Evidence map›Paper›PMID 25972423›Full record

ArticleJournal of clinical microbiology2015

Genomics Reveals the Worldwide Distribution of Multidrug-Resistant Serotype 6E Pneumococci.

Andries J van Tonder, James E Bray, Lucy Roalfe, Rebecca White, Marta Zancolli, Sigríður J Quirk, Gunnsteinn Haraldsson, Keith A Jolley, Martin C J Maiden, Stephen D Bentley and 5 more

Erratum issuedAbstract read
In one paragraph

Article in Journal of clinical microbiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–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

18 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

Andries J van TonderNuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.
James E BrayDepartment of Zoology, University of Oxford, Oxford, United Kingdom.
Lucy RoalfeInstitute of Child Health, University College London, London, United Kingdom.
Rebecca WhiteInstitute of Child Health, University College London, London, United Kingdom.
Marta ZancolliInstitute of Child Health, University College London, London, United Kingdom.
Sigríður J QuirkUniversity of Iceland, Reykjavik, Iceland Landspitali University Hospital, Reykjavik, Iceland.
Gunnsteinn HaraldssonUniversity of Iceland, Reykjavik, Iceland Landspitali University Hospital, Reykjavik, Iceland.
Keith A JolleyDepartment of Zoology, University of Oxford, Oxford, United Kingdom.
Martin C J MaidenDepartment of Zoology, University of Oxford, Oxford, United Kingdom.
Stephen D BentleyPathogen Genomics, Wellcome Trust Sanger Institute, Hinxton, United Kingdom.
Ásgeir HaraldssonUniversity of Iceland, Reykjavik, Iceland Landspitali University Hospital, Reykjavik, Iceland.
Helga ErlendsdóttirUniversity of Iceland, Reykjavik, Iceland Landspitali University Hospital, Reykjavik, Iceland.
Karl G KristinssonUniversity of Iceland, Reykjavik, Iceland Landspitali University Hospital, Reykjavik, Iceland.
David GoldblattInstitute of Child Health, University College London, London, United Kingdom.
Angela B BrueggemannNuffield Department of Medicine, University of Oxford, Oxford, United Kingdom angela.brueggemann@ndm.ox.ac.uk.

Funding

Wellcome Trust 04992/Z/14/ZWellcome Trust 083511/Z/07/ZWellcome Trust 087622Wellcome Trust 100891
6 · The paper itself

Abstract

The pneumococcus is a leading pathogen infecting children and adults. Safe, effective vaccines exist, and they work by inducing antibodies to the polysaccharide capsule (unique for each serotype) that surrounds the cell; however, current vaccines are limited by the fact that only a few of the nearly 100 antigenically distinct serotypes are included in the formulations. Within the serotypes, serogroup 6 pneumococci are a frequent cause of serious disease and common colonizers of the nasopharynx in children. Serotype 6E was first reported in 2004 but was thought to be rare; however, we and others have detected serotype 6E among recent pneumococcal collections. Therefore, we analyzed a diverse data set of ∼1,000 serogroup 6 genomes, assessed the prevalence and distribution of serotype 6E, analyzed the genetic diversity among serogroup 6 pneumococci, and investigated whether pneumococcal conjugate vaccine-induced serotype 6A and 6B antibodies mediate the killing of serotype 6E pneumococci. We found that 43% of all genomes were of serotype 6E, and they were recovered worldwide from healthy children and patients of all ages with pneumococcal disease. Four genetic lineages, three of which were multidrug resistant, described ∼90% of the serotype 6E pneumococci. Serological assays demonstrated that vaccine-induced serotype 6B antibodies were able to elicit killing of serotype 6E pneumococci. We also revealed three major genetic clusters of serotype 6A capsular sequences, discovered a new hybrid 6C/6E serotype, and identified 44 examples of serotype switching. Therefore, while vaccines appear to offer protection against serotype 6E, genetic variants may reduce vaccine efficacy in the longer term because of the emergence of serotypes that can evade vaccine-induced immunity.

Indexed as

Genetic VariationGenotypeMolecular TypingSerogroupAdolescentAdultAgedBlood Bactericidal ActivityChildChild, PreschoolFemaleGlobal HealthHumansInfantMaleMiddle AgedPneumococcal Vaccines

Identifiers

PMID25972423
PMCPMC4473186

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Registered trials

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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.