Evidence map›Paper›PMID 24797914›Full record

ArticlePloS one2014

Type IV pilus assembly proficiency and dynamics influence pilin subunit phospho-form macro- and microheterogeneity in Neisseria gonorrhoeae.

Åshild Vik, Jan Haug Anonsen, Finn Erik Aas, Finn Terje Hegge, Norbert Roos, Michael Koomey, Marina Aspholm

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 42% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Review
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

7 authors at 1 institution in 1 country.

Åshild VikCentre for Molecular Biology and Neuroscience, University of Oslo, Oslo, Norway; Department of Biosciences, University of Oslo, Oslo, Norway.
Jan Haug AnonsenCentre for Molecular Biology and Neuroscience, University of Oslo, Oslo, Norway; Department of Biosciences, University of Oslo, Oslo, Norway.
Finn Erik AasCentre for Molecular Biology and Neuroscience, University of Oslo, Oslo, Norway; Department of Biosciences, University of Oslo, Oslo, Norway.
Finn Terje HeggeCentre for Molecular Biology and Neuroscience, University of Oslo, Oslo, Norway; Department of Biosciences, University of Oslo, Oslo, Norway.
Norbert RoosCentre for Molecular Biology and Neuroscience, University of Oslo, Oslo, Norway.
Michael KoomeyCentre for Molecular Biology and Neuroscience, University of Oslo, Oslo, Norway; Department of Biosciences, University of Oslo, Oslo, Norway.
Marina AspholmCentre for Molecular Biology and Neuroscience, University of Oslo, Oslo, Norway; Department of Biosciences, University of Oslo, Oslo, Norway.
University of Oslo · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The PilE pilin subunit protein of the gonococcal Type IV pilus (Tfp) colonization factor undergoes multisite, covalent modification with the zwitterionic phospho-form modification phosphoethanolamine (PE). In a mutant lacking the pilin-like PilV protein however, PilE is modified with a mixture of PE and phosphocholine (PC). Moreover, intrastrain variation of PilE PC modification levels have been observed in backgrounds that constitutively express PptA (the protein phospho-form transferase A) required for both PE and PC modification. The molecular basis underlying phospho-form microheterogeneity in these instances remains poorly defined. Here, we examined the effects of mutations at numerous loci that disrupt or perturb Tfp assembly and observed that these mutants phenocopy the pilV mutant vis a vis phospho-form modification status. Thus, PC modification appears to be directly or indirectly responsive to the efficacy of pilin subunit interactions. Despite the complexity of contributing factors identified here, the data favor a model in which increased retention in the inner membrane may act as a key signal in altering phospho-form modification. These results also provide an alternative explanation for the variation in PilE PC levels observed previously and that has been assumed to be due to phase variation of pptA. Moreover, mass spectrometry revealed evidence for mono- and di-methylated forms of PE attached to PilE in mutants deficient in pilus assembly, directly implicating a methyltransferase-based pathway for PC synthesis in N. gonorrhoeae.

Indexed as

Chromatography, LiquidElectrophoresis, Polyacrylamide GelEthanolaminesFimbriae ProteinsGene Expression Regulation, BacterialGlycosylationImmunoblottingMass SpectrometryModels, MolecularMutation, MissenseNeisseria gonorrhoeaePhosphorylcholinePili, SexProtein Processing, Post-TranslationalEthanolaminesFimbriae ProteinsPhosphorylcholinephosphorylethanolaminepilE protein, Neisseria gonorrhoeae

Identifiers

PMID24797914
PMCPMC4010543
OpenAlexW2035426453

What OpenQuestion holds

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LicenceCC BY
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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.