Evidence map›Paper›PMID 23646936›Full record

ArticleMolecular microbiology2013

Conflicting roles for a cell surface modification in Salmonella.

John F May, Eduardo A Groisman

Open access · bronzeAbstract read
In one paragraph

Article in Molecular microbiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.8field-weighted citation impact, top 35% 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

13 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Changes in the genomes and methylomes of threeFrontiers in microbiology · 2022
    Article
  5. Article
  6. Article
  7. Evidence for Involvement of theFrontiers in microbiology · 2021
    Article
  8. LpxT-Dependent Phosphorylation of Lipid A inFrontiers in microbiology · 2021
    Article
  9. Article
  10. Article
  11. The Transcription Factor ArcA ModulatesFrontiers in microbiology · 2019
    Article
  12. Article
  13. 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

2 authors at 2 institutions in 1 country.

John F MayDepartment of Microbial Pathogenesis, Yale School of Medicine, New Haven, CT 06536, USA.
Eduardo A Groisman
Howard Hughes Medical Institute · USYale University · US

Funding

MOLECULAR AND STRUCTURAL BASES OF POLYMYXIN RESISTANCER01AI042236 · NIAID · YALE UNIVERSITY · PI GROISMAN, EDUARDO · 1998 to 2013
$3.0M
Co-opting ancestral regulatory systems to control bacterial virulenceR56AI042236 · NIAID · YALE UNIVERSITY · PI GROISMAN, EDUARDO · 2015 to 2015
$368k
Physiological roles of regulated changes in membrane phospholipid compositionF32GM097955 · NIGMS · YALE UNIVERSITY · PI MAY, JOHN · 2011 to 2012
$101k
Howard Hughes Medical InstituteNIAID NIH HHS AI042236NIAID NIH HHS R01 AI042236NIAID NIH HHS R56 AI042236NIGMS NIH HHS F32 GM097955NIGMS NIH HHS F32GM097955
6 · The paper itself

Abstract

Chemical modifications of components of the bacterial cell envelope can enhance resistance to antimicrobial agents. Why then are such modifications produced only under specific conditions? Here, we address this question by examining the role of regulated variations in O-antigen length in the lipopolysaccharide (LPS), a glycolipid that forms most of the outer leaflet of the outer membrane in Gram-negative bacteria. We determined that activation of the PmrA/PmrB two-component system, which is the major regulator of LPS alterations in Salmonella enterica serovar Typhimurium, impaired growth of Salmonella in bile. This growth defect required the PmrA-activated gene wzz(st), which encodes the protein that determines long O-antigen chain length and confers resistance to complement-mediated killing. By contrast, this growth defect did not require the wzz(fepE) gene, which controls production of very long O-antigen, or other PmrA-activated genes that mediate modifications of lipid A or core regions of the LPS. Additionally, we establish that long O-antigen inhibits growth in bile only in the presence of enterobacterial common antigen, an outer-membrane glycolipid that contributes to bile resistance. Our results suggest that Salmonella regulates the proportion of long O-antigen in its LPS to respond to the different conditions it faces during infection.

Indexed as

Bacterial ProteinsBileGene Expression Regulation, BacterialO AntigensSalmonella typhimuriumStress, PhysiologicalBacterial ProteinsO AntigenspmrA protein, Bacteriarol protein, Bacteria

Identifiers

PMID23646936
PMCPMC4081025
OpenAlexW1712202213

What OpenQuestion holds

Textmetadata
LicenceTDM
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.