Evidence map›Paper›PMID 15231779›Full record

ArticleJournal of bacteriology2004

SadB is required for the transition from reversible to irreversible attachment during biofilm formation by Pseudomonas aeruginosa PA14.

Nicky C Caiazza, George A O'Toole

Abstract read
In one paragraph

Article in Journal of bacteriology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 104 papers.

0numbers the graph read from it
0cells of the map it votes in
104citing 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

104 citing papers in PubMed.

  1. Review
  2. Article
  3. ThemBio · 2026
    Article
  4. UnderstandingMicroorganisms · 2026
    Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Development of a tomato xylem-mimicking microfluidic system to studyFrontiers in bioengineering and biotechnology · 2024
    Article
  12. Review
  13. Swarming ofBiophysics reviews · 2023
    Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Review
  20. Article

44 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

2 authors.

Nicky C CaiazzaDepartment of Microbiology and Immunology, Dartmouth Medical School, Room 202, Vail Building, Hanover, NH 03755, USA.
George A O'Toole

Funding

Mechanisms of Biofilm Antibiotic ResistanceR01AI051360 · NIAID · DARTMOUTH COLLEGE · PI O'TOOLE, GEORGE A. · 2003 to 2007
$1.8M
NIAID NIH HHS 1 R01 AI051360-01A1NIAID NIH HHS R01 AI051360
6 · The paper itself

Abstract

Current models of biofilm formation by Pseudomonas aeruginosa propose that (i) planktonic cells become surface associated in a monolayer, (ii) surface-associated cells form microcolonies by clonal growth and/or aggregation, (iii) microcolonies transition to a mature biofilm comprised of exopolysaccharide-encased macrocolonies, and (iv) cells exit the mature biofilm and reenter the planktonic state. Here we report a new class of P. aeruginosa biofilm mutant that defines the transition from reversible to irreversible attachment and is thus required for monolayer formation. The transposon insertion carried by the sadB199 mutant was mapped to open reading frame PA5346 of P. aeruginosa PA14 and encodes a protein of unknown function. Complementation analysis and phage-mediated transduction demonstrated that the transposon insertion in PA5346 was the cause of the biofilm-defective phenotype. Examination of flow cell-grown biofilms showed that the sadB199 mutant could initiate surface attachment but failed to form microcolonies despite being proficient in both twitching and swimming motility. Closer examination of early attachment revealed an increased number of the sadB199 mutant cells arrested at reversible attachment, functionally defined as adherence via the cell pole. A positive correlation among biofilm formation, irreversible attachment, and SadB level was demonstrated, and furthermore, RpoN and FleR appear to negatively affect SadB levels. Fractionation studies showed that the SadB protein is localized to the cytoplasm, and with the use of GPS-linker scanning mutagenesis, the C-terminal portion of SadB was shown to be dispensable for function, whereas the two putative domains of unknown function and the linker region spanning these domains were required for function. We discuss the results presented here in the context of microbial development as it applies to biofilm formation.

Indexed as

Bacterial AdhesionDNA-Binding ProteinsGenes, BacterialBacterial ProteinsBiofilmsChromosome MappingCytoplasmDNA-Directed RNA PolymerasesDNA Transposable ElementsGene Expression Regulation, BacterialGenetic Complementation TestMutagenesis, InsertionalMutationOpen Reading FramesProtein Structure, TertiaryPseudomonas aeruginosaBacterial ProteinsDNA-Binding ProteinsDNA-Directed RNA PolymerasesDNA Transposable ElementsFleR protein, Pseudomonas aeruginosaRNA Polymerase Sigma 54Sigma FactorTranscription Factors

Identifiers

PMID15231779
PMCPMC438627

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.