Evidence map›Paper›PMID 28456423›Full record

ArticleEBioMedicine2017

Staphylococcus aureus Promotes Smed-PGRP-2/Smed-setd8-1 Methyltransferase Signalling in Planarian Neoblasts to Sensitize Anti-bacterial Gene Responses During Re-infection.

Cedric Torre, Prasad Abnave, Landry Laure Tsoumtsa, Giovanna Mottola, Catherine Lepolard, Virginie Trouplin, Gregory Gimenez, Julie Desrousseaux, Stephanie Gempp, Anthony Levasseur and 3 more

Open access · goldAbstract read
In one paragraph

Article in EBioMedicine, 2017. 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
1.8field-weighted citation impact, top 15% 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, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Chromatin-derived histone proteins fromFrontiers in cellular and infection microbiology · 2026
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  8. Article
  9. A pan-metazoan concept for adult stem cells: the wobbling Penrose landscape.Biological reviews of the Cambridge Philosophical Society · 2022
    Article
  10. Article
  11. The Role of PPAR Alpha in the Modulation of Innate Immunity.International journal of molecular sciences · 2021
    Review
  12. Review
  13. Review
  14. Article
  15. PeerJ · 2020
    Article
  16. Article
  17. Epigenetics and Trained Immunity.Antioxidants & redox signaling · 2018
    Review
  18. Article
  19. Article
  20. Trained Immunity Carried by Non-immune Cells.Frontiers in microbiology · 2018
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 7 institutions in 2 countries.

Cedric TorreCNRS UMR 7278, IRD198, INSERM U1095, APHM, Institut Hospitalier Universitaire Méditerranée-Infection, Aix-Marseille Université, 19-21 Bd Jean Moulin 13385, Marseille, Cedex 05, France.
Prasad AbnaveCNRS UMR 7278, IRD198, INSERM U1095, APHM, Institut Hospitalier Universitaire Méditerranée-Infection, Aix-Marseille Université, 19-21 Bd Jean Moulin 13385, Marseille, Cedex 05, France.
Landry Laure TsoumtsaCNRS UMR 7278, IRD198, INSERM U1095, APHM, Institut Hospitalier Universitaire Méditerranée-Infection, Aix-Marseille Université, 19-21 Bd Jean Moulin 13385, Marseille, Cedex 05, France.
Giovanna MottolaUMR MD2, Faculté de Médecine Nord, Aix Marseille University and Institute of Research in Biology of the French Army Marseille, France; Laboratory of Biochemistry, La Timone University Hospital, Assistance Publique Hôpitaux de Marseille, Marseille, France.
Catherine LepolardCNRS UMR 7278, IRD198, INSERM U1095, APHM, Institut Hospitalier Universitaire Méditerranée-Infection, Aix-Marseille Université, 19-21 Bd Jean Moulin 13385, Marseille, Cedex 05, France.
Virginie TrouplinCNRS UMR 7278, IRD198, INSERM U1095, APHM, Institut Hospitalier Universitaire Méditerranée-Infection, Aix-Marseille Université, 19-21 Bd Jean Moulin 13385, Marseille, Cedex 05, France.
Gregory GimenezOtago Genomics & Bioinformatics Facility, Department of Biochemistry, University of Otago, PO Box 56, 710 Cumberland Street, Dunedin 9054, New Zealand.
Julie DesrousseauxAPHM, Timone Hospital, Department of Radiotherapy, Marseille 13005, France.
Stephanie GemppAPHM, Timone Hospital, Department of Radiotherapy, Marseille 13005, France.
Anthony LevasseurCNRS UMR 7278, IRD198, INSERM U1095, APHM, Institut Hospitalier Universitaire Méditerranée-Infection, Aix-Marseille Université, 19-21 Bd Jean Moulin 13385, Marseille, Cedex 05, France.
Laetitia PadovaniAPHM, Timone Hospital, Department of Radiotherapy, Marseille 13005, France.
Emmanuel LemichezUCA, Inserm, U1065, C3M, Université de Nice Sophia-Antipolis, Equipe labellisée Ligue Contre le Cancer, 06204 Nice Cedex 3, France.
Eric GhigoCNRS UMR 7278, IRD198, INSERM U1095, APHM, Institut Hospitalier Universitaire Méditerranée-Infection, Aix-Marseille Université, 19-21 Bd Jean Moulin 13385, Marseille, Cedex 05, France. Electronic address: eric.ghigo@univ-amu.fr.
Aix-Marseille Université · FRHôpital de la Timone · FRInserm · FRUnité de Recherche sur les Maladies Infectieuses et Tropicales Emergentes · FRCentre d’Immunologie de Marseille-Luminy · FRCentre National de la Recherche Scientifique · FRMéditerranée Infection Foundation · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Little is known about how organisms exposed to recurrent infections adapt their innate immune responses. Here, we report that planarians display a form of instructed immunity to primo-infection by Staphylococcus aureus that consists of a transient state of heightened resistance to re-infection that persists for approximately 30days after primo-infection. We established the involvement of stem cell-like neoblasts in this instructed immunity using the complementary approaches of RNA-interference-mediated cell depletion and tissue grafting-mediated gain of function. Mechanistically, primo-infection leads to expression of the peptidoglycan receptor Smed-PGRP-2, which in turn promotes Smed-setd8-1 histone methyltransferase expression and increases levels of lysine methylation in neoblasts. Depletion of neoblasts did not affect S. aureus clearance in primo-infection but, in re-infection, abrogated the heightened elimination of bacteria and reduced Smed-PGRP-2 and Smed-setd8-1 expression. Smed-PGRP-2 and Smed-setd8-1 sensitize animals to heightened expression of Smed-p38 MAPK and Smed-morn2, which are downstream components of anti-bacterial responses. Our study reveals a central role of neoblasts in innate immunity against S. aureus to establish a resistance state facilitating Smed-sted8-1-dependent expression of anti-bacterial genes during re-infection.

Indexed as

Signal TransductionAnimalsCarrier ProteinsDisease ResistanceGene ExpressionGene Expression RegulationHost-Pathogen InteractionsPlanariansProtein MethyltransferasesStaphylococcus aureusStem CellsCarrier Proteinspeptidoglycan recognition proteinProtein MethyltransferasesInstructed immunityNeoblastsPGRP-2PlanariansS. aureussted8-1Stem cells

Identifiers

PMID28456423
PMCPMC5478204
OpenAlexW2609000266

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.