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

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.

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Publication Details

Journal
npj Genomic Medicine
Published
2025-03-17
DOI
https://doi.org/10.1038/s41525-025-00482-8
Citations
5
Primary Topic
Antifungal resistance and susceptibility
Type
article
Field-Weighted Citation Impact
6.98

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article

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

Myrthe Jager, Tom F.W. Wolfs, Laura G.Y. Rotte, Carlo Vermeulen et al.
5 citations
npj Genomic Medicine
Antifungal resistance and susceptibility
6.98
article

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

Myrthe Jager, Tom F.W. Wolfs, Laura G.Y. Rotte, Carlo Vermeulen, Louis Bont, Emmy Wesdorp, Caroline A. Lindemans, Nicolle Besselink, Jeroen de Ridder, Ferry Hagen, Tjomme van der Bruggen, Li‐Ting Chen
article en
5 citations

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.

npj Genomic MedicineVol. 10(1)
University Medical Center Utrecht (NL), Oncode Institute (NL), Westerdijk Fungal Biodiversity Institute (NL), Princess Máxima Center (NL), Wilhelmina Children's Hospital (NL), University of Amsterdam (NL)
Nederlandse Organisatie voor Wetenschappelijk Onderzoek
Life in Land
Openalex Percentile: Top 3%
Antifungal resistance and susceptibility
6.98
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