Evidence map›Paper›PMID 25404340›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2014

Global discovery of colonization determinants in the squid symbiont Vibrio fischeri.

John F Brooks, Mattias C Gyllborg, David C Cronin, Sarah J Quillin, Celeste A Mallama, Randi Foxall, Cheryl Whistler, Andrew L Goodman, Mark J Mandel

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 89 papers.

0numbers the graph read from it
0cells of the map it votes in
89citing 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

89 citing papers in PubMed.

  1. Sedative choice altersInfection and immunity · 2026
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  3. Review
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  5. mBio · 2025
    Article
  6. MutantMicrobiology spectrum · 2025
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  7. A single point mutation is sufficient to driveJournal of bacteriology · 2025
    Article
  8. Article
  9. Applied and environmental microbiology · 2025
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Functional analysis of cyclic diguanylate-modulating proteins inbioRxiv : the preprint server for biology · 2024
    Article
  18. Article
  19. Article
  20. Corrected and republished from: "Applied and environmental microbiology · 2024
    Article

29 more citing papers are in PubMed but not listed here.

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.

John F BrooksDepartment of Microbiology-Immunology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611;
Mattias C GyllborgDepartment of Microbiology-Immunology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611;
David C CroninDepartment of Microbiology-Immunology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611;
Sarah J QuillinDepartment of Microbiology-Immunology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611;
Celeste A MallamaDepartment of Microbiology-Immunology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611;
Randi FoxallDepartment of Molecular, Cellular, and Biomedical Sciences, University of New Hampshire, Durham, NH 03824; and.
Cheryl WhistlerDepartment of Molecular, Cellular, and Biomedical Sciences, University of New Hampshire, Durham, NH 03824; and.
Andrew L GoodmanDepartment of Microbial Pathogenesis and Microbial Sciences Institute, Yale University, New Haven, CT 06536.
Mark J MandelDepartment of Microbiology-Immunology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611; m-mandel@northwestern.edu.

Funding

CELLULAR &MOLECULAR BASIS OF DISEASE TRAINING PROGRAMT32GM008061 · NIGMS · NORTHWESTERN UNIVERSITY · PI CARTHEW, RICHARD W. · 1985 to 2022
$17.1M
Mentoring For Success: Developing Fundamental Skills For Biomedical ResearchR25GM079300 · NIGMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI MCGEE, RICHARD · 2007 to 2020
$6.6M
University of Michigan Postbaccalaureate Research Education Program (UM PREP)R25GM086262 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ALLEN, BENJAMIN · 2009 to 2024
$6.1M
Corrinoid Response of the Human Gut MicrobiotaK01DK089121 · NIDDK · YALE UNIVERSITY · PI GOODMAN, ANDREW L · 2010 to 2014
$597k
NIDDK NIH HHS DK089121NIDDK NIH HHS K01 DK089121NIGMS NIH HHS GM08061NIGMS NIH HHS R25 GM079300NIGMS NIH HHS R25 GM086262NIGMS NIH HHS T32 GM008061
6 · The paper itself

Abstract

Animal epithelial tissue becomes reproducibly colonized by specific environmental bacteria. The bacteria (microbiota) perform critical functions for the host's tissue development, immune system development, and nutrition; yet the processes by which bacterial diversity in the environment is selected to assemble the correct communities in the host are unclear. To understand the molecular determinants of microbiota selection, we examined colonization of a simplified model in which the light organ of Euprymna scolopes squid is colonized exclusively by Vibrio fischeri bacteria. We applied high-throughput insertion sequencing to identify which bacterial genes are required during host colonization. A library of over 41,000 unique transposon insertions was analyzed before and after colonization of 1,500 squid hatchlings. Mutants that were reproducibly depleted following squid colonization represented 380 genes, including 37 that encode known colonization factors. Validation of select mutants in defined competitions against the wild-type strain identified nine mutants that exhibited a reproducible colonization defect. Some of the colonization factors identified included genes predicted to influence copper regulation and secretion. Other mutants exhibited defects in biofilm development, which is required for aggregation in host mucus and initiation of colonization. Biofilm formation in culture and in vivo was abolished in a strain lacking the cytoplasmic chaperone DnaJ, suggesting an important role for protein quality control during the elaboration of bacterial biofilm in the context of an intact host immune system. Overall these data suggest that cellular stress responses and biofilm regulation are critical processes underlying the reproducible colonization of animal hosts by specific microbial symbionts.

Indexed as

Aliivibrio fischeriAnimalsBacterial ProteinsBiofilmsDecapodiformesDNA Transposable ElementsGene Expression Regulation, BacterialGenes, BacterialHigh-Throughput Nucleotide SequencingHost-Pathogen InteractionsMicrobiotaMutagenesis, InsertionalReverse Transcriptase Polymerase Chain ReactionSymbiosisBacterial ProteinsDNA Transposable Elementsbacterial colonizationbiofilmchaperonefunctional genomicssymbiosis

Identifiers

PMID25404340
PMCPMC4260577

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.