Evidence map›Paper›PMID 26492862›Full record

ArticleScientific reports2015

The post-vaccine microevolution of invasive Streptococcus pneumoniae.

Amelieke J H Cremers, Fredrick M Mobegi, Marien I de Jonge, Sacha A F T van Hijum, Jacques F Meis, Peter W M Hermans, Gerben Ferwerda, Stephen D Bentley, Aldert L Zomer

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
4.6field-weighted citation impact, top 5% 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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 47 citations in OpenAlex.

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  20. Nosocomial outbreak of multi-resistantAntimicrobial resistance and infection control · 2018
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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

9 authors at 4 institutions in 2 countries.

Amelieke J H CremersRadboud university medical center, Laboratory of Pediatric Infectious Diseases, Nijmegen, The Netherlands.
Fredrick M MobegiRadboud university medical center, Laboratory of Pediatric Infectious Diseases, Nijmegen, The Netherlands.
Marien I de JongeRadboud university medical center, Laboratory of Pediatric Infectious Diseases, Nijmegen, The Netherlands.
Sacha A F T van HijumRadboud university medical center, Bacterial Genomics Group; Center for Molecular and Biomolecular Informatics, Nijmegen, The Netherlands.
Jacques F MeisCanisius-Wilhelmina Hospital, Department of Medical Microbiology and Infectious Diseases, Nijmegen, The Netherlands.
Peter W M HermansRadboud university medical center, Laboratory of Pediatric Infectious Diseases, Nijmegen, The Netherlands.
Gerben FerwerdaRadboud university medical center, Laboratory of Pediatric Infectious Diseases, Nijmegen, The Netherlands.
Stephen D BentleyWellcome Trust Sanger Institute, Pathogen Genomics group, Hinxton Cambridge, United Kingdom.
Aldert L ZomerRadboud university medical center, Laboratory of Pediatric Infectious Diseases, Nijmegen, The Netherlands.
Radboud University Medical Center · NLRadboud University Nijmegen · NLCanisius-Wilhelmina Ziekenhuis · NLWellcome Sanger Institute · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The 7-valent pneumococcal conjugated vaccine (PCV7) has affected the genetic population of Streptococcus pneumoniae in pediatric carriage. Little is known however about pneumococcal population genomics in adult invasive pneumococcal disease (IPD) under vaccine pressure. We sequenced and serotyped 349 strains of S. pneumoniae isolated from IPD patients in Nijmegen between 2001 and 2011. Introduction of PCV7 in the Dutch National Immunization Program in 2006 preluded substantial alterations in the IPD population structure caused by serotype replacement. No evidence could be found for vaccine induced capsular switches. We observed that after a temporary bottleneck in gene diversity after the introduction of PCV7, the accessory gene pool re-expanded mainly by genes already circulating pre-PCV7. In the post-vaccine genomic population a number of genes changed frequency, certain genes became overrepresented in vaccine serotypes, while others shifted towards non-vaccine serotypes. Whether these dynamics in the invasive pneumococcal population have truly contributed to invasiveness and manifestations of disease remains to be further elucidated. We suggest the use of whole genome sequencing for surveillance of pneumococcal population dynamics that could give a prospect on the course of disease, facilitating effective prevention and management of IPD.

Indexed as

Biological EvolutionGenome, BacterialHeptavalent Pneumococcal Conjugate VaccineStreptococcus pneumoniaeHeptavalent Pneumococcal Conjugate Vaccine

Identifiers

PMID26492862
PMCPMC4615977
OpenAlexW2182790945

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.