Publication

Putative novel cps loci in a large global collection of pneumococci

Downloadable Content

Persistent URL
Last modified
  • 05/15/2025
Type of Material
Authors
    Andries J. van Tonder, Wellcome Sanger InstituteRebecca A. Gladstone, Wellcome Sanger InstituteStephanie W. Lo, Wellcome Sanger InstituteMoon H. Nahm, University of Alabama BirminghamMignon du Plessis, National Institute for Communicable DiseasesJennifer Cornick, Malawi-Liverpool-Wellcome-TrustBrenda Kwambana-Adams, MRC UnitShabir A. Madhi, University of WitwatersrandPaulina A. Hawkins, Emory UniversityRachel Benisty, Ben-Gurion University of the NegevRon Dagan, Ben-Gurion University of the NegevDean Everett, University of EdinburghKeith P Klugman, Emory UniversityMartin Antonio, MRC UnitAnne von Gottberg, National Institute for Communicable DiseasesRobert F Breiman, Emory UniversityLesley McGee, Centers for Disease Control and PreventionStephen D. Bentley, Wellcome Sanger Institute
Language
  • English
Date
  • 2019-07-01
Publisher
  • Microbiology Society: Microbial Genomics
Publication Version
Copyright Statement
  • © 2019 The Authors.
License
Final Published Version (URL)
Title of Journal or Parent Work
ISSN
  • 2057-5858
Volume
  • 5
Issue
  • 7
Grant/Funding Information
  • This study was co-funded by the Bill and Melinda Gates Foundation (grant code OPP1034556); the Wellcome Sanger Institute (core Wellcome grants 098051 and 206194); and the US Centers for Disease Control and Prevention.
Supplemental Material (URL)
Abstract
  • The pneumococcus produces a polysaccharide capsule, encoded by the cps locus, that provides protection against phagocytosis and determines serotype. Nearly 100 serotypes have been identified with new serotypes still being discovered, especially in previously understudied regions. Here we present an analysis of the cps loci of more than 18 000 genomes from the Global Pneumococcal Sequencing (GPS) project with the aim of identifying novel cps loci with the potential to produce previously unrecognized capsule structures. Serotypes were assigned using whole genome sequence data and 66 of the approximately 100 known serotypes were included in the final dataset. Closer examination of each serotype’s sequences identified nine putative novel cps loci (9X, 11X, 16X, 18X1, 18X2, 18X3, 29X, 33X and 36X) found in ~2.6 % of the genomes. The large number and global distribution of GPS genomes provided an unprecedented opportunity to identify novel cps loci and consider their phylogenetic and geographical distribution. Nine putative novel cps loci were identified and examples of each will undergo subsequent structural and immunological analysis.
Author Notes
Keywords
Research Categories
  • Biology, Microbiology
  • Health Sciences, Public Health

Tools

Relations

In Collection:

Items