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Visualizing variation within global pneumococcal sequence clusters (GPSCS) and country population snapshots to contextualize pneumococcal isolates

  • Rebecca A. Gladstone
  • , Stephanie W. Lo
  • , Richard Goater
  • , Corin Yeats
  • , Ben Taylor
  • , James Hadfield
  • , John A. Lees
  • , Nicholas J. Croucher
  • , Andries J. van Tonder
  • , Leon J. Bentley
  • , Fu Xiang Quah
  • , Anne J. Blaschke
  • , Nicole L. Pershing
  • , Carrie L. Byington
  • , Veeraraghavan Balaji
  • , Waleria Hryniewicz
  • , Betuel Sigauque
  • , K. L. Ravikumar
  • , Samanta Cristine Grassi Almeida
  • , Theresa J. Ochoa
  • Pak Leung Ho, Mignon du Plessis, Kedibone M. Ndlangisa, Jennifer E. Cornick, Brenda Kwambana-Adams, Rachel Benisty, Susan A. Nzenze, Shabir A. Madhi, Paulina A. Hawkins, Andrew J. Pollard, Dean B. Everett, Martin Antonio, Ron Dagan, Keith P. Klugman, Anne von Gottberg, Benjamin J. Metcalf, Yuan Li, Bernard W. Beall, Lesley McGee, Robert F. Breiman, David M. Aanensen, Stephen D. Bentley, Patrick E. Akpaka, Krow Ampofo, Houria Belabbès, Godfrey Bigogo, Abdullah W. Brooks, Philip E. Carter, Stuart C. Clarke, Alejandra Corso, Maria Cristina de Cunto Brandileone, Alexander Davydov, Idrissa Diawara, Sanjay Doiphode, Ekaterina Egorova, Naima Elmdaghri, Özgen Köseoglu Eser, Diego Faccone, Rebecca Ford, Paula Gagetti, Noga Givon-Lavi, Md Hasanuzzaman, Kristina G. Hulten, Margaret Ip, Aurelie Kapusta, Rama Kandasamy, Tamara Kastrin, Jeremy Keenan, Pierra Y. Law, Deborah Lehmann, Jennifer Moïsi, Helio Mucavele, Michele Nurse-Lucas, Stephen K. Obaro, Metka Paragi, Ewa Sadowy, Samir K. Saha, Eric Sampane-Donkor, Shamala Devi Sekaran, Sadia Shakoor, Shrijana Shrestha, Anna Skoczynska, Soo Ko, Somporn Srifuengfung, Peggy Estelle Tientcheu, Leonid Titov, Paul Turner, Yulia Urban, Jennifer Verani, Elena Voropaeva, Nicole Wolter
  • Parasites and microbes
  • Centre for Genomic Pathogen Surveillance
  • Nuffield Department of Medicine
  • Fred Hutchinson Cancer Research Center
  • Imperial College London
  • University of Cambridge
  • University of Utah
  • University of California
  • Christian Medical College, Vellore
  • National Medicines Institute, Warsaw
  • Centro de Investigação em Saúde da Manhiça
  • Kempegowda Institute of Medical Sciences
  • Adolfo Lutz Institute
  • Universidad Peruana Cayetano Heredia
  • University of Hong Kong
  • National Institute for Communicable Diseases
  • Malawi-Liverpool-Wellcome Trust Clinical Research Programme
  • University College London
  • London School of Hygiene and Tropical Medicine
  • Ben-Gurion University of the Negev
  • University of the Witwatersrand, Johannesburg
  • Rollins School of Public Health
  • University of Oxford Medical Sciences Division
  • Centers for Disease Control and Prevention
  • Emory University
  • The University of the West Indies, St. Augustine Campus
  • University Hospital Centre Ibn Rochd
  • Kenya Medical Research Institute
  • International Centre for Diarrheal Diseases Research
  • Kenepuru Science Centre
  • University of Southampton, Faculty of Medicine
  • Instituto Nacional de Enfermedades Infecciosas
  • Belarusian State Medical University
  • The Republican Research and Practical Center for Epidemiology and Microbiology
  • Mohammed VI University of Health Sciences (UM6SS)
  • Oral Health Institute Hamad Medical Corporation
  • G. N. Gabrichevsky Research Institute for Epidemiology and Microbiology
  • Hacettepe University Faculty of Medicine
  • Papua New Guinea Institute of Medical Research
  • Dhaka Shishu Hospital
  • Baylor College of Medicine
  • Chinese University of Hong Kong
  • NIHR Oxford Biomedical Research Centre
  • Institute of Public Health of the Republic of Slovenia
  • University of California, San Francisco
  • Telethon Kids Institute
  • Agence de Médecine Préventive
  • University of Nebraska Medical Center
  • National Laboratory of Health
  • Child Health Research Foundation
  • University of Ghana
  • MAHSA University
  • Aga Khan University
  • Patan Academy of Health Sciences
  • Sungkyunkwan University School of Medicine
  • Mahidol University
  • MRC Unit
  • Centers for Disease Control and Prevention

Research output: Contribution to journalArticlepeer-review

50 Scopus citations

Abstract

Knowledge of pneumococcal lineages, their geographic distribution and antibiotic resistance patterns, can give insights into global pneumococcal disease. We provide interactive bioinformatic outputs to explore such topics, aiming to increase dissemi-nation of genomic insights to the wider community, without the need for specialist training. We prepared 12 country-specific phylogenetic snapshots, and international phylogenetic snapshots of 73 common Global Pneumococcal Sequence Clusters (GPSCs) previously defined using PopPUNK, and present them in Microreact. Gene presence and absence defined using Roary, and recombination profiles derived from Gubbins are presented in Phandango for each GPSC. Temporal phylogenetic signal was assessed for each GPSC using BactDating. We provide examples of how such resources can be used. In our example use of a country-specific phylogenetic snapshot we determined that serotype 14 was observed in nine unrelated genetic backgrounds in South Africa. The international phylogenetic snapshot of GPSC9, in which most serotype 14 isolates from South Africa were observed, highlights that there were three independent sub-clusters represented by South African serotype 14 isolates. We estimated from the GPSC9-dated tree that the sub-clusters were each established in South Africa during the 1980s. We show how recombination plots allowed the identification of a 20 kb recombination spanning the capsular polysaccharide locus within GPSC97. This was consistent with a switch from serotype 6A to 19A estimated to have occured in the 1990s from the GPSC97-dated tree. Plots of gene presence/absence of resistance genes (tet, erm, cat) across the GPSC23 phylogeny were consistent with acquisition of a composite transposon. We estimated from the GPSC23-dated tree that the acquisition occurred between 1953 and 1975. Finally, we demonstrate the assignment of GPSC31 to 17 externally generated pneumococcal serotype 1 assemblies from Utah via Pathogenwatch. Most of the Utah isolates clustered within GPSC31 in a USA-specific clade with the most recent common ancestor estimated between 1958 and 1981. The resources we have provided can be used to explore to data, test hypothesis and generate new hypotheses. The accessible assignment of GPSCs allows others to contextualize their own collections beyond the data presented here.

Original languageBritish English
Article number000357
Pages (from-to)1-13
Number of pages13
JournalMicrobial Genomics
Volume6
Issue number5
DOIs
StatePublished - 2020

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being
  2. SDG 4 - Quality Education
    SDG 4 Quality Education

Keywords

  • Antibiotic resistance
  • Pangenome
  • Phylogenetic dating
  • Pneumococcal
  • Population structure
  • Recombination
  • Streptococcus pneumoniae
  • Whole genome sequencing

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