Evidence map›Paper›PMID 16436697›Full record

ArticleAntimicrobial agents and chemotherapy2006

The two-component regulatory system mtrAB is required for morphotypic multidrug resistance in Mycobacterium avium.

Gerard A Cangelosi, Julie S Do, Robert Freeman, John G Bennett, Makeda Semret, Marcel A Behr

Open access · greenAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2006. 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
3.8field-weighted citation impact, top 7% 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, 80 citations in OpenAlex.

  1. Cell wall remodeling-dependent morphotype switch inProceedings of the National Academy of Sciences of the United States of America · 2026
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  2. Tamoxifen inhibits histidine kinases ofMicrobiology spectrum · 2026
    Article
  3. Unusual Genomic and Biochemical Features ofInternational journal of molecular sciences · 2024
    Article
  4. Regulatory role ofFrontiers in microbiology · 2024
    Article
  5. Article
  6. Article
  7. Variability ofAntibiotics (Basel, Switzerland) · 2022
    Review
  8. Article
  9. Review
  10. Review
  11. The sensor kinase MtrB ofThe Journal of biological chemistry · 2019
    Article
  12. Review
  13. Review
  14. Cloning and characterization ofMolecular biology research communications · 2018
    Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Mycobacterial Growth.Cold Spring Harbor perspectives in medicine · 2015
    Review
  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

6 authors at 2 institutions in 2 countries.

Gerard A CangelosiSeattle Biomedical Research Institute, 307 Westlake Avenue N., Suite 500, Seattle, WA 98109, USA. Jerry.Cangelosi@sbri.org
Julie S Do
Robert Freeman
John G Bennett
Makeda Semret
Marcel A Behr
Center for Infectious Disease Research · USMcGill University Health Centre · CA

Funding

Genetic Analysis of Mycobacterial Biofilm FormationR21AI061006 · NIAID · SEATTLE BIOMEDICAL RESEARCH INSTITUTE · PI CANGELOSI, GERARD A · 2004 to 2005
$457k
NIAID NIH HHS R01-AI25767NIAID NIH HHS R21 AI061006NIAID NIH HHS R21-AI061006
6 · The paper itself

Abstract

Clinical isolates of the opportunistic pathogen Mycobacterium avium complex (MAC) undergo a reversible switch between red and white colony morphotypes on agar plates containing the lipoprotein stain Congo red. Compared to their isogenic red counterparts, white morphotypic variants are more virulent and more resistant to multiple antibiotics. This report shows that the two-component regulatory system mtrAB is required for the red-to-white switch as well as for other morphotypic switches of MAC. A mutant with a transposon insertion in the histidine protein kinase gene mtrB was isolated from a morphotypically white parent clone. The mutant resembled a naturally occurring red morphotypic variant in that it stained with Congo red, was sensitive to multiple antibiotics, and was permeable by a fluorescent DNA stain. However, it differed from a red variant in that it could not switch to the white or transparent morphotype, and it could not survive intracellularly within macrophage-like cells. Transcomplementation with a cloned wild-type mtrB gene restored to the mutant the ability to form impermeable, drug-resistant white and transparent variants. Quantitative reverse transcriptase PCR showed that mtrB was required for the normal expression of cell surface Mce proteins, some of which are up-regulated in the red-to-white switch. The results indicate that mtrAB functions in regulating the composition and permeability of mycobacterial cell walls and plays a role in the reversible colony type switches of MAC.

Indexed as

Drug Resistance, Multiple, BacterialATP-Binding Cassette TransportersBacterial ProteinsCell LineCell WallHumansMycobacterium avium ComplexPermeabilityRNA-Binding ProteinsTranscription FactorsATP-Binding Cassette TransportersBacterial ProteinsMtrA protein, BacteriaMtrB protein, BacteriaRNA-Binding ProteinsTranscription Factors

Identifiers

PMID16436697
PMCPMC1366905
OpenAlexW2018426941

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.