Evidence map›Paper›PMID 25887115›Full record

ArticleBMC genomics2015

Comprehensive molecular, genomic and phenotypic analysis of a major clone of Enterococcus faecalis MLST ST40.

Melanie Zischka, Carsten T Künne, Jochen Blom, Dominique Wobser, Türkân Sakιnç, Kerstin Schmidt-Hohagen, P Wojtek Dabrowski, Andreas Nitsche, Johannes Hübner, Torsten Hain and 22 more

Abstract read
In one paragraph

Article in BMC genomics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
–field-weighted citation impact
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

23 citing papers in PubMed.

  1. Article
  2. Hidden diversity inMicrobiology spectrum · 2025
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  3. Insights into ecology, pathogenesis, and biofilm formation ofMicrobiology and molecular biology reviews : MMBR · 2025
    Review
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  5. CRISPR-Cas systems in enterococci.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2024
    Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. A Genomic Snapshot of Antibiotic-ResistantGlobal health, epidemiology and genomics · 2023
    Article
  11. Review
  12. Review
  13. Article
  14. Molecular Characterization ofFrontiers in microbiology · 2021
    Article
  15. Prevalence of an Intestinal ST40International journal of molecular sciences · 2020
    Article
  16. Comparative genomics of globalMicrobial genomics · 2020
    Article
  17. Genomic analysis of multidrug-resistant clinicalAntimicrobial resistance and infection control · 2019
    Article
  18. Article
  19. Article
  20. A genomic view of food-related and probiotic Enterococcus strains.DNA research : an international journal for rapid publication of reports on genes and genomes · 2017
    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

32 authors.

Melanie ZischkaDivision of Nosocomial Pathogens and Antibiotic Resistances, Department of Infectious Diseases, Robert Koch Institute, Wernigerode Branch, Burgstr. 37, D-38855, Wernigerode, Germany. melanie.zischka@googlemail.com.
Carsten T KünneFunctional Genomics of Bacterial Pathogens, Institute for Medical Microbiology, Justus Liebig University Giessen and German Center for Infection Research (DZIF), Partner site Giessen-Marburg-Langen, Campus Giessen, Giessen, Germany. Carsten.Kuenne@mikrobio.med.uni-giessen.de.
Jochen BlomCenter for Biotechnology (CeBiTec)/University of Bielefeld, Bielefeld, Germany. jochen.blom@computational.bio.uni-giessen.de.
Dominique WobserDivision of Infectious Diseases, Department of Medicine, University Hospital Freiburg, Freiburg, Germany. dominique.wobser@googlemail.com.
Türkân SakιnçDivision of Infectious Diseases, Department of Medicine, University Hospital Freiburg, Freiburg, Germany. tuersak@googlemail.com.
Kerstin Schmidt-HohagenInstitute for Biochemistry, Biotechnology and Bioinformatics, Technische Universität Braunschweig, Braunschweig, Germany. k.schmidt-hohagen@tu-braunschweig.de.
P Wojtek DabrowskiRobert Koch Institute, ZBS 1 Highly Pathogenic Viruses, Centre for Biological Threats and Special Pathogens, Berlin, Germany. dabrowskiw@rki.de.
Andreas NitscheRobert Koch Institute, ZBS 1 Highly Pathogenic Viruses, Centre for Biological Threats and Special Pathogens, Berlin, Germany. nitschea@rki.de.
Johannes HübnerDivision of Infectious Diseases, Department of Medicine, University Hospital Freiburg, Freiburg, Germany. johueb@gmail.com.
Torsten HainFunctional Genomics of Bacterial Pathogens, Institute for Medical Microbiology, Justus Liebig University Giessen and German Center for Infection Research (DZIF), Partner site Giessen-Marburg-Langen, Campus Giessen, Giessen, Germany. torsten.hain@mikrobio.med.uni-giessen.de.
Trinad ChakrabortyFunctional Genomics of Bacterial Pathogens, Institute for Medical Microbiology, Justus Liebig University Giessen and German Center for Infection Research (DZIF), Partner site Giessen-Marburg-Langen, Campus Giessen, Giessen, Germany. Trinad.Chakraborty@mikrobio.med.uni-giessen.de.
Burkhard LinkeCenter for Biotechnology (CeBiTec)/University of Bielefeld, Bielefeld, Germany. burkhard.linke@computational.bio.uni-giessen.de.
Alexander GoesmannCenter for Biotechnology (CeBiTec)/University of Bielefeld, Bielefeld, Germany. Alexander.Goesmann@computational.bio.uni-giessen.de.
Sonja VogetGoettingen Genomics Laboratory, Georg August University, Goettingen, Germany. svoget@uni-goettingen.de.
Rolf DanielGoettingen Genomics Laboratory, Georg August University, Goettingen, Germany. rdaniel@gwdg.de.
Dietmar SchomburgInstitute for Biochemistry, Biotechnology and Bioinformatics, Technische Universität Braunschweig, Braunschweig, Germany. d.schomburg@tu-bs.de.
Rüdiger HauckDepartment of Veterinary Medicine, Institute for Poultry Diseases, Free University Berlin, Berlin, Germany. ruediger.hauck@bvl.bund.de.
Hafez M HafezDepartment of Veterinary Medicine, Institute for Poultry Diseases, Free University Berlin, Berlin, Germany. Hafez.Mohamed@fu-berlin.de.
Petra TielenInstitute for Microbiology, Technische Universität Braunschweig, Braunschweig, Germany. petra.tielen@googlemail.com.
Dieter JahnInstitute for Microbiology, Technische Universität Braunschweig, Braunschweig, Germany. d.jahn@tu-bs.de.
Margrete SolheimLaboratory of Microbial Gene Technology and Food Microbiology, The Norwegian University of Life Sciences, Ås, Norway. margrete.solheim@umb.no.
Ewa SadowyNational Medicines Institute, Warsaw, Poland. ewasadowy@cls.edu.pl.
Jesper LarsenStatens Serum Institute, Copenhagen, Denmark. JRL@ssi.dk.
Lars B JensenDivision of Microbiology, National Food Institute, Danish Technical University, Copenhagen, Denmark. LJE@food.dtu.dk.
Patricia Ruiz-GarbajosaDepartment of Microbiology, Hospital Ramon y Cajal, Madrid, Spain. patruizg@gmail.com.
Dianelys Quiñones PérezInstituto de Medicina Tropical Pedro Kourí, Servicio de Bacteriología-Micología, La Habana, Cuba. Dia@ipk.sld.cu.
Theresa MikalsenDepartment of Medical Biology, Faculty of Health Sciences, Research Group for Host Microbe Interactions, University of Tromsø, Tromsø, Norway. theresa.mikalsen@uit.no.
Jennifer BenderDivision of Nosocomial Pathogens and Antibiotic Resistances, Department of Infectious Diseases, Robert Koch Institute, Wernigerode Branch, Burgstr. 37, D-38855, Wernigerode, Germany. benderj@rki.de.
Matthias SteglichDivision of Nosocomial Pathogens and Antibiotic Resistances, Department of Infectious Diseases, Robert Koch Institute, Wernigerode Branch, Burgstr. 37, D-38855, Wernigerode, Germany. steglichm@rki.de.
Ulrich NübelDivision of Nosocomial Pathogens and Antibiotic Resistances, Department of Infectious Diseases, Robert Koch Institute, Wernigerode Branch, Burgstr. 37, D-38855, Wernigerode, Germany. uln14@dsmz.de.
Wolfgang WitteDivision of Nosocomial Pathogens and Antibiotic Resistances, Department of Infectious Diseases, Robert Koch Institute, Wernigerode Branch, Burgstr. 37, D-38855, Wernigerode, Germany. wittew@rki.de.
Guido WernerDivision of Nosocomial Pathogens and Antibiotic Resistances, Department of Infectious Diseases, Robert Koch Institute, Wernigerode Branch, Burgstr. 37, D-38855, Wernigerode, Germany. wernerg@rki.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEnterococcus faecalis is a multifaceted microorganism known to act as a beneficial intestinal commensal bacterium. It is also a dreaded nosocomial pathogen causing life-threatening infections in hospitalised patients. Isolates of a distinct MLST type ST40 represent the most frequent strain type of this species, distributed worldwide and originating from various sources (animal, human, environmental) and different conditions (colonisation/infection). Since enterococci are known to be highly recombinogenic we determined to analyse the microevolution and niche adaptation of this highly distributed clonal type.

resultsWe compared a set of 42 ST40 isolates by assessing key molecular determinants, performing whole genome sequencing (WGS) and a number of phenotypic assays including resistance profiling, formation of biofilm and utilisation of carbon sources. We generated the first circular closed reference genome of an E. faecalis isolate D32 of animal origin and compared it with the genomes of other reference strains. D32 was used as a template for detailed WGS comparisons of high-quality draft genomes of 14 ST40 isolates. Genomic and phylogenetic analyses suggest a high level of similarity regarding the core genome, also demonstrated by similar carbon utilisation patterns. Distribution of known and putative virulence-associated genes did not differentiate between ST40 strains from a commensal and clinical background or an animal or human source. Further analyses of mobile genetic elements (MGE) revealed genomic diversity owed to: (1) a modularly structured pathogenicity island; (2) a site-specifically integrated and previously unknown genomic island of 138 kb in two strains putatively involved in exopolysaccharide synthesis; and (3) isolate-specific plasmid and phage patterns. Moreover, we used different cell-biological and animal experiments to compare the isolate D32 with a closely related ST40 endocarditis isolate whose draft genome sequence was also generated. D32 generally showed a greater capacity of adherence to human cell lines and an increased pathogenic potential in various animal models in combination with an even faster growth in vivo (not in vitro).

conclusionMolecular, genomic and phenotypic analysis of representative isolates of a major clone of E. faecalis MLST ST40 revealed new insights into the microbiology of a commensal bacterium which can turn into a conditional pathogen.

Indexed as

Genome, BacterialAnimalsBacteremiaBacterial AdhesionBiofilmsCaco-2 CellsCarbonCRISPR-Cas SystemsEnterococcus faecalisFemaleGenomicsGram-Positive Bacterial InfectionsHumansInterspersed Repetitive SequencesLepidopteraMice, Inbred BALB CCarbon

Identifiers

PMID25887115
PMCPMC4374294

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Registered trials

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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.