Evidence map›Paper›PMID 29718271›Full record

ReviewPathogens and disease2018

Cholesterol and fatty acids grease the wheels of Mycobacterium tuberculosis pathogenesis.

Kaley M Wilburn, Rachael A Fieweger, Brian C VanderVen

Abstract readReview
In one paragraph

Review in Pathogens and disease, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 101 papers.

0numbers the graph read from it
0cells of the map it votes in
101citing papers in PubMed
–field-weighted citation impact
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

101 citing papers in PubMed.

  1. Article
  2. Mce transport systems inJournal of bacteriology · 2026
    Review
  3. Article
  4. Article
  5. Impact of Diabetes Mellitus in Tuberculosis (TB) Patients on TB Transmission.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2026
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. ThemBio · 2026
    Article
  11. Article
  12. Clonal spread of Mycobacterium monacense strains among patients with extrapulmonary mycobacteriosis.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2026
    Article
  13. Review
  14. Whole Genome Sequencing of ClinicalInternational journal of molecular sciences · 2025
    Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Metabolic rewiring of isoniazid sensitivity inProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  20. Article

41 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

3 authors.

Kaley M WilburnDepartment of Microbiology and Immunology, College of Veterinary Medicine, Cornell University, Ithaca, New York 14850, USA.
Rachael A FiewegerDepartment of Microbiology and Immunology, College of Veterinary Medicine, Cornell University, Ithaca, New York 14850, USA.
Brian C VanderVenDepartment of Microbiology and Immunology, College of Veterinary Medicine, Cornell University, Ithaca, New York 14850, USA.

Funding

Preclinical evaluation of compounds that inhibit cholesterol uptake in M. tuberculosis.R01AI130018 · NIAID · CORNELL UNIVERSITY · PI VANDERVEN, BRIAN C · 2017 to 2021
$2.3M
Exploiting metabolic toxicities to identify compounds that inhibit cholesterol metabolism in M. TuberculosisR01AI119122 · NIAID · CORNELL UNIVERSITY · PI VANDERVEN, BRIAN C · 2015 to 2017
$1.2M
NIAID NIH HHS R01 AI119122NIAID NIH HHS R01 AI130018NIH HHS AI119122NIH HHS AI130018
6 · The paper itself

Abstract

Tuberculosis is a distinctive disease in which the causative agent, Mycobacterium tuberculosis, can persist in humans for decades by avoiding clearance from host immunity. During infection, M. tuberculosis maintains viability by extracting and utilizing essential nutrients from the host, and this is a prerequisite for all of the pathogenic activities that are deployed by the bacterium. In particular, M. tuberculosis preferentially acquires and metabolizes host-derived lipids (fatty acids and cholesterol), and the bacterium utilizes these substrates to cause and maintain disease. In this review, we discuss our current understanding of lipid utilization by M. tuberculosis, and we describe how these pathways promote pathogenesis to fuel metabolic processes in the bacillus. Finally, we highlight weaknesses in these pathways that potentially can be targeted for drug discovery.

Indexed as

AnimalsCholesterolFatty AcidsHumansMycobacterium tuberculosisTuberculosisCholesterolFatty Acids

Identifiers

PMID29718271
PMCPMC6251666

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.