Evidence map›Paper›PMID 35536022›Full record

ArticleMicrobiology spectrum2022

Pneumococcal Phasevarions Control Multiple Virulence Traits, Including Vaccine Candidate Expression.

Zachary N Phillips, Claudia Trappetti, Annelies Van Den Bergh, Gael Martin, Ainslie Calcutt, Victoria Ozberk, Patrice Guillon, Manisha Pandey, Mark von Itzstein, W Edward Swords and 3 more

Open access · goldAbstract read
In one paragraph

Article in Microbiology spectrum, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

11 citing papers in PubMed, 14 citations in OpenAlex.

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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

13 authors at 3 institutions in 2 countries.

Zachary N PhillipsInstitute for Glycomics, Griffith Universitygrid.1022.1, Queensland, Australia.
Claudia TrappettiResearch Centre for Infectious Diseases, Department of Molecular and Biomedical Science, University of Adelaidegrid.1010.0, Adelaide, Australia.
Annelies Van Den BerghInstitute for Glycomics, Griffith Universitygrid.1022.1, Queensland, Australia.
Gael MartinInstitute for Glycomics, Griffith Universitygrid.1022.1, Queensland, Australia.
Ainslie CalcuttInstitute for Glycomics, Griffith Universitygrid.1022.1, Queensland, Australia.
Victoria OzberkInstitute for Glycomics, Griffith Universitygrid.1022.1, Queensland, Australia.
Patrice GuillonInstitute for Glycomics, Griffith Universitygrid.1022.1, Queensland, Australia.
Manisha PandeyInstitute for Glycomics, Griffith Universitygrid.1022.1, Queensland, Australia.
Mark von ItzsteinInstitute for Glycomics, Griffith Universitygrid.1022.1, Queensland, Australia.ORCID 0000-0001-6302-7524
W Edward SwordsDepartment of Medicine, Division of Pulmonary, Allergy, and Critical Care Medicine, University of Alabama at Birminghamgrid.265892.2, Birmingham, Alabama, USA.ORCID 0000-0003-4063-940X
James C PatonResearch Centre for Infectious Diseases, Department of Molecular and Biomedical Science, University of Adelaidegrid.1010.0, Adelaide, Australia.ORCID 0000-0001-9807-5278
Michael P JenningsInstitute for Glycomics, Griffith Universitygrid.1022.1, Queensland, Australia.ORCID 0000-0002-1027-4684
John M AtackInstitute for Glycomics, Griffith Universitygrid.1022.1, Queensland, Australia.ORCID 0000-0002-7994-6995
Griffith University · AUThe University of Adelaide · AUUniversity of Alabama at Birmingham · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Streptococcus pneumoniae is the most common cause of bacterial illness worldwide. Current vaccines based on the polysaccharide capsule are only effective against a limited number of the >100 capsular serotypes. A universal vaccine based on conserved protein antigens requires a thorough understanding of gene expression in S. pneumoniae. All S. pneumoniae strains encode the SpnIII Restriction-Modification system. This system contains a phase-variable methyltransferase that switches specificity, and controls expression of multiple genes-a phasevarion. We examined the role of this phasevarion during pneumococcal pathobiology, and determined if phase variation resulted in differences in expression of currently investigated conserved protein antigens. Using locked strains that express a single methyltransferase specificity, we found differences in clinically relevant traits, including survival in blood, and adherence to and invasion of human cells. We also observed differences in expression of numerous proteinaceous vaccine candidates, which complicates selection of antigens for inclusion in a universal protein-based pneumococcal vaccine. This study will inform vaccine design against S. pneumoniae by ensuring only stably expressed candidates are included in a rationally designed vaccine.

Indexed as

Phase VariationStreptococcus pneumoniaeHumansMethyltransferasesPneumococcal VaccinesVirulenceMethyltransferasesPneumococcal Vaccinesepigenetic regulationphase variationphasevarionpneumococcusStreptococcus pneumoniaevaccine

Identifiers

PMID35536022
PMCPMC9241608
OpenAlexW4229460004

What OpenQuestion holds

Textmetadata
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.