Evidence map›Paper›PMID 33045003›Full record

ArticlePLoS pathogens2020

Fluorescent secreted bacterial effectors reveal active intravacuolar proliferation of Listeria monocytogenes in epithelial cells.

Caroline Peron-Cane, José-Carlos Fernandez, Julien Leblanc, Laure Wingertsmann, Arnaud Gautier, Nicolas Desprat, Alice Lebreton

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

17 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
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  6. Experimental Approaches to Visualize Effector Protein Translocation During Host-Pathogen Interactions.BioEssays : news and reviews in molecular, cellular and developmental biology · 2025
    Review
  7. Bacterial aggregation facilitates internalin-mediated invasion ofFrontiers in cellular and infection microbiology · 2024
    Article
  8. Article
  9. Article
  10. Autotrophic lactate production from HApplied microbiology and biotechnology · 2022
    Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. The T3SS ofMicroorganisms · 2020
    Review
  16. Article
  17. 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

7 authors at 1 institution in 1 country.

Caroline Peron-CaneLaboratoire de Physique de l'École normale supérieure, ENS, Université PSL, CNRS, Sorbonne Université, Université de Paris, Paris, France.ORCID 0000-0001-5185-117X
José-Carlos FernandezInstitut de biologie de l'ENS (IBENS), École normale supérieure, CNRS, INSERM, Université PSL, Paris, France.ORCID 0000-0003-2410-6179
Julien LeblancInstitut de biologie de l'ENS (IBENS), École normale supérieure, CNRS, INSERM, Université PSL, Paris, France.
Laure WingertsmannInstitut de biologie de l'ENS (IBENS), École normale supérieure, CNRS, INSERM, Université PSL, Paris, France.
Arnaud GautierSorbonne Université, École normale supérieure, Université PSL, CNRS, Laboratoire des Biomolécules, LBM, Paris, France.ORCID 0000-0003-1017-9879
Nicolas DespratLaboratoire de Physique de l'École normale supérieure, ENS, Université PSL, CNRS, Sorbonne Université, Université de Paris, Paris, France.ORCID 0000-0002-5016-9360
Alice LebretonInstitut de biologie de l'ENS (IBENS), École normale supérieure, CNRS, INSERM, Université PSL, Paris, France.ORCID 0000-0002-6643-902X
Centre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Real-time imaging of bacterial virulence factor dynamics is hampered by the limited number of fluorescent tools suitable for tagging secreted effectors. Here, we demonstrated that the fluorogenic reporter FAST could be used to tag secreted proteins, and we implemented it to monitor infection dynamics in epithelial cells exposed to the human pathogen Listeria monocytogenes (Lm). By tracking individual FAST-labelled vacuoles after Lm internalisation into cells, we unveiled the heterogeneity of residence time inside entry vacuoles. Although half of the bacterial population escaped within 13 minutes after entry, 12% of bacteria remained entrapped over an hour inside long term vacuoles, and sometimes much longer, regardless of the secretion of the pore-forming toxin listeriolysin O (LLO). We imaged LLO-FAST in these long-term vacuoles, and showed that LLO enabled Lm to proliferate inside these compartments, reminiscent of what had been previously observed for Spacious Listeria-containing phagosomes (SLAPs). Unexpectedly, inside epithelial SLAP-like vacuoles (eSLAPs), Lm proliferated as fast as in the host cytosol. eSLAPs thus constitute an alternative replication niche in epithelial cells that might promote the colonization of host tissues.

Indexed as

Bacterial ProteinsBacterial ToxinsCaco-2 CellsCell LineCell ProliferationCytosolEpithelial CellsFluorescent DyesHeat-Shock ProteinsHemolysin ProteinsHumansListeria monocytogenesListeriosisMacrophagesPhagosomesVacuolesBacterial ProteinsBacterial ToxinsFluorescent DyesHeat-Shock ProteinsHemolysin ProteinshlyA protein, Listeria monocytogenesVirulence Factors

Identifiers

PMID33045003
PMCPMC7580998
OpenAlexW3091886704

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.