Evidence map›Paper›PMID 25266387›Full record

ArticleJournal of bacteriology2014

A genetic screen in Myxococcus xanthus identifies mutants that uncouple outer membrane exchange from a downstream cellular response.

Arup Dey, Daniel Wall

Open access · bronzeAbstract read
In one paragraph

Article in Journal of bacteriology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

23 citing papers in PubMed, 32 citations in OpenAlex.

  1. Deep learning framework for quantifying self-organization inProceedings of the National Academy of Sciences of the United States of America · 2026
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  2. Functional Cargo in Membrane Vesicles From a Citrus Pathogen.Environmental microbiology reports · 2025
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  6. Applied and environmental microbiology · 2024
    Article
  7. Cell-cell transfer of adaptation traits benefits kin and actor in a cooperative microbe.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  8. Loratadine Combats Methicillin-ResistantACS infectious diseases · 2024
    Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Self-identity barcodes encoded by six expansive polymorphic toxin families discriminate kin in myxobacteria.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Tissue repair in myxobacteria: A cooperative strategy to heal cellular damage.BioEssays : news and reviews in molecular, cellular and developmental biology · 2016
    Article
  19. Article
  20. 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

2 authors at 1 institution in 1 country.

Arup DeyDepartment of Molecular Biology, University of Wyoming, Laramie, Wyoming, USA.
Daniel WallDepartment of Molecular Biology, University of Wyoming, Laramie, Wyoming, USA dwall2@uwyo.edu.
University of Wyoming · US

Funding

Protein exchange and self recognition in myxobacteria biofilmsR01GM101449 · NIGMS · UNIVERSITY OF WYOMING · PI WALL, DANIEL · 2012 to 2020
$2.6M
NIGMS NIH HHS GM101449NIGMS NIH HHS R01 GM101449
6 · The paper itself

Abstract

Upon physical contact with sibling cells, myxobacteria transiently fuse their outer membranes (OMs) and exchange OM proteins and lipids. From previous work, TraA and TraB were identified to be essential factors for OM exchange (OME) in donor and recipient cells. To define the genetic complexity of OME, we carried out a comprehensive forward genetic screen. The screen was based on the observation that Myxococcus xanthus nonmotile cells, by a Tra-dependent mechanism, block swarm expansion of motile cells when mixed. Thus, mutants defective in OME or a downstream responsive pathway were readily identified as escape flares from mixed inocula seeded on agar. This screen was surprisingly powerful, as we found >50 mutants defective in OME. Importantly, all of the mutations mapped to the traAB operon, suggesting that there may be few, if any, proteins besides TraA and TraB directly required for OME. We also found a second and phenotypically different class of mutants that exhibited wild-type OME but were defective in a responsive pathway. This pathway is postulated to control inner membrane homeostasis by covalently attaching amino acids to phospholipids. The identified proteins are homologous to the Staphylococcus aureus MprF protein, which is involved in membrane adaptation and antibiotic resistance. Interestingly, we also found that a small number of nonmotile cells were sufficient to block the swarming behavior of a large gliding-proficient population. This result suggests that an OME-derived signal could be amplified from a few nonmotile producers to act on many responder cells.

Indexed as

Gene Expression Regulation, BacterialSignal TransductionBacterial Outer Membrane ProteinsGenetic TestingLocomotionMembrane LipidsMutationMyxococcus xanthusSequence HomologyBacterial Outer Membrane ProteinsMembrane Lipids

Identifiers

PMID25266387
PMCPMC4248844
OpenAlexW1978525114

What OpenQuestion holds

Textmetadata
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.