Evidence map›Paper›PMID 24037657›Full record

ArticleJournal of microbiology (Seoul, Korea)2013

Free mycolic acid accumulation in the cell wall of the mce1 operon mutant strain of Mycobacterium tuberculosis.

Sally A Cantrell, Michael D Leavell, Olivera Marjanovic, Anthony T Iavarone, Julie A Leary, Lee W Riley

Abstract read
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In one paragraph

Article in Journal of microbiology (Seoul, Korea), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 12% 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

36 citing papers in PubMed, 1 synthesis or guideline pooled it, 71 citations in OpenAlex.

  1. Pooled it
  2. Mce transport systems inJournal of bacteriology · 2026
    Review
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  5. Antibiotic resistance inJAC-antimicrobial resistance · 2024
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  6. Article
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  8. Article
  9. Article
  10. Genomic analysis ofFrontiers in microbiology · 2022
    Article
  11. ATP disrupts lipid-binding equilibrium to drive retrograde transport critical for bacterial outer membrane asymmetry.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  12. Cell surface (Amsterdam, Netherlands) · 2021
    Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. High-Throughput Screen for Cell Wall Synthesis Network Module inFrontiers in bioengineering and biotechnology · 2020
    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 1 country.

Sally A CantrellDivision of Infectious Diseases and Vaccinology, School of Public Health, University of California, Berkeley, 94720, USA.
Michael D Leavell
Olivera Marjanovic
Anthony T Iavarone
Julie A Leary
Lee W Riley
University of California System · USUniversity of California, Berkeley · US

Funding

In vivo regulation of M. tuberculosis cell wall lipidsR01AI073204 · NIAID · UNIVERSITY OF CALIFORNIA BERKELEY · PI RILEY, LEE W · 2009 to 2010
$739k
NIAID NIH HHS R01AI073204
6 · The paper itself

Abstract

The lipid-rich cell wall of Mycobacterium tuberculosis, the agent of tuberculosis, serves as an effective barrier against many chemotherapeutic agents and toxic host cell effector molecules, and it may contribute to the mechanism of persistence. Mycobacterium tuberculosis strains mutated in a 13-gene operon called mce1, which encodes a putative ABC lipid transporter, induce aberrant granulomatous response in mouse lungs. Because of the postulated role of the mce1 operon in lipid importation, we compared the cell wall lipid composition of wild type and mce1 operon mutant M. tuberculosis H37Rv strains. High resolution mass spectrometric analyses of the mce1 mutant lipid extracts showed unbound mycolic acids to accumulate in the cell wall. Quantitative analysis revealed a 10.7 fold greater amount of free mycolates in the mutant compared to that of the wild type strain. The free mycolates were comprised of alpha, methoxy and keto mycolates in the ratio 1:0.9:0.6, respectively. Since the mce1 operon is regulated in vivo, the free mycolates that accumulate during infection may serve as a barrier for M. tuberculosis against toxic products and contribute to the pathogen's persistence.

Indexed as

MutationOperonBacterial ProteinsCell WallMass SpectrometryMycobacterium tuberculosisMycolic AcidsBacterial ProteinsMycolic Acids

Identifiers

PMID24037657
OpenAlexW2013580824

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.