Evidence map›Paper›PMID 16997951›Full record

ArticleJournal of bacteriology2006

Identification of non-dot/icm suppressors of the Legionella pneumophila DeltadotL lethality phenotype.

Carr D Vincent, Benjamin A Buscher, Jonathan R Friedman, Lee Anne Williams, Patrick Bardill, Joseph P Vogel

Open access · greenAbstract read
In one paragraph

Article in Journal of bacteriology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

18 citing papers in PubMed, 28 citations in OpenAlex.

  1. Membrane association and polar localization of theProceedings of the National Academy of Sciences of the United States of America · 2024
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  9. Advances in gastric cancer prevention.World journal of clinical oncology · 2012
    Article
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  13. Minimization of the Legionella pneumophila genome reveals chromosomal regions involved in host range expansion.Proceedings of the National Academy of Sciences of the United States of America · 2011
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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

6 authors at 2 institutions in 1 country.

Carr D VincentDepartment of Molecular Microbiology, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
Benjamin A Buscher
Jonathan R Friedman
Lee Anne Williams
Patrick Bardill
Joseph P Vogel
Apath (United States) · USWashington University in St. Louis · 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, a causative agent of bacterial pneumonia, survives inside phagocytic cells by avoiding rapid targeting to the lysosome. This bacterium utilizes a type IVB secretion system, encoded by the dot/icm genes, to replicate inside host cells. DotL, a critical component of the Dot/Icm secretion apparatus, functions as the type IV coupling protein. In contrast to most dot/icm genes, which are dispensable for growth on bacteriological media, dotL is required for the viability of wild-type L. pneumophila. Previously we reported that DeltadotL lethality could be suppressed by inactivation of the Dot/Icm complex via mutations in other dot/icm genes. Here we report the isolation of non-dot/icm suppressors of this phenotype. These DeltadotL suppressors include insertions that disrupt the function of the L. pneumophila homologs of cpxR, djlA, lysS, and two novel open reading frames, lpg0742 and lpg1594, that we have named ldsA and ldsB for lethality of DeltadotL suppressor. In addition to suppressing DeltadotL lethality, inactivation of these genes in a wild-type strain background causes a range of defects in L. pneumophila virulence traits, including intracellular growth, implicating these factors in the proper function of the Dot/Icm complex. Consistent with previous data showing a role for the cpx system in regulating expression of several dot/icm genes, the cpxR insertion mutant produced decreased levels of three Dot/Icm proteins, DotA, IcmV, and IcmW. The remaining four suppressors did not affect the steady-state levels of any Dot/Icm protein and are likely to represent the first identified factors necessary for assembly and/or activation of the Dot/Icm secretion complex.

Indexed as

Genes, BacterialMultigene FamilySuppression, GeneticAnimalsBacterial ProteinsCarrier ProteinsGenes, SuppressorHSP40 Heat-Shock ProteinsHumansLegionella pneumophilaLegionnaires' DiseaseMacrophagesMembrane ProteinsMiceMolecular ChaperonesOpen Reading FramesBacterial ProteinsCarrier ProteinsCpxR protein, BacteriaDotA protein, Legionella pneumophilaDotL protein, Legionella pneumophilaHSP40 Heat-Shock ProteinsMembrane ProteinsMolecular Chaperones

Identifiers

PMID16997951
PMCPMC1698199
OpenAlexW2108662926

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.