Evidence map›Paper›PMID 38323373›Full record

ArticleThe Journal of antimicrobial chemotherapy2024

Consideration of within-patient diversity highlights transmission pathways and antimicrobial resistance gene variability in vancomycin-resistant Enterococcus faecium.

Martin P McHugh, Kerry A Pettigrew, Surabhi Taori, Thomas J Evans, Alistair Leanord, Stephen H Gillespie, Kate E Templeton, Matthew T G Holden

Abstract read
In one paragraph

Article in The Journal of antimicrobial chemotherapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Co-carriage of diverse vancomycin-resistantJAC-antimicrobial resistance · 2025
    Article
  5. Article
  6. Article
  7. Deciphering vancomycin resistance inFrontiers 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

8 authors.

Martin P McHughSchool of Medicine, University of St Andrews, St Andrews, UK.ORCID 0000-0002-0370-3700
Kerry A PettigrewSchool of Medicine, University of St Andrews, St Andrews, UK.
Surabhi TaoriMedical Microbiology, Department of Laboratory Medicine, Royal Infirmary of Edinburgh, Edinburgh, UK.
Thomas J EvansSchool of Infection and Immunity, University of Glasgow, Glasgow, UK.ORCID 0000-0002-4140-6352
Alistair LeanordSchool of Infection and Immunity, University of Glasgow, Glasgow, UK.
Stephen H GillespieSchool of Medicine, University of St Andrews, St Andrews, UK.
Kate E TempletonMedical Microbiology, Department of Laboratory Medicine, Royal Infirmary of Edinburgh, Edinburgh, UK.
Matthew T G HoldenSchool of Medicine, University of St Andrews, St Andrews, UK.ORCID 0000-0002-4958-2166

Funding

Chief Scientist OfficeWellcome Trust
6 · The paper itself

Abstract

backgroundWGS is increasingly being applied to healthcare-associated vancomycin-resistant Enterococcus faecium (VREfm) outbreaks. Within-patient diversity could complicate transmission resolution if single colonies are sequenced from identified cases.

objectivesDetermine the impact of within-patient diversity on transmission resolution of VREfm. MATERIALS AND

methodsFourteen colonies were collected from VREfm positive rectal screens, single colonies were collected from clinical samples and Illumina WGS was performed. Two isolates were selected for Oxford Nanopore sequencing and hybrid genome assembly to generate lineage-specific reference genomes. Mapping to closely related references was used to identify genetic variations and closely related genomes. A transmission network was inferred for the entire genome set using Phyloscanner. RESULTS AND DISCUSSION: In total, 229 isolates from 11 patients were sequenced. Carriage of two or three sequence types was detected in 27% of patients. Presence of antimicrobial resistance genes and plasmids was variable within genomes from the same patient and sequence type. We identified two dominant sequence types (ST80 and ST1424), with two putative transmission clusters of two patients within ST80, and a single cluster of six patients within ST1424. We found transmission resolution was impaired using fewer than 14 colonies.

conclusionsPatients can carry multiple sequence types of VREfm, and even within related lineages the presence of mobile genetic elements and antimicrobial resistance genes can vary. VREfm within-patient diversity could be considered in future to aid accurate resolution of transmission networks.

Indexed as

Anti-Infective AgentsEnterococcus faeciumAnti-Bacterial AgentsDrug Resistance, BacterialHumansVancomycinAnti-Bacterial AgentsAnti-Infective AgentsVancomycin

Identifiers

PMID38323373
PMCPMC11090465

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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.