Evidence map›Paper›PMID 23028312›Full record

ArticlePLoS pathogens2012

The Legionella IcmSW complex directly interacts with DotL to mediate translocation of adaptor-dependent substrates.

Molly C Sutherland, Thuy Linh Nguyen, Victor Tseng, Joseph P Vogel

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing 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

39 citing papers in PubMed, 68 citations in OpenAlex.

  1. Article
  2. Review
  3. Molecular evolution and adaptations ofFrontiers in cellular and infection microbiology · 2026
    Review
  4. Journal of bacteriology · 2024
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  5. Article
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  7. Membrane association and polar localization of theProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Structural basis for effector recognition by an antibacterial type IV secretion system.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  13. Review
  14. Review
  15. Major Outer Membrane Protein fromJournal of immunology research · 2021
    Article
  16. Review
  17. Dependency ofJournal of bacteriology · 2019
    Article
  18. Article
  19. Review
  20. Delivery of theFrontiers in microbiology · 2019
    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

4 authors at 2 institutions in 1 country.

Molly C SutherlandDepartment of Molecular Microbiology, Washington University School of Medicine, St. Louis, Missouri, USA.
Thuy Linh Nguyen
Victor Tseng
Joseph P Vogel
Washington University in St. Louis · USNew York Medical College · US

Funding

The molecular mechanism of Legionella type IV secretionR01AI048052 · NIAID · WASHINGTON UNIVERSITY · PI VOGEL, JOSEPH P · 2001 to 2010
$2.7M
NIAID NIH HHS AI48052NIAID NIH HHS R01 AI048052
6 · The paper itself

Abstract

Legionella pneumophila is a Gram-negative bacterium that replicates within human alveolar macrophages by evasion of the host endocytic pathway through the formation of a replicative vacuole. Generation of this vacuole is dependent upon the secretion of over 275 effector proteins into the host cell via the Dot/Icm type IVB secretion system (T4SS). The type IV coupling protein (T4CP) subcomplex, consisting of DotL, DotM, DotN, IcmS and IcmW, was recently defined. DotL is proposed to be the T4CP of the L. pneumophila T4SS based on its homology to known T4CPs, which function as inner-membrane receptors for substrates. As a result, DotL is hypothesized to play an integral role(s) in the L. pneumophila T4SS for the engagement and translocation of substrates. To elucidate this role, a genetic approach was taken to screen for dotL mutants that were unable to survive inside host cells. One mutant, dotLY725Stop, did not interact with the type IV adaptor proteins IcmS/IcmW (IcmSW) leading to the identification of an IcmSW-binding domain on DotL. Interestingly, the dotLY725Stop mutant was competent for export of one class of secreted effectors, the IcmSW-independent substrates, but exhibited a specific defect in secretion of IcmSW-dependent substrates. This differential secretion illustrates that DotL requires a direct interaction with the type IV adaptor proteins for the secretion of a major class of substrates. Thus, by identifying a new target for IcmSW, we have discovered that the type IV adaptors perform an additional role in the export of substrates by the L. pneumophila Dot/Icm T4SS.

Indexed as

Bacterial Secretion SystemsAcanthamoeba castellaniiBacterial ProteinsBinding SitesGene Expression Regulation, BacterialHumansLegionella pneumophilaMacrophagesMolecular ChaperonesMutationProtein BindingProtein TransportBacterial ProteinsBacterial Secretion SystemsDotL protein, Legionella pneumophilaIcmS protein, Legionella pneumophilaMolecular Chaperones

Identifiers

PMID23028312
PMCPMC3441705
OpenAlexW2123635061

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.