Evidence map›Paper›PMID 31166888›Full record

ArticleMicrobial genomics2019

Enterococcus faecium genome dynamics during long-term asymptomatic patient gut colonization.

Jumamurat R Bayjanov, Jery Baan, Malbert R C Rogers, Annet Troelstra, Rob J L Willems, Willem van Schaik

Open access · goldAbstract read
In one paragraph

Article in Microbial genomics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

30 citing papers in PubMed, 39 citations in OpenAlex.

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  16. Review
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  18. Interactions between commensalFEMS microbes · 2024
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  19. Review
  20. 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

6 authors at 1 institution in 2 countries.

Jumamurat R BayjanovDepartment of Medical Microbiology, University Medical Center Utrecht, 3584CX Utrecht, The Netherlands.
Jery BaanDepartment of Medical Microbiology, University Medical Center Utrecht, 3584CX Utrecht, The Netherlands.
Malbert R C RogersDepartment of Medical Microbiology, University Medical Center Utrecht, 3584CX Utrecht, The Netherlands.
Annet TroelstraDepartment of Medical Microbiology, University Medical Center Utrecht, 3584CX Utrecht, The Netherlands.
Rob J L WillemsDepartment of Medical Microbiology, University Medical Center Utrecht, 3584CX Utrecht, The Netherlands.
Willem van SchaikInstitute of Microbiology and Infection, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK.
University Medical Center Utrecht · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Enterococcus faecium is a gut commensal of humans and animals. In addition, it has recently emerged as an important nosocomial pathogen through the acquisition of genetic elements that confer resistance to antibiotics and virulence. We performed a whole-genome sequencing-based study on 96 multidrug-resistant E. faecium strains that asymptomatically colonized five patients with the aim of describing the genome dynamics of this species. The patients were hospitalized on multiple occasions and isolates were collected over periods ranging from 15 months to 6.5 years. Ninety-five of the sequenced isolates belonged to E. faecium clade A1, which was previously determined to be responsible for the vast majority of clinical infections. The clade A1 strains clustered into six clonal groups of highly similar isolates, three of which consisted entirely of isolates from a single patient. We also found evidence of concurrent colonization of patients by multiple distinct lineages and transfer of strains between patients during hospitalization. We estimated the evolutionary rate of two clonal groups that each colonized single patients at 12.6 and 25.2 single-nucleotide polymorphisms (SNPs)/genome/year. A detailed analysis of the accessory genome of one of the clonal groups revealed considerable variation due to gene gain and loss events, including the chromosomal acquisition of a 37 kbp prophage and the loss of an element containing carbohydrate metabolism-related genes. We determined the presence and location of 12 different insertion sequence (IS) elements, with ISEfa5 showing a unique pattern of location in 24 of the 25 isolates, suggesting widespread ISEfa5 excision and insertion into the genome during gut colonization. Our findings show that the E. faecium genome is highly dynamic during asymptomatic colonization of the human gut. We observed considerable genomic flexibility due to frequent horizontal gene transfer and recombination, which can contribute to the generation of genetic diversity within the species and, ultimately, can contribute to its success as a nosocomial pathogen.

Indexed as

Cross InfectionDNA, BacterialDNA Transposable ElementsDrug Resistance, MicrobialEnterococcus faeciumEvolution, MolecularGastrointestinal MicrobiomeGenome, BacterialGram-Positive Bacterial InfectionsHumansRecombination, GeneticDNA, BacterialDNA Transposable Elementsaccessory genomeEnterococcus faeciumgut colonizationinsertion sequencesmicrobial evolution

Identifiers

PMID31166888
PMCPMC6700664
OpenAlexW2950991961

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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.