Evidence map›Paper›PMID 20975946›Full record

ArticlePLoS pathogens2010

Mycobacterium leprae phenolglycolipid-1 expressed by engineered M. bovis BCG modulates early interaction with human phagocytes.

Guillaume Tabouret, Catherine Astarie-Dequeker, Caroline Demangel, Wladimir Malaga, Patricia Constant, Aurélie Ray, Nadine Honoré, Nana Fatimath Bello, Esther Perez, Mamadou Daffé and 1 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.3field-weighted citation impact, top 13% 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, 90 citations in OpenAlex.

  1. Article
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  8. Modulation of the Response toFrontiers in microbiology · 2022
    Review
  9. Review
  10. Review
  11. Phthiocerol Dimycocerosates FromFrontiers in cellular and infection microbiology · 2020
    Article
  12. Trafficking ofFrontiers in immunology · 2020
    Review
  13. Underestimated Manipulative Roles ofFrontiers in immunology · 2019
    Review
  14. Article
  15. Article
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  17. 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

11 authors at 5 institutions in 1 country.

Guillaume TabouretCNRS, IPBS (Institut de Pharmacologie et de Biologie Structurale), Toulouse, France.
Catherine Astarie-Dequeker
Caroline Demangel
Wladimir Malaga
Patricia Constant
Aurélie Ray
Nadine Honoré
Nana Fatimath Bello
Esther Perez
Mamadou Daffé
Christophe Guilhot
Université Fédérale de Toulouse Midi-Pyrénées · FRCentre National de la Recherche Scientifique · FRInstitut de Pharmacologie et de Biologie Structurale · FRInstitut Pasteur · FRUniversité Toulouse III - Paul Sabatier · FR

Funding

Leprosy Research Support-Post Genome -26625469N01AI025469 · NIAID · Colorado State University · 2004 to 2004
–
NIAID NIH HHS N01 AI025469
6 · The paper itself

Abstract

The species-specific phenolic glycolipid 1 (PGL-1) is suspected to play a critical role in the pathogenesis of leprosy, a chronic disease of the skin and peripheral nerves caused by Mycobacterium leprae. Based on studies using the purified compound, PGL-1 was proposed to mediate the tropism of M. leprae for the nervous system and to modulate host immune responses. However, deciphering the biological function of this glycolipid has been hampered by the inability to grow M. leprae in vitro and to genetically engineer this bacterium. Here, we identified the M. leprae genes required for the biosynthesis of the species-specific saccharidic domain of PGL-1 and reprogrammed seven enzymatic steps in M. bovis BCG to make it synthesize and display PGL-1 in the context of an M. leprae-like cell envelope. This recombinant strain provides us with a unique tool to address the key questions of the contribution of PGL-1 in the infection process and to study the underlying molecular mechanisms. We found that PGL-1 production endowed recombinant BCG with an increased capacity to exploit complement receptor 3 (CR3) for efficient invasion of human macrophages and evasion of inflammatory responses. PGL-1 production also promoted bacterial uptake by human dendritic cells and dampened their infection-induced maturation. Our results therefore suggest that M. leprae produces PGL-1 for immune-silent invasion of host phagocytic cells.

Indexed as

AnimalsAntigen PresentationAntigens, BacterialCells, CulturedCHO CellsCricetinaeCricetulusGlycolipidsHumansImmune EvasionImmunity, InnateModels, BiologicalMycobacterium bovisMycobacterium lepraePhagocytesProtein EngineeringAntigens, BacterialGlycolipidsphenolic glycolipid I, Mycobacterium lepraeRecombinant Proteins

Identifiers

PMID20975946
PMCPMC2958813
OpenAlexW2017756984

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.