Evidence map›Paper›PMID 21980288›Full record

ArticlePLoS pathogens2011

Evaluating the sensitivity of Mycobacterium tuberculosis to biotin deprivation using regulated gene expression.

Sae Woong Park, Marcus Klotzsche, Daniel J Wilson, Helena I Boshoff, Hyungjin Eoh, Ujjini Manjunatha, Antje Blumenthal, Kyu Rhee, Clifton E Barry, Courtney C Aldrich and 2 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 93 papers.

0numbers the graph read from it
0cells of the map it votes in
93citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

93 citing papers in PubMed, 142 citations in OpenAlex.

  1. CRISPRi-mediatedAntimicrobial agents and chemotherapy · 2026
    Article
  2. Article
  3. Review
  4. Exploring the Link Between Biotin Metabolism andPathogens (Basel, Switzerland) · 2026
    Article
  5. Article
  6. CRISPRi-mediated validation of candidatebioRxiv : the preprint server for biology · 2025
    Article
  7. Article
  8. Article
  9. Article
  10. New Potent Sulfonamide-Based Inhibitors ofACS medicinal chemistry letters · 2024
    Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Identification of essential genes inMicrobial genomics · 2023
    Article
  17. Article
  18. Article
  19. Review
  20. Article

33 more citing papers are in PubMed but not listed here.

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

12 authors at 5 institutions in 3 countries.

Sae Woong ParkDepartment of Microbiology and Immunology, Weill Cornell Medical College, New York, New York, United States of America.
Marcus Klotzsche
Daniel J Wilson
Helena I Boshoff
Hyungjin Eoh
Ujjini Manjunatha
Antje Blumenthal
Kyu Rhee
Clifton E Barry
Courtney C Aldrich
Sabine Ehrt
Dirk Schnappinger
Cornell University · USNational Institute of Allergy and Infectious Diseases · USCenter for Drug Evaluation and Research · USInstitute of Medicinal Plant Development · CNNovartis (Singapore) · SG

Funding

Exploring the metabolism of non-replicating and drug-resistant TBZIAAI000783 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI BARRY, CLIFTON · 2009 to 2017
$8.2M
Conditional Expression of Mycobacterial GenesR01AI063446 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI EHRT, SABINE · 2006 to 2022
$7.2M
Intramural NIH HHSNIAID NIH HHS AI063446NIAID NIH HHS AI09179NIAID NIH HHS R01 AI063446Wellcome Trust
6 · The paper itself

Abstract

In the search for new drug targets, we evaluated the biotin synthetic pathway of Mycobacterium tuberculosis (Mtb) and constructed an Mtb mutant lacking the biotin biosynthetic enzyme 7,8-diaminopelargonic acid synthase, BioA. In biotin-free synthetic media, ΔbioA did not produce wild-type levels of biotinylated proteins, and therefore did not grow and lost viability. ΔbioA was also unable to establish infection in mice. Conditionally-regulated knockdown strains of Mtb similarly exhibited impaired bacterial growth and viability in vitro and in mice, irrespective of the timing of transcriptional silencing. Biochemical studies further showed that BioA activity has to be reduced by approximately 99% to prevent growth. These studies thus establish that de novo biotin synthesis is essential for Mtb to establish and maintain a chronic infection in a murine model of TB. Moreover, these studies provide an experimental strategy to systematically rank the in vivo value of potential drug targets in Mtb and other pathogens.

Indexed as

MutationAnimalsBacterial ProteinsBiotinChronic DiseaseDisease Models, AnimalDrug Delivery SystemsMiceMycobacterium tuberculosisTransaminasesTuberculosisBacterial ProteinsBioA protein, bacteriaBiotinTransaminases

Identifiers

PMID21980288
PMCPMC3182931
OpenAlexW2078355424

What OpenQuestion holds

Textmetadata
LicenceCC0
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.