Evidence map›Paper›PMID 38890594›Full record

ArticleBMC microbiology2024

Completed genome and emergence scenario of the multidrug-resistant nosocomial pathogen Staphylococcus epidermidis ST215.

Therese Kellgren, Chinmay Dwibedi, Micael Widerström, David Sundell, Caroline Öhrman, Andreas Sjödin, Tor Monsen, Patrik Rydén, Anders Johansson

Abstract read
In one paragraph

Article in BMC microbiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Active components ofFrontiers in cellular and infection microbiology · 2026
    Article
  3. Dissemination ofFrontiers in microbiology · 2025
    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.

Therese Kellgren *Department of Mathematics and Mathematical Statistics, Umeå University, Umeå, SE, 90187, Sweden.ORCID http://orcid.org/0000-0002-4911-7037
Chinmay Dwibedi *Department of Clinical Microbiology and Molecular Infection Medicine Sweden (MIMS), Umeå University, 90185, Umeå, Sweden.ORCID http://orcid.org/0000-0001-6416-4440
Micael WiderströmDepartment of Clinical Microbiology, Umeå University, 90185, Umeå, Sweden. micael.widerstrom@umu.se.ORCID http://orcid.org/0000-0002-1483-4255
David SundellDivision of CBRN Defence and Security, Swedish Defense Research Agency, 90182, Umeå, SE, Sweden.ORCID http://orcid.org/0000-0002-6269-0217
Caroline ÖhrmanDivision of CBRN Defence and Security, Swedish Defense Research Agency, 90182, Umeå, SE, Sweden.ORCID http://orcid.org/0000-0003-0516-7523
Andreas SjödinDivision of CBRN Defence and Security, Swedish Defense Research Agency, 90182, Umeå, SE, Sweden.ORCID http://orcid.org/0000-0001-5350-4219
Tor MonsenDepartment of Clinical Microbiology, Umeå University, 90185, Umeå, Sweden.ORCID http://orcid.org/0000-0001-8489-757X
Patrik RydénDepartment of Mathematics and Mathematical Statistics, Umeå University, Umeå, SE, 90187, Sweden.ORCID http://orcid.org/0000-0002-0577-123X
Anders JohanssonDepartment of Clinical Microbiology and Molecular Infection Medicine Sweden (MIMS), Umeå University, 90185, Umeå, Sweden.ORCID http://orcid.org/0000-0003-0548-5943

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA multidrug-resistant lineage of Staphylococcus epidermidis named ST215 is a common cause of prosthetic joint infections and other deep surgical site infections in Northern Europe, but is not present elsewhere. The increasing resistance among S. epidermidis strains is a global concern. We used whole-genome sequencing to characterize ST215 from healthcare settings.

resultsWe completed the genome of a ST215 isolate from a Swedish hospital using short and long reads, resulting in a circular 2,676,787 bp chromosome and a 2,326 bp plasmid. The new ST215 genome was placed in phylogenetic context using 1,361 finished public S. epidermidis reference genomes. We generated 10 additional short-read ST215 genomes and 11 short-read genomes of ST2, which is another common multidrug-resistant lineage at the same hospital. We studied recombination's role in the evolution of ST2 and ST215, and found multiple recombination events averaging 30-50 kb. By comparing the results of antimicrobial susceptibility testing for 31 antimicrobial drugs with the genome content encoding antimicrobial resistance in the ST215 and ST2 isolates, we found highly similar resistance traits between the isolates, with 22 resistance genes being shared between all the ST215 and ST2 genomes. The ST215 genome contained 29 genes that were historically identified as virulence genes of S. epidermidis ST2. We established that in the nucleotide sequence stretches identified as recombination events, virulence genes were overrepresented in ST215, while antibiotic resistance genes were overrepresented in ST2.

conclusionsThis study features the extensive antibiotic resistance and virulence gene content in ST215 genomes. ST215 and ST2 lineages have similarly evolved, acquiring resistance and virulence through genomic recombination. The results highlight the threat of new multidrug-resistant S. epidermidis lineages emerging in healthcare settings.

Indexed as

Anti-Bacterial AgentsCross InfectionDrug Resistance, Multiple, BacterialGenome, BacterialPhylogenyStaphylococcal InfectionsStaphylococcus epidermidisWhole Genome SequencingHumansMicrobial Sensitivity TestsPlasmidsRecombination, GeneticSwedenAnti-Bacterial AgentsCross infection/epidemiologyDrug resistance, multiple, bacterial multidrug resistanceHealthcare-associated infectionsStaphylococcus epidermidisWhole-genome sequencing

Identifiers

PMID38890594
PMCPMC11186124

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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.