Evidence map›Paper›PMID 31693670›Full record

ArticlePloS one2019

Lactobacillus rhamnosus Lcr35 as an effective treatment for preventing Candida albicans infection in the invertebrate model Caenorhabditis elegans: First mechanistic insights.

Cyril Poupet, Taous Saraoui, Philippe Veisseire, Muriel Bonnet, Caroline Dausset, Marylise Gachinat, Olivier Camarès, Christophe Chassard, Adrien Nivoliez, Stéphanie Bornes

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

22 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Metabolic Regulation of Longevity and Immune Response inJournal of microbiology and biotechnology · 2024
    Article
  7. Potential probiotic and functional properties ofFrontiers in microbiology · 2024
    Article
  8. Review
  9. A Potential ProbioticAntioxidants (Basel, Switzerland) · 2022
    Article
  10. Frontiers in nutrition · 2022
    Article
  11. Frontiers in microbiology · 2022
    Article
  12. Insights From theFrontiers in microbiology · 2022
    Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Frontiers in cellular and infection microbiology · 2021
    Review
  19. Article
  20. Frontiers in nutrition · 2020
    Review
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

10 authors at 1 institution in 1 country.

Cyril PoupetUniversité Clermont Auvergne, INRA, VetAgro Sup, Aurillac, France.ORCID 0000-0001-9343-4390
Taous SaraouiUniversité Clermont Auvergne, INRA, VetAgro Sup, Aurillac, France.
Philippe VeisseireUniversité Clermont Auvergne, INRA, VetAgro Sup, Aurillac, France.
Muriel BonnetUniversité Clermont Auvergne, INRA, VetAgro Sup, Aurillac, France.
Caroline DaussetBiose Industrie, Aurillac, France.ORCID 0000-0001-8281-1111
Marylise GachinatUniversité Clermont Auvergne, INRA, VetAgro Sup, Aurillac, France.
Olivier CamarèsUniversité Clermont Auvergne, INRA, VetAgro Sup, Aurillac, France.
Christophe ChassardUniversité Clermont Auvergne, INRA, VetAgro Sup, Aurillac, France.
Adrien NivoliezBiose Industrie, Aurillac, France.
Stéphanie BornesUniversité Clermont Auvergne, INRA, VetAgro Sup, Aurillac, France.
Université Clermont Auvergne · FR

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Aric L Daul, Ann E. Rougvie · 2012 to 2026
$7.5M
NIH HHS P40 OD010440
6 · The paper itself

Abstract

The increased recurrence of Candida albicans infections is associated with greater resistance to antifungal drugs. This involves the establishment of alternative therapeutic protocols, such as probiotic microorganisms whose antifungal potential has already been demonstrated using preclinical models (cell cultures, laboratory animals). Understanding the mechanisms of action of probiotic microorganisms has become a strategic need for the development of new therapeutics for humans. In this study, we investigated the prophylactic anti-C. albicans properties of Lactobacillus rhamnosus Lcr35® using the in vitro Caco-2 cell model and the in vivo Caenorhabditis elegans model. In Caco-2 cells, we showed that the strain Lcr35® significantly inhibited the growth (~2 log CFU.mL-1) and adhesion (150 to 6,300 times less) of the pathogen. Moreover, in addition to having a pro-longevity activity in the nematode (+42.9%, p = 3.56.10-6), Lcr35® protects the animal from the fungal infection (+267% of survival, p < 2.10-16) even if the yeast is still detectable in its intestine. At the mechanistic level, we noticed the repression of genes of the p38 MAPK signalling pathway and genes involved in the antifungal response induced by Lcr35®, suggesting that the pathogen no longer appears to be detected by the worm immune system. However, the DAF-16/FOXO transcription factor, implicated in the longevity and antipathogenic response of C. elegans, is activated by Lcr35®. These results suggest that the probiotic strain acts by stimulating its host via DAF-16 but also by suppressing the virulence of the pathogen.

Indexed as

Candida albicansLacticaseibacillus rhamnosusActive Transport, Cell NucleusAnimalsAnimals, Genetically ModifiedCaco-2 CellsCaenorhabditis elegansCaenorhabditis elegans ProteinsCandidiasisDisease Models, AnimalForkhead Transcription FactorsHost Microbial InteractionsHumansProbioticsVirulenceCaenorhabditis elegans Proteinsdaf-16 protein, C elegansForkhead Transcription Factors

Identifiers

PMID31693670
PMCPMC6834333
OpenAlexW2985101570

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.