 24F in France and had high invasive disease potential. The international dataset of GPSC10 (n=888) revealed that this lineage expressed 16 other serotypes, with only six included in 13-valent PCV (PCV13). All serotype 24F isolates were clustered in a single clade within the GPSC10 phylogeny and long-range transmissions were detected from Europe to other continents. Spatiotemporal analysis showed GPSC10-24F took 3-5 years to spread across France and a rapid change of serotype composition from PCV13 serotype 19A to 24F during the introduction of PCV13 was observed in neighbouring country Spain.

interpretationOur work reveals that GPSC10 alone is a challenge for serotype-based vaccine strategy. More systematic investigation to identify lineages like GPSC10 will better inform and improve next-generation preventive strategies against pneumococcal diseases.

fundingBill & Melinda Gates Foundation, Wellcome Sanger Institute, and the US Centers for Disease Control and Prevention.

Indexed as

Pneumococcal InfectionsStreptococcus pneumoniaeHumansPhylogenySerogroupVaccines, ConjugateVaccines, Conjugate

Identifiers

PMID35985351
PMCPMC9519462

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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.