Evidence map›Paper›PMID 26077160›Full record

ArticleMolecular microbiology2015

Deciphering the metabolic response of Mycobacterium tuberculosis to nitrogen stress.

Kerstin J Williams, Victoria A Jenkins, Geraint R Barton, William A Bryant, Nitya Krishnan, Brian D Robertson

Open access · hybridAbstract read
In one paragraph

Article in Molecular microbiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

23 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Microbial metabolism disrupts cytokine activity to impact host immune response.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  3. Article
  4. Orphan response regulator NnaR is critical for nitrate and nitrite assimilation inFrontiers in cellular and infection microbiology · 2024
    Article
  5. Article
  6. Structural insights into the transcription activation mechanism of the global regulator GlnR from actinobacteria.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Metabolic Switching ofJournal of bacteriology · 2020
    Article
  13. Role of Proline in Pathogen and Host Interactions.Antioxidants & redox signaling · 2019
    Review
  14. Article
  15. Article
  16. Article
  17. The Unexpected Essentiality ofFrontiers in microbiology · 2018
    Article
  18. Article
  19. 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

6 authors at 1 institution in 1 country.

Kerstin J WilliamsMRC Centre for Molecular Bacteriology and Infection, Department of Medicine, Imperial College London, London, SW7 2AZ, UK.
Victoria A JenkinsMRC Centre for Molecular Bacteriology and Infection, Department of Medicine, Imperial College London, London, SW7 2AZ, UK.
Geraint R BartonCentre for Integrative Systems Biology and Bioinformatics, Imperial College London, London, SW7 2AZ, UK.
William A BryantCentre for Integrative Systems Biology and Bioinformatics, Imperial College London, London, SW7 2AZ, UK.
Nitya KrishnanMRC Centre for Molecular Bacteriology and Infection, Department of Medicine, Imperial College London, London, SW7 2AZ, UK.
Brian D RobertsonMRC Centre for Molecular Bacteriology and Infection, Department of Medicine, Imperial College London, London, SW7 2AZ, UK.
Imperial College London · GB

Funding

Biotechnology and Biological Sciences Research Council BB/G020434/1Medical Research Council MR/J006874/1
6 · The paper itself

Abstract

A key component to the success of Mycobacterium tuberculosis as a pathogen is the ability to sense and adapt metabolically to the diverse range of conditions encountered in vivo, such as oxygen tension, environmental pH and nutrient availability. Although nitrogen is an essential nutrient for every organism, little is known about the genes and pathways responsible for nitrogen assimilation in M. tuberculosis. In this study we have used transcriptomics and chromatin immunoprecipitation and high-throughput sequencing to address this. In response to nitrogen starvation, a total of 185 genes were significantly differentially expressed (96 up-regulated and 89 down regulated; 5% genome) highlighting several significant areas of metabolic change during nitrogen limitation such as nitrate/nitrite metabolism, aspartate metabolism and changes in cell wall biosynthesis. We identify GlnR as a regulator involved in the nitrogen response, controlling the expression of at least 33 genes in response to nitrogen limitation. We identify a consensus GlnR binding site and relate its location to known transcriptional start sites. We also show that the GlnR response regulator plays a very different role in M. tuberculosis to that in non-pathogenic mycobacteria, controlling genes involved in nitric oxide detoxification and intracellular survival instead of genes involved in nitrogen scavenging.

Indexed as

Metabolic Networks and PathwaysAmmonium CompoundsAspartic AcidBacterial ProteinsBinding SitesCell WallChromatin ImmunoprecipitationGene Expression ProfilingGene Expression Regulation, BacterialMycobacterium tuberculosisNitrogenProtein BindingResponse ElementsStress, PhysiologicalAmmonium CompoundsAspartic AcidBacterial ProteinsNitrogen

Identifiers

PMID26077160
PMCPMC4950008
OpenAlexW2161399578

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.