Evidence map›Paper›PMID 26603639›Full record

ArticleScientific reports2015

Revisiting the role of phospholipases C in virulence and the lifecycle of Mycobacterium tuberculosis.

Fabien Le Chevalier, Alessandro Cascioferro, Wafa Frigui, Alexandre Pawlik, Eva C Boritsch, Daria Bottai, Laleh Majlessi, Jean Louis Herrmann, Roland Brosch

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing 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

28 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Roles of Lipolytic enzymes inFrontiers in microbiology · 2024
    Review
  7. Article
  8. Phospholipase C: underrated players in microbial infections.Frontiers in cellular and infection microbiology · 2023
    Review
  9. In Silico Exploration ofBiomolecules · 2022
    Article
  10. Article
  11. Article
  12. ISFrontiers in microbiology · 2022
    Article
  13. Functional Analysis of Hypothetical Proteins ofBioinformatics and biology insights · 2022
    Article
  14. Virulence Mechanisms ofFrontiers in microbiology · 2022
    Review
  15. Review
  16. Article
  17. Pathogenomic analyses ofMicrobial genomics · 2021
    Article
  18. Article
  19. Review
  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

9 authors at 3 institutions in 2 countries.

Fabien Le ChevalierInstitut Pasteur, Unit for Integrated Mycobacterial Pathogenomics, F-75015, Paris, France.
Alessandro CascioferroInstitut Pasteur, Unit for Integrated Mycobacterial Pathogenomics, F-75015, Paris, France.
Wafa FriguiInstitut Pasteur, Unit for Integrated Mycobacterial Pathogenomics, F-75015, Paris, France.
Alexandre PawlikInstitut Pasteur, Unit for Integrated Mycobacterial Pathogenomics, F-75015, Paris, France.
Eva C BoritschInstitut Pasteur, Unit for Integrated Mycobacterial Pathogenomics, F-75015, Paris, France.
Daria BottaiDipartimento di Ricerca Traslazionale e delle Nuove Tecnologie in Medicina e Chirurgia, University of Pisa, Italy.
Laleh MajlessiInstitut Pasteur, Unit for Integrated Mycobacterial Pathogenomics, F-75015, Paris, France.
Jean Louis HerrmannINSERM U1173, UFR Sciences de la Santé Simone Veil, Université Versailles-Saint-Quentin, 78180 Saint-Quentin en Yvelines, France.
Roland BroschInstitut Pasteur, Unit for Integrated Mycobacterial Pathogenomics, F-75015, Paris, France.
Institut Pasteur · FRInserm · FRUniversity of Pisa · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mycobacterium tuberculosis, the agent of human tuberculosis has developed different virulence mechanisms and virulence-associated tools during its evolution to survive and multiply inside the host. Based on previous reports and by analogy with other bacteria, phospholipases C (PLC) of M. tuberculosis were thought to be among these tools. To get deeper insights into the function of PLCs, we investigated their putative involvement in the intracellular lifestyle of M. tuberculosis, with emphasis on phagosomal rupture and virulence, thereby re-visiting a research theme of longstanding interest. Through the construction and use of an M. tuberculosis H37Rv PLC-null mutant (ΔPLC) and control strains, we found that PLCs of M. tuberculosis were not required for induction of phagosomal rupture and only showed marginal, if any, impact on virulence of M. tuberculosis in the cellular and mouse infection models used in this study. In contrast, we found that PLC-encoding genes were strongly upregulated under phosphate starvation and that PLC-proficient M. tuberculosis strains survived better than ΔPLC mutants under conditions where phosphatidylcholine served as sole phosphate source, opening new perspectives for studies on the role of PLCs in the lifecycle of M. tuberculosis.

Indexed as

AnimalsBacterial ProteinsCell LineColorimetryFemaleHumansLife Cycle StagesLungMacrophagesMiceMice, Inbred C57BLMice, SCIDMycobacterium tuberculosisOperonPhagosomesPhosphatidylcholinesBacterial ProteinsPhosphatidylcholinesType C Phospholipases

Identifiers

PMID26603639
PMCPMC4658479
OpenAlexW2408820431

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.