Evidence map›Paper›PMID 30487573›Full record

ArticleNature communications2018

Disease-associated genotypes of the commensal skin bacterium Staphylococcus epidermidis.

Guillaume Méric, Leonardos Mageiros, Johan Pensar, Maisem Laabei, Koji Yahara, Ben Pascoe, Nattinee Kittiwan, Phacharaporn Tadee, Virginia Post, Sarah Lamble and 15 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 105 papers.

0numbers the graph read from it
0cells of the map it votes in
105citing papers in PubMed
11.4field-weighted citation impact, top 1% 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

105 citing papers in PubMed, 185 citations in OpenAlex.

  1. Strain-level genomic analysis ofMicrobiology spectrum · 2026
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  9. Pharmaceutics · 2026
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  20. Methicillin-sensitiveMicrobial genomics · 2025
    Article

45 more citing papers are in PubMed but not listed here.

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

25 authors at 16 institutions in 10 countries.

Guillaume MéricThe Milner Centre for Evolution, University of Bath, Claverton Down, Bath, BA2 7AY, UK.
Leonardos MageirosThe Milner Centre for Evolution, University of Bath, Claverton Down, Bath, BA2 7AY, UK.
Johan PensarDepartment of Mathematics and Statistics, University of Helsinki, Helsinki, 00100, Finland.
Maisem LaabeiThe Milner Centre for Evolution, University of Bath, Claverton Down, Bath, BA2 7AY, UK.
Koji YaharaAntimicrobial Resistance Research Center, National Institute of Infectious Diseases, Tokyo, 162-8640, Japan.
Ben PascoeThe Milner Centre for Evolution, University of Bath, Claverton Down, Bath, BA2 7AY, UK.ORCID http://orcid.org/0000-0001-6376-5121
Nattinee KittiwanIntegrative Research Centre for Veterinary Preventive Medicine, Faculty of Veterinary Medicine, Chiang Mai University, Chiang Mai, 50200, Thailand.
Phacharaporn TadeeGraduate School, Maejo University, Chiang Mai, 50290, Thailand.
Virginia PostAO Research Institute Davos, Davos, 7270, Switzerland.
Sarah LambleWellcome Centre for Human Genetics, University of Oxford, Oxford, OX3 7BN, UK.
Rory BowdenWellcome Centre for Human Genetics, University of Oxford, Oxford, OX3 7BN, UK.ORCID http://orcid.org/0000-0001-8596-0366
James E BrayDepartment of Zoology, University of Oxford, Oxford, OX1 3SZ, UK.ORCID http://orcid.org/0000-0003-3554-4254
Mario MorgensternDepartment of Orthopaedic Surgery and Traumatology, University Hospital Basel, Basel, 4031, Switzerland.
Keith A JolleyDepartment of Zoology, University of Oxford, Oxford, OX1 3SZ, UK.ORCID http://orcid.org/0000-0002-0751-0287
Martin C J MaidenDepartment of Zoology, University of Oxford, Oxford, OX1 3SZ, UK.ORCID http://orcid.org/0000-0001-6321-5138
Edward J FeilThe Milner Centre for Evolution, University of Bath, Claverton Down, Bath, BA2 7AY, UK.ORCID http://orcid.org/0000-0003-1446-6744
Xavier DidelotDepartment of Infectious Disease Epidemiology, Imperial College, London, SW7 2AZ, UK.
Maria MiragaiaLaboratory of Molecular Genetics, Instituto de Tecnologia Química e Biológica, Universidade Nova de Lisboa, Oeiras, 2775-412, Portugal.
Herminia de LencastreLaboratory of Molecular Genetics, Instituto de Tecnologia Química e Biológica, Universidade Nova de Lisboa, Oeiras, 2775-412, Portugal.
T Fintan MoriartyAO Research Institute Davos, Davos, 7270, Switzerland.ORCID http://orcid.org/0000-0003-2307-0397
Holger RohdeInstitut für Medizinische Mikrobiologie, Virologie & Hygiene, Universität Hamburg, Hamburg, 20246, Germany.
Ruth MasseyThe Milner Centre for Evolution, University of Bath, Claverton Down, Bath, BA2 7AY, UK.
Dietrich MackBioscientia Labor Ingelheim, Institut für Medizinische Diagnostik GmbH, Ingelheim, 55218, Germany.
Jukka CoranderDepartment of Mathematics and Statistics, University of Helsinki, Helsinki, 00100, Finland.ORCID http://orcid.org/0000-0002-7752-1942
Samuel K SheppardThe Milner Centre for Evolution, University of Bath, Claverton Down, Bath, BA2 7AY, UK. s.k.sheppard@bath.ac.uk.
University of Oxford · GBUniversity of Bath · GBAO Foundation · CHCentre for Human Genetics · GBStatistics Finland · FIChiang Mai University · THImperial College London · GBMaejo University · THMalmö University · SENational Institute of Infectious Diseases · JPRockefeller University · USSwansea University · GBUniversidade Nova de Lisboa · PTUniversität Hamburg · DEUniversity Hospital of Basel · CHUniversity of Bristol · GB

Funding

Medical Research Council G0801929Medical Research Council MR/L015080/1Medical Research Council MR/M501608/1Medical Research Council MR/R015600/1Wellcome Trust
6 · The paper itself

Abstract

Some of the most common infectious diseases are caused by bacteria that naturally colonise humans asymptomatically. Combating these opportunistic pathogens requires an understanding of the traits that differentiate infecting strains from harmless relatives. Staphylococcus epidermidis is carried asymptomatically on the skin and mucous membranes of virtually all humans but is a major cause of nosocomial infection associated with invasive procedures. Here we address the underlying evolutionary mechanisms of opportunistic pathogenicity by combining pangenome-wide association studies and laboratory microbiology to compare S. epidermidis from bloodstream and wound infections and asymptomatic carriage. We identify 61 genes containing infection-associated genetic elements (k-mers) that correlate with in vitro variation in known pathogenicity traits (biofilm formation, cell toxicity, interleukin-8 production, methicillin resistance). Horizontal gene transfer spreads these elements, allowing divergent clones to cause infection. Finally, Random Forest model prediction of disease status (carriage vs. infection) identifies pathogenicity elements in 415 S. epidermidis isolates with 80% accuracy, demonstrating the potential for identifying risk genotypes pre-operatively.

Indexed as

Genome, BacterialGenome-Wide Association StudyGenotypeHumansInterleukin-8Skin DiseasesStaphylococcal InfectionsStaphylococcus epidermidisInterleukin-8

Identifiers

PMID30487573
PMCPMC6261936
OpenAlexW2900896766

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.