Evidence map›Paper›PMID 38273191›Full record

ArticleEuropean journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology2024

Predicting the primary infection source of Escherichia coli bacteremia using virulence-associated genes.

Christian Schaadt Ilsby, Frederik Boetius Hertz, Henrik Westh, Jonathan Monk, Peder Worning, Helle Krogh Johansen, Katrine Hartung Hansen, Mette Pinholt

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In one paragraph

Article in European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 99% 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

1 citing paper in PubMed, 0 citations in OpenAlex.

  1. 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 at 3 institutions in 2 countries.

Christian Schaadt IlsbyDepartment of Clinical Microbiology, Copenhagen University Hospital Hvidovre, Hvidovre, Denmark. chr.ilsby@gmail.com.ORCID http://orcid.org/0000-0002-9029-203X
Frederik Boetius HertzDepartment of Clinical Microbiology, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.
Henrik WesthDepartment of Clinical Microbiology, Copenhagen University Hospital Hvidovre, Hvidovre, Denmark.
Jonathan MonkDepartment of Bioengineering, University of California, San Diego, CA, USA.
Peder WorningDepartment of Clinical Microbiology, Copenhagen University Hospital Hvidovre, Hvidovre, Denmark.
Helle Krogh JohansenDepartment of Clinical Microbiology, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.
Katrine Hartung HansenDepartment of Clinical Microbiology, Copenhagen University Hospital Hvidovre, Hvidovre, Denmark.
Mette PinholtDepartment of Clinical Microbiology, Copenhagen University Hospital Hvidovre, Hvidovre, Denmark.
University of Copenhagen · DKHvidovre Hospital · DKUniversity of California San Diego · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo investigate the role of E. coli virulence-associated genes (VAGs) in predicting urinary tract infection (UTI) as the source of bacteremia in two distinct hospital populations, one with a large general catchment area and one dominated by referrals.

methodsE. coli bacteremias identified at Department of Clinical Microbiology (DCM), Hvidovre Hospital and DCM, Rigshospitalet in the Capital Region of Denmark from October to December 2018. Using whole genome sequencing (WGS), we identified 358 VAGs from 224 E. coli bacteremia. For predictive analysis, VAGs were paired with clinical source of UTI from local bacteremia databases.

resultsVAGs strongly predicting of UTI as primary infection source of bacteremia were primarily found within the pap gene family. papX (PPV 96%, sensitivity 54%) and papGII (PPV 93%, sensitivity 56%) were found highly predictive, but showed low sensitivities. The strength of VAG predictions of UTI as source varied significantly between the two hospital populations. VAGs had weaker predictions in the tertiary referral center (Rigshospitalet), a disparity likely stemming from differences in patient population and department specialization.

conclusionWGS data was used to predict the primary source of E. coli bacteremia and is an attempt on a new and different type of infection source identification. Genomic data showed potential to be utilized to predict the primary source of infection; however, discrepancy between the best performing profile of VAGs between acute care hospitals and tertiary hospitals makes it difficult to implement in clinical practice.

Indexed as

BacteremiaEscherichia coli InfectionsEscherichia coli ProteinsUrinary Tract InfectionsEscherichia coliHumansVirulenceVirulence FactorsEscherichia coli ProteinsVirulence FactorsBacteremiaE. coliUrosepsisVirulence-associated genesWGS

Identifiers

PMID38273191
PMCPMC10965582
OpenAlexW4391213404

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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.