Evidence map›Paper›PMID 31119276›Full record

ArticleThe Journal of infectious diseases2019

Potentiation of Phase Variation in Multiple Outer-Membrane Proteins During Spread of the Hyperinvasive Neisseria meningitidis Serogroup W ST-11 Lineage.

Luke R Green, Neelam Dave, Adeolu B Adewoye, Jay Lucidarme, Stephen A Clark, Neil J Oldfield, David P J Turner, Ray Borrow, Christopher D Bayliss

Abstract read
In one paragraph

Article in The Journal of infectious diseases, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Rapid and recent evolution ofMicrobial genomics · 2026
    Article
  3. Article
  4. Article
  5. Variable disruption of epithelial monolayers byMicrobiology (Reading, England) · 2023
    Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. Article
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.

Luke R GreenDepartment of Genetics and Genome Biology, University of Leicester, Leicester.
Neelam DaveDepartment of Genetics and Genome Biology, University of Leicester, Leicester.
Adeolu B AdewoyeDepartment of Genetics and Genome Biology, University of Leicester, Leicester.
Jay LucidarmeMeningococcal Reference Unit, Public Health England, Manchester Royal Infirmary, Manchester.
Stephen A ClarkMeningococcal Reference Unit, Public Health England, Manchester Royal Infirmary, Manchester.
Neil J OldfieldSchool of Life Sciences, University of Nottingham, Nottingham, United Kingdom.
David P J TurnerSchool of Life Sciences, University of Nottingham, Nottingham, United Kingdom.
Ray BorrowMeningococcal Reference Unit, Public Health England, Manchester Royal Infirmary, Manchester.
Christopher D BaylissDepartment of Genetics and Genome Biology, University of Leicester, Leicester.

Funding

Medical Research Council MR/M020193/1
6 · The paper itself

Abstract

backgroundSince 2009, increases in the incidence of invasive meningococcal disease have occurred in the United Kingdom due to a sublineage of the Neisseria meningitidis serogroup W ST-11 clonal complex (hereafter, the "original UK strain"). In 2013, a descendent substrain (hereafter, the "2013 strain") became the dominant disease-causing variant. Multiple outer-membrane proteins of meningococci are subject to phase-variable switches in expression due to hypermutable simple-sequence repeats. We investigated whether alterations in phase-variable genes may have influenced the relative prevalence of the original UK and 2013 substrains, using multiple disease and carriage isolates.

methodsRepeat numbers were determined by either bioinformatics analysis of whole-genome sequencing data or polymerase chain reaction amplification and sizing of fragments from genomic DNA extracts. Immunoblotting and sequence-translation analysis was performed to identify expression states.

resultsSignificant increases in repeat numbers were detected between the original UK and 2013 strains in genes encoding PorA, NadA, and 2 Opa variants. Invasive and carriage isolates exhibited similar repeat numbers, but the absence of pilC gene expression was frequently associated with disease.

conclusionsElevated repeat numbers in outer-membrane protein genes of the 2013 strain are indicative of higher phase-variation rates, suggesting that rapid expansion of this strain was due to a heightened ability to evade host immune responses during transmission and asymptomatic carriage.

Indexed as

Genetic VariationAdhesins, BacterialBacterial Outer Membrane ProteinsDNA, BacterialFimbriae ProteinsGene Expression Regulation, BacterialMeningococcal InfectionsMicrosatellite RepeatsMolecular EpidemiologyNeisseria meningitidisPorinsSequence Analysis, DNASerogroupUnited KingdomWhole Genome SequencingAdhesins, BacterialBacterial Outer Membrane ProteinsDNA, BacterialFimbriae ProteinsNadA protein, Neisseria meningitidisOpa protein, Neisseriaporin protein, NeisseriaPorinsNadANeisseria meningitidisOpaphase variationserogroup Wsimple sequence repeat

Identifiers

PMID31119276
PMCPMC6735796

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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.