Evidence map›Paper›PMID 40097415›Full record

ArticleNPJ genomic medicine2025

NGS-based Aspergillus detection in plasma and lung lavage of children with invasive pulmonary aspergillosis.

Emmy Wesdorp, Laura Rotte, Li-Ting Chen, Myrthe Jager, Nicolle Besselink, Carlo Vermeulen, Ferry Hagen, Tjomme van der Bruggen, Caroline Lindemans, Tom Wolfs and 2 more

Abstract read
In one paragraph

Article in NPJ genomic medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
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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

12 authors.

Emmy WesdorpCenter for Molecular Medicine, University Medical Center Utrecht, Utrecht, The Netherlands.ORCID http://orcid.org/0000-0001-6656-2151
Laura Rotte *Hematopoietic stem cell transplantation, Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Li-Ting Chen *Center for Molecular Medicine, University Medical Center Utrecht, Utrecht, The Netherlands.ORCID http://orcid.org/0000-0001-7956-5116
Myrthe Jager *Center for Molecular Medicine, University Medical Center Utrecht, Utrecht, The Netherlands.
Nicolle BesselinkCenter for Molecular Medicine, University Medical Center Utrecht, Utrecht, The Netherlands.
Carlo VermeulenCenter for Molecular Medicine, University Medical Center Utrecht, Utrecht, The Netherlands.
Ferry HagenWesterdijk Fungal Biodiversity Institute, Utrecht, The Netherlands.ORCID http://orcid.org/0000-0002-5622-1916
Tjomme van der BruggenDepartment of Medical Microbiology, University Medical Centre Utrecht, Utrecht, The Netherlands.
Caroline LindemansHematopoietic stem cell transplantation, Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Tom WolfsDepartment of Pediatric Infectious Diseases and Immunology, Wilhelmina Children's hospital, UMC Utrecht, Utrecht, The Netherlands.
Louis BontDepartment of Pediatric Infectious Diseases and Immunology, Wilhelmina Children's hospital, UMC Utrecht, Utrecht, The Netherlands. L.Bont@umcutrecht.nl.
Jeroen de RidderCenter for Molecular Medicine, University Medical Center Utrecht, Utrecht, The Netherlands. J.deRidder-4@umcutrecht.nl.ORCID http://orcid.org/0000-0002-0828-3477

Funding

Nederlandse Organisatie voor Wetenschappelijk Onderzoek (Netherlands Organisation for Scientific Research) 639.072.715
6 · The paper itself

Abstract

In immunocompromised pediatric patients, diagnosing invasive pulmonary aspergillosis (IPA) poses a significant challenge. Next-Generation Sequencing (NGS) shows promise for detecting fungal DNA but lacks standardization. This study aims to advance towards clinical evaluation of liquid biopsy NGS for Aspergillus detection, through an evaluation of wet-lab procedures and computational analysis. Our findings support using both CHM13v2.0 and GRCh38.p14 in host-read mapping to reduce fungal false-positives. We demonstrate the sensitivity of our custom kraken2 database, cRE.21, in detecting Aspergillus species. Additionally, cell-free DNA sequencing shows superior performance to whole-cell DNA sequencing by recovering higher fractions of fungal DNA in lung fluid (bronchoalveolar lavage [BAL] fluid) and plasma samples from pediatric patients with probable IPA. In a proof-of-principle, A. fumigatus was identified in 5 out of 7 BAL fluid samples and 3 out of 5 plasma samples. This optimized workflow can advance fungal-NGS research and represents a step towards enhancing diagnostic certainty by enabling more sensitive and accurate species-level diagnosis of IPA in immunocompromised patients.

Identifiers

PMID40097415
PMCPMC11914610

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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.