Evidence map›Paper›PMID 26322633›Full record

ArticlePloS one2015

Characterization of Two Metal Binding Lipoproteins as Vaccine Candidates for Enterococcal Infections.

Felipe Romero-Saavedra, Diana Laverde, Aurélie Budin-Verneuil, Cécile Muller, Benoit Bernay, Abdellah Benachour, Axel Hartke, Johannes Huebner

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. 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
1.4field-weighted citation impact, top 20% 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, 38 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Enterococcal Membrane Vesicles as Vaccine Candidates.International journal of molecular sciences · 2023
    Article
  8. Article
  9. Article
  10. Review
  11. Mucosal Vaccination withVaccines · 2020
    Article
  12. Review
  13. Article
  14. Article
  15. Article
  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

8 authors at 3 institutions in 2 countries.

Felipe Romero-SaavedraDivision of Infectious Diseases, Department of Medicine, University Medical Center Freiburg, Freiburg, Germany; EA4655 U2RM Stress/Virulence, University of Caen Lower-Normandy, Caen, France.
Diana LaverdeDivision of Infectious Diseases, Department of Medicine, University Medical Center Freiburg, Freiburg, Germany; EA4655 U2RM Stress/Virulence, University of Caen Lower-Normandy, Caen, France.
Aurélie Budin-VerneuilEA4655 U2RM Stress/Virulence, University of Caen Lower-Normandy, Caen, France.
Cécile MullerEA4655 U2RM Stress/Virulence, University of Caen Lower-Normandy, Caen, France.
Benoit BernayProteogen platform SFR ICORE 4206, University of Caen Lower-Normandy, Caen, France.
Abdellah BenachourEA4655 U2RM Stress/Virulence, University of Caen Lower-Normandy, Caen, France.
Axel HartkeEA4655 U2RM Stress/Virulence, University of Caen Lower-Normandy, Caen, France.
Johannes HuebnerDivision of Infectious Diseases, Department of Medicine, University Medical Center Freiburg, Freiburg, Germany; Division of Pediatric Infectious Diseases, Dr. von Hauner Children's Hospital, Ludwig-Maximilians-University, Munich, Germany.
Université de Caen Normandie · FRLudwig-Maximilians-Universität München · DEUniversity Medical Center Freiburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEnterococcus faecium and faecalis are Gram-positive opportunistic pathogens that have become leading causes of nosocomial infections over the last decades. Especially multidrug resistant enterococci have become a challenging clinical problem worldwide. Therefore, new treatment options are needed and the identification of alternative targets for vaccine development has emerged as a feasible alternative to fight the infections caused by these pathogens.

resultsWe extrapolate the transcriptomic data from a mice peritonitis infection model in E. faecalis to identify putative up-regulated surface proteins under infection conditions in E. faecium. After the bionformatic analyses two metal binding lipoproteins were identified to have a high homology (>72%) between the two species, the manganese ABC transporter substrate-binding lipoprotein (PsaAfm,) and the zinc ABC transporter substrate-binding lipoprotein (AdcAfm). These candidate lipoproteins were overexpressed in Escherichia coli and purified. The recombinant proteins were used to produce rabbit polyclonal antibodies that were able to induce specific opsonic antibodies that mediated killing of the homologous strain E. faecium E155 as well as clinical strains E. faecium E1162, Enterococcus faecalis 12030, type 2 and type 5. Mice were passively immunized with the antibodies raised against recombinant lipoproteins, showing significant reduction of colony counts in mice livers after the bacterial challenge and demonstrating the efficacy of these metal binding lipoproteins as promising vaccine candidates to treat infections caused by these enterococcal pathogens.

conclusionOverall, our results demonstrate that these two metal binding lipoproteins elicited specific, opsonic and protective antibodies, with an extensive cross-reactivity and serotype-independent coverage among these two important nocosomial pathogens. Pointing these two protein antigens as promising immunogens, that can be used as single components or as carrier proteins together with polysaccharide antigens in vaccine development against enterococcal infections.

Indexed as

AnimalsAntibodies, BacterialAntigens, BacterialATP-Binding Cassette TransportersBacterial VaccinesCation Transport ProteinsEnterococcus faecalisEnterococcus faeciumFemaleGram-Positive Bacterial InfectionsImmunoglobulin GLipoproteinsManganeseMiceMice, Inbred BALB COpsonin ProteinsAntibodies, BacterialAntigens, BacterialATP-Binding Cassette TransportersBacterial VaccinesCation Transport ProteinsImmunoglobulin GLipoproteinsManganeseOpsonin ProteinsZinc

Identifiers

PMID26322633
PMCPMC4556446
OpenAlexW2170910952

What OpenQuestion holds

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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.