Evidence map›Paper›PMID 40990924›Full record

ArticleMicrobial genomics2025

Nanopore adaptive sampling for bacterial identification from periprosthetic joint replacement tissue.

Teresa L Street, Philip Bejon, Laura Leach, Sarah Oakley, Bernadette C Young, Nicholas D Sanderson

Abstract read
In one paragraph

Article in Microbial genomics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Teresa L StreetNIHR Oxford Biomedical Research Centre, John Radcliffe Hospital, Oxford, UK.
Philip BejonModernising Medical Microbiology, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Laura LeachOxford University Hospitals NHS Trust, Oxford, UK.
Sarah OakleyOxford University Hospitals NHS Trust, Oxford, UK.
Bernadette C YoungNIHR Oxford Biomedical Research Centre, John Radcliffe Hospital, Oxford, UK.
Nicholas D SandersonNIHR Oxford Biomedical Research Centre, John Radcliffe Hospital, Oxford, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metagenomic approaches to the diagnosis of prosthetic joint infections promise more accurate and more rapid diagnosis. However, the high host DNA to bacterial DNA ratio is a challenge. Nanopore adaptive sampling (AS) can be used to preferentially sequence more of the infecting organism. Here, we evaluate AS using clinical samples from infected prosthetic joints to determine the absolute fold enrichment achieved. We found that AS achieved a range of 1.61- to 1.96-fold higher absolute fold enrichment for bacterial sequenced bases using AS over control pores. In this limited sample set, AS did not impact bacterial diagnosis overall but led to a modest increase in the bacterial sequence available without any obvious cost.

Indexed as

BacteriaJoint ProsthesisMetagenomicsNanoporesProsthesis-Related InfectionsDNA, BacterialHumansDNA, Bacterialadaptive samplingclinical metagenomicsdiagnosticsdirect from sample sequencingnanopore

Identifiers

PMID40990924
PMCPMC13293318

What OpenQuestion holds

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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.