Evidence map›Paper›PMID 25987704›Full record

ArticleInfection and immunity2015

Identifying Francisella tularensis genes required for growth in host cells.

J Brunton, S Steele, C Miller, E Lovullo, S Taft-Benz, T Kawula

Open access · bronzeAbstract read
In one paragraph

Article in Infection and immunity, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

9 citing papers in PubMed, 11 citations in OpenAlex.

  1. Functional characterization ofFrontiers in cellular and infection microbiology · 2024
    Article
  2. Article
  3. Peptidoglycan enzymes ofFrontiers in microbiology · 2022
    Review
  4. Article
  5. Article
  6. AFrontiers in microbiology · 2019
    Article
  7. Article
  8. Article
  9. 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

6 authors at 3 institutions in 1 country.

J BruntonDepartment of Microbiology and Immunology, School of Medicine, University of North Carolina, Chapel Hill, North Carolina, USA.
S SteeleDepartment of Microbiology and Immunology, School of Medicine, University of North Carolina, Chapel Hill, North Carolina, USA.
C MillerPaul G. Allen School for Global Animal Health, College of Veterinary Medicine, Washington State University, Pullman, Washington, USA.
E LovulloCenter for Medical, Agricultural, and Veterinary Entomology, Agricultural Research Service, U.S. Department of Agriculture, Gainesville, Florida, USA.
S Taft-BenzDepartment of Microbiology and Immunology, School of Medicine, University of North Carolina, Chapel Hill, North Carolina, USA.
T KawulaDepartment of Microbiology and Immunology, School of Medicine, University of North Carolina, Chapel Hill, North Carolina, USA kawula@med.unc.edu.
University of North Carolina at Chapel Hill · USCenter for Medical, Agricultural and Veterinary Entomology · USWashington State University · US

Funding

Francisella tularensis PathogenesisR01AI082870 · NIAID · WASHINGTON STATE UNIVERSITY · PI KAWULA, THOMAS H · 2010 to 2019
$3.2M
Francisella tularensis PathogenesisR56AI082870 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI KAWULA, THOMAS H · 2009 to 2010
$402k
NIAID NIH HHS AI082870NIAID NIH HHS R01 AI082870NIAID NIH HHS R56 AI082870
6 · The paper itself

Abstract

Francisella tularensis is a highly virulent Gram-negative intracellular pathogen capable of infecting a vast diversity of hosts, ranging from amoebae to humans. A hallmark of F. tularensis virulence is its ability to quickly grow to high densities within a diverse set of host cells, including, but not limited to, macrophages and epithelial cells. We developed a luminescence reporter system to facilitate a large-scale transposon mutagenesis screen to identify genes required for growth in macrophage and epithelial cell lines. We screened 7,454 individual mutants, 269 of which exhibited reduced intracellular growth. Transposon insertions in the 269 growth-defective strains mapped to 68 different genes. FTT_0924, a gene of unknown function but highly conserved among Francisella species, was identified in this screen to be defective for intracellular growth within both macrophage and epithelial cell lines. FTT_0924 was required for full Schu S4 virulence in a murine pulmonary infection model. The ΔFTT_0924 mutant bacterial membrane is permeable when replicating in hypotonic solution and within macrophages, resulting in strongly reduced viability. The permeability and reduced viability were rescued when the mutant was grown in a hypertonic solution, indicating that FTT_0924 is required for resisting osmotic stress. The ΔFTT_0924 mutant was also significantly more sensitive to β-lactam antibiotics than Schu S4. Taken together, the data strongly suggest that FTT_0924 is required for maintaining peptidoglycan integrity and virulence.

Indexed as

AnimalsBacterial ProteinsCell LineFrancisella tularensisGenes, ReporterHumansMacrophagesMaleMiceMice, Inbred C57BLMutagenesis, InsertionalTularemiaVirulenceBacterial Proteins

Identifiers

PMID25987704
PMCPMC4496600
OpenAlexW2165704089

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.