Evidence map›Paper›PMID 28444231›Full record

ArticleGenome biology and evolution2017

Whole-Genome Sequencing of Seven Strains of Staphylococcus lugdunensis Allows Identification of Mobile Genetic Elements.

Xavier Argemi, Véronique Martin, Valentin Loux, Sandrine Dahyot, Jérémie Lebeurre, Aurélien Guffroy, Mickael Martin, Aurélie Velay, Daniel Keller, Philippe Riegel and 3 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Genome biology and evolution, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02026895 (Virulence of Staphylococcus Lugdunensis in Severe Infections), which is not on this map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.6field-weighted citation impact, top 18% 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.

NCT02026895 nacompletednot on this map

Virulence of Staphylococcus Lugdunensis in Severe Infections

TypeinterventionalSponsorUniversity Hospital, Strasbourg, FranceRan2013 to 2016Enrolled82ConditionsStaphylococcus Lugdunensis, Bacteremia, Endocarditis, Virulence FactorsArmsGenetic blood sample
3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Global genomic landscape ofApplied and environmental microbiology · 2026
    Article
  2. Article
  3. Searching for Virulence Factors amongInternational journal of molecular sciences · 2023
    Article
  4. Article
  5. Identification of New Drug Target inBioengineering (Basel, Switzerland) · 2022
    Article
  6. Article
  7. Article
  8. Coagulase-Negative Staphylococci Pathogenomics.International journal of molecular sciences · 2019
    Review
  9. Comparative Genome Analysis ofFrontiers in microbiology · 2019
    Article
  10. Article
  11. Article
  12. Article
  13. Review
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

13 authors at 6 institutions in 1 country.

Xavier ArgemiHôpitaux Universitaires, Maladies Infectieuses et Tropicales, Strasbourg, France.
Véronique MartinINRA - Unité Mathématiques et Informatique Appliquées, du Genome à l'Environnement (MaIAGE), Jouy-en Josas, France.
Valentin LouxINRA - Unité Mathématiques et Informatique Appliquées, du Genome à l'Environnement (MaIAGE), Jouy-en Josas, France.
Sandrine DahyotLaboratoire GRAM EA2656, Université de Rouen - IRIB UFR Médecine-Pharmacie Batiment Recherche, Rouen, France.
Jérémie LebeurreLaboratoire GRAM EA2656, Université de Rouen - IRIB UFR Médecine-Pharmacie Batiment Recherche, Rouen, France.
Aurélien GuffroyService d'Immunologie Clinique et de Médecine Interne, Centre National de Référence des Maladies Auto-immunes Rares, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
Mickael MartinService d'Immunologie Clinique et de Médecine Interne, Centre National de Référence des Maladies Auto-immunes Rares, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
Aurélie VelayVirology Laboratory, University Hospital of Strasbourg, Strasbourg, France.
Daniel KellerUniversité de Strasbourg, CHRU de Strasbourg, VBP EA7290, Fédération de Médecine Translationnelle de Strasbourg (FMTS), Institut de bactériologie, Hôpitaux Universitaires de Strasbourg, France.
Philippe RiegelUniversité de Strasbourg, CHRU de Strasbourg, VBP EA7290, Fédération de Médecine Translationnelle de Strasbourg (FMTS), Institut de bactériologie, Hôpitaux Universitaires de Strasbourg, France.
Yves HansmannHôpitaux Universitaires, Maladies Infectieuses et Tropicales, Strasbourg, France.
Nicodème PaulLaboratoire d'ImmunoRhumatologie Moléculaire, INSERM UMR_S 1109, Plateforme GENOMAX, Faculté de Médecine, Fédération Hospitalo-Universitaire OMICARE, Fédération de Médecine Translationnelle de Strasbourg (FMTS), Université de Strasbourg, Strasbourg, France.
Gilles PrévostUniversité de Strasbourg, CHRU de Strasbourg, VBP EA7290, Fédération de Médecine Translationnelle de Strasbourg (FMTS), Institut de bactériologie, Hôpitaux Universitaires de Strasbourg, France.
Hôpitaux Universitaires de Strasbourg · FRImmunologie, Immunopathologie et Chimie Thérapeutique · FRInstitut de Virologie · FRMathématiques et Informatique Appliquées du Génome à l'Environnement · FRUniversité de Strasbourg · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Coagulase negative staphylococci are normal inhabitant of the human skin flora that account for an increasing number of infections, particularly hospital-acquired infections. Staphylococcus lugdunensis has emerged as a most virulent species causing various infections with clinical characteristics close to what clinicians usually observe with Staphylococcus aureus and both bacteria share more than 70% of their genome. Virulence of S. aureus relies on a large repertoire of virulence factors, many of which are encoded on mobile genetic elements. S. lugdunensis also bears various putative virulence genes but only one complete genome with extensive analysis has been published with one prophage sequence (φSL2) and a unique plasmid was previously described. In this study, we performed de novo sequencing, whole genome assembly and annotation of seven strains of S. lugdunensis from VISLISI clinical trial. We searched for the presence of virulence genes and mobile genetics elements using bioinformatics tools. We identified four new prophages, named φSL2 to φSL4, belonging to the Siphoviridae class and five plasmids, named pVISLISI_1 to pVISLISI_5. Three plasmids are homologous to known plasmids that include, amongst others, one S. aureus plasmid. The two other plasmids were not described previously. This study provides a new context for the study of S. lugdunensis virulence suggesting the occurrence of several genetic recombination' with other staphylococci.

Indexed as

Genome, BacterialGenomic IslandsInterspersed Repetitive SequencesMolecular Sequence AnnotationProphagesRecombination, GeneticStaphylococcal InfectionsStaphylococcus lugdunensisVirulence FactorsVirulence Factorsnext generation sequencingplasmidsprophagesStaphylococcus lugdunensisvirulence

Identifiers

PMID28444231
PMCPMC5425232
OpenAlexW2607319220

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

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.