Evidence map›Paper›PMID 24552180›Full record

ArticleCellular microbiology2014

Mycobacterium leprae intracellular survival relies on cholesterol accumulation in infected macrophages: a potential target for new drugs for leprosy treatment.

Katherine A Mattos, Viviane C G Oliveira, Marcia Berrêdo-Pinho, Julio J Amaral, Luis Caetano M Antunes, Rossana C N Melo, Chyntia C D Acosta, Danielle F Moura, Roberta Olmo, Jun Han and 8 more

Open access · hybridAbstract read
In one paragraph

Article in Cellular microbiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

59 citing papers in PubMed, 88 citations in OpenAlex.

  1. Trial
  2. AMetabolites · 2026
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  3. Impact of protein prenylation inhibition onJournal of bacteriology · 2025
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  4. Article
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  6. IFN-γ-Driven macrophage responses in the immunity toFrontiers in cellular and infection microbiology · 2025
    Review
  7. Article
  8. Article
  9. Adenosine AFrontiers in pharmacology · 2024
    Article
  10. Review
  11. Article
  12. Review
  13. Bovine Immunity and Vitamin DMicroorganisms · 2022
    Review
  14. Article
  15. Modulation of the Response toFrontiers in microbiology · 2022
    Review
  16. Essential Roles of PPARs in Lipid Metabolism during Mycobacterial Infection.International journal of molecular sciences · 2021
    Review
  17. Article
  18. Review
  19. Review
  20. Reductive Power Generated byFrontiers in cellular and infection microbiology · 2021
    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

18 authors at 7 institutions in 2 countries.

Katherine A MattosLaboratório de Microbiologia Celular, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz, Rio de Janeiro, 21040-900, RJ, Brazil.
Viviane C G Oliveira
Marcia Berrêdo-Pinho
Julio J Amaral
Luis Caetano M Antunes
Rossana C N Melo
Chyntia C D Acosta
Danielle F Moura
Roberta Olmo
Jun Han
Patricia S Rosa
Patrícia E Almeida
B Brett Finlay
Christoph H Borchers
Euzenir N Sarno
Patricia T Bozza
Georgia C Atella
Maria Cristina V Pessolani
Fundação Oswaldo Cruz · BRUniversidade Federal de Juiz de Fora · BRUniversity of Victoria · CACanada's Michael Smith Genome Sciences Centre · CAInstituto Lauro de Souza Lima · BRUniversidade Federal do Rio de Janeiro · BRUniversity of British Columbia · CA

Funding

Canadian Institutes of Health Research
6 · The paper itself

Abstract

We recently showed that Mycobacterium leprae (ML) is able to induce lipid droplet formation in infected macrophages. We herein confirm that cholesterol (Cho) is one of the host lipid molecules that accumulate in ML-infected macrophages and investigate the effects of ML on cellular Cho metabolism responsible for its accumulation. The expression levels of LDL receptors (LDL-R, CD36, SRA-1, SR-B1, and LRP-1) and enzymes involved in Cho biosynthesis were investigated by qRT-PCR and/or Western blot and shown to be higher in lepromatous leprosy (LL) tissues when compared to borderline tuberculoid (BT) lesions. Moreover, higher levels of the active form of the sterol regulatory element-binding protein (SREBP) transcriptional factors, key regulators of the biosynthesis and uptake of cellular Cho, were found in LL skin biopsies. Functional in vitro assays confirmed the higher capacity of ML-infected macrophages to synthesize Cho and sequester exogenous LDL-Cho. Notably, Cho colocalized to ML-containing phagosomes, and Cho metabolism impairment, through either de novo synthesis inhibition by statins or depletion of exogenous Cho, decreased intracellular bacterial survival. These findings highlight the importance of metabolic integration between the host and bacteria to leprosy pathophysiology, opening new avenues for novel therapeutic strategies to leprosy.

Indexed as

Host-Pathogen InteractionsMicrobial ViabilityAnimalsBlotting, WesternCells, CulturedCholesterolGene Expression ProfilingHumansLeprosyMacrophagesMice, Inbred C57BLMycobacterium lepraePhagosomesReal-Time Polymerase Chain ReactionReceptors, LDLSterol Regulatory Element Binding ProteinsCholesterolReceptors, LDLSterol Regulatory Element Binding Proteins

Identifiers

PMID24552180
PMCPMC4262048
OpenAlexW1869447046

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.