Evidence map›Paper›PMID 16988222›Full record

ArticleInfection and immunity2006

The mgtC gene of Burkholderia cenocepacia is required for growth under magnesium limitation conditions and intracellular survival in macrophages.

Kendra E Maloney, Miguel A Valvano

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
4.5field-weighted citation impact, top 6% 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

38 citing papers in PubMed, 67 citations in OpenAlex.

  1. Article
  2. AliC and AliD of nonencapsulatedFrontiers in cellular and infection microbiology · 2025
    Article
  3. Impact of MgtC on the Fitness ofPathogens (Basel, Switzerland) · 2023
    Article
  4. Article
  5. Virulence Mechanisms ofFrontiers in microbiology · 2022
    Review
  6. How the PhoP/PhoQ System Controls Virulence and MgMicrobiology and molecular biology reviews : MMBR · 2021
    Review
  7. Review
  8. Article
  9. Article
  10. Activity of a Synthetic Peptide Targeting MgtC onFrontiers in cellular and infection microbiology · 2019
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Regulation and function of the Salmonella MgtC virulence protein.Journal of microbiology (Seoul, Korea) · 2015
    Review
  16. When Too Much ATP Is Bad for Protein Synthesis.Journal of molecular biology · 2015
    Review
  17. Article
  18. Salmonella promotes virulence by repressing cellulose production.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Article
  19. Control of a Salmonella virulence operon by proline-charged tRNA(Pro).Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  20. 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 2 countries.

Kendra E MaloneyInfectious Diseases Research Group, Siebens-Drake Research Institute, Department of Microbiology and Immunology, University of Western Ontario, London, Ontario, N6A 5C1, Canada.
Miguel A Valvano
Drake University · USWestern University · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Burkholderia cenocepacia, a bacterium commonly found in the environment, is an important opportunistic pathogen in patients with cystic fibrosis (CF). Very little is known about the mechanisms by which B. cenocepacia causes disease, but chronic infection of the airways in CF patients may be associated, at least in part, with the ability of this bacterium to survive within epithelial cells and macrophages. Survival in macrophages occurs in a membrane-bound compartment that is distinct from the lysosome, suggesting that B. cenocepacia prevents phagolysosomal fusion. In a previous study, we employed signature-tagged mutagenesis and an agar bead model of chronic pulmonary infection in rats to identify B. cenocepacia genes that are required for bacterial survival in vivo. One of the most significantly attenuated mutants had an insertion in the mgtC gene. Here, we show that mgtC is also needed for growth of B. cenocepacia in magnesium-depleted medium and for bacterial survival within murine macrophages. Using fluorescence microscopy, we demonstrated that B. cenocepacia mgtC mutants, unlike the parental isolate, colocalize with the fluorescent acidotropic probe LysoTracker Red. At 4 h postinfection, mgtC mutants expressing monomeric red fluorescent protein cannot retain this protein within the bacterial cytoplasm. Together, these results demonstrate that, unlike the parental strain, an mgtC mutant does not induce a delay in phagolysosomal fusion and the bacterium-containing vacuoles are rapidly targeted to the lysosome, where bacteria are destroyed.

Indexed as

Genes, BacterialAnimalsBacterial ProteinsBurkholderia cepacia complexCation Transport ProteinsCell LineDNA Transposable ElementsMacrophagesMagnesiumMiceMutagenesis, InsertionalMutationReactive Nitrogen SpeciesReactive Oxygen SpeciesBacterial ProteinsCation Transport ProteinsDNA Transposable ElementsMagnesiumReactive Nitrogen SpeciesReactive Oxygen Species

Identifiers

PMID16988222
PMCPMC1594880
OpenAlexW2017056768

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.