Evidence map›Paper›PMID 27275944›Full record

ArticlePloS one2016

Phenol-Soluble Modulins Contribute to Early Sepsis Dissemination Not Late Local USA300-Osteomyelitis Severity in Rabbits.

Benjamin Davido, Azzam Saleh-Mghir, Frédéric Laurent, Claire Danel, Florence Couzon, Laure Gatin, François Vandenesch, Jean-Philippe Rasigade, Anne-Claude Crémieux

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.4field-weighted citation impact, top 33% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Osteomyelitis.Nature reviews. Disease primers · 2026
    Review
  2. Review
  3. The endothelium at the interface between tissues andClinical microbiology reviews · 2025
    Review
  4. Article
  5. Genotypic and Phenotypic Characterization of SomeInfection and drug resistance · 2023
    Article
  6. Article
  7. Review
  8. Toxins · 2021
    Review
  9. Article
  10. Article
  11. Article
  12. The Process of Osteoblastic Infection byInternational journal of medical sciences · 2020
    Review
  13. Understanding the Virulence ofFrontiers in cellular and infection microbiology · 2018
    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 5 institutions in 1 country.

Benjamin DavidoDépartement de Médecine Aigüe Spécialisée, Hôpital Universitaire Raymond-Poincaré, Assistance Publique-Hôpitaux de Paris, Garches, and EA 3647, Faculté de Médecine Paris-Île-de-France Ouest, Université Versailles-Saint-Quentin, Versailles, France.
Azzam Saleh-MghirDépartement de Médecine Aigüe Spécialisée, Hôpital Universitaire Raymond-Poincaré, Assistance Publique-Hôpitaux de Paris, Garches, and EA 3647, Faculté de Médecine Paris-Île-de-France Ouest, Université Versailles-Saint-Quentin, Versailles, France.
Frédéric LaurentCIRI, International Center for Infectiology Research, Inserm U1111-CNRS UMR5308, ENS Lyon-Université Lyon 1, Hospices Civils de Lyon, Lyon, France.
Claire DanelDépartement de Pathologie, UFR de Médecine Paris 7, site Bichat, Paris, France.
Florence CouzonCIRI, International Center for Infectiology Research, Inserm U1111-CNRS UMR5308, ENS Lyon-Université Lyon 1, Hospices Civils de Lyon, Lyon, France.
Laure GatinDépartement de Médecine Aigüe Spécialisée, Hôpital Universitaire Raymond-Poincaré, Assistance Publique-Hôpitaux de Paris, Garches, and EA 3647, Faculté de Médecine Paris-Île-de-France Ouest, Université Versailles-Saint-Quentin, Versailles, France.
François VandeneschCIRI, International Center for Infectiology Research, Inserm U1111-CNRS UMR5308, ENS Lyon-Université Lyon 1, Hospices Civils de Lyon, Lyon, France.
Jean-Philippe RasigadeCIRI, International Center for Infectiology Research, Inserm U1111-CNRS UMR5308, ENS Lyon-Université Lyon 1, Hospices Civils de Lyon, Lyon, France.
Anne-Claude CrémieuxDépartement de Médecine Aigüe Spécialisée, Hôpital Universitaire Raymond-Poincaré, Assistance Publique-Hôpitaux de Paris, Garches, and EA 3647, Faculté de Médecine Paris-Île-de-France Ouest, Université Versailles-Saint-Quentin, Versailles, France.
Centre International de Recherche en Infectiologie · FRHôpital Raymond-Poincaré · FRInfection et inflammation · FRUniversité Claude Bernard Lyon 1 · FRHôpital Bichat-Claude-Bernard · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionIn bone and joint infections (BJIs), bacterial toxins are major virulence factors: Panton-Valentine leukocidin (PVL) expression leads to severe local damage, including bone distortion and abscesses, while α-hemolysin (Hla) production is associated with severe sepsis-related mortality. Recently, other toxins, namely phenol-soluble modulins (PSMs) expressed by community-associated methicillin-resistant Staphylococcus aureus (CA-MRSA) strain USA300 (LAC WT) were shown to have ex vivo intracellular cytotoxic activity after S. aureus invasion of osteoblasts, but their in vivo contribution in a relatively PVL-sensitive osteomyelitis model remains poorly elucidated. MATERIALS AND

methodsWe compared the outcomes of experimental rabbit osteomyelitises induced with pvl+hla+psms+ LAC WT and its isogenic Δpsm derivatives (LAC Δpsmα and LAC Δpsmαβhld) using an inoculum of 3 × 108 CFUs. Mortality, hematogenous spread (blood culture, spleen and kidney), lung and bone involvements were assessed in two groups (non-survivors of severe sepsis and survivors sacrificed on day (D) 14).

resultsSevere sepsis-related mortality tended to be lower for Δpsm derivatives (Kaplan-Meier curves, P = .06). Non-survivors' bone LAC-Δpsmα (6.9 log10 CFUs/g of bone, P = .04) or -Δpsmαβhld (6.86 log10 CFUs/g of bone, P = .014) densities were significantly higher than LAC WT (6.43 log10 CFUs/g of bone). Conversely, lung Δpsmαβhld CFUs were significantly lower than LAC WT (P = .04). LAC Δpsmα, Δpsmαβhld and WT induced similar bone damage in D14 survivors, with comparable bacterial densities (respectively: 5.89, 5.91, and 6.15 log10 CFUs/g of bone). Meanwhile, pulmonary histological scores of inflammation were significantly higher for LAC Δpsmα- and Δpsmαβhld-infected rabbits compared to LAC WT (P = .04 and .01, respectively) but with comparable lung bacterial densities.

conclusionOur experimental results showed that deactivating PSM peptides significantly limited bacterial dissemination from bone during the early phase of infection, but did not affect local severity of USA300 rabbit osteomyelitis.

Indexed as

Bacterial ToxinsMethicillin-Resistant Staphylococcus aureusOsteomyelitisSepsisStaphylococcal InfectionsAnimalsDisease Models, AnimalRabbitsBacterial Toxins

Identifiers

PMID27275944
PMCPMC4898696
OpenAlexW2415312662

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.