Metagenomic Next-Generation Sequencing of Plasma for Diagnosis of COVID-19-Associated Pulmonary Aspergillosis

Timely diagnosis remains an unmet need in non-neutropenic patients at risk for aspergillosis, including those with COVID-19-associated pulmonary aspergillosis (CAPA), which in its early stages is characterized by tissue-invasive growth of the lungs with limited angioinvasion. Currently available myc...

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Published in:Journal of clinical microbiology Vol. 61; no. 3; p. e0185922
Main Authors: Hoenigl, Martin, Egger, Matthias, Price, Jessica, Krause, Robert, Prattes, Juergen, White, P Lewis
Format: Journal Article
Language:English
Published: United States American Society for Microbiology 23-03-2023
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Summary:Timely diagnosis remains an unmet need in non-neutropenic patients at risk for aspergillosis, including those with COVID-19-associated pulmonary aspergillosis (CAPA), which in its early stages is characterized by tissue-invasive growth of the lungs with limited angioinvasion. Currently available mycological tests show limited sensitivity when testing blood specimens. Metagenomic next-generation sequencing (mNGS) to detect microbial cell-free DNA (mcfDNA) in plasma might overcome some of the limitations of conventional diagnostics. A two-center cohort study involving 114 COVID-19 intensive care unit patients evaluated the performance of plasma mcfDNA sequencing for the diagnosis of CAPA. Classification of CAPA was performed using the European Confederation for Medical Mycology (ECMM)/International Society for Human and Animal Mycoses (ISHAM) criteria. A total of 218 plasma samples were collected between April 2020 and June 2021 and tested for mcfDNA (Karius test). Only 6 patients were classified as probable CAPA, and 2 were classified as possible, while 106 patients did not fulfill CAPA criteria. The Karius test detected DNA of mold pathogens in 12 samples from 8 patients, including Aspergillus fumigatus in 10 samples from 6 patients. Mold pathogen DNA was detected in 5 of 6 (83% sensitivity) cases with probable CAPA (A. fumigatus in 8 samples from 4 patients and Rhizopus microsporus in 1 sample), while the test did not detect molds in 103 of 106 (97% specificity) cases without CAPA. The Karius test showed promising performance for diagnosis of CAPA when testing plasma, being highly specific. The test detected molds in all but one patient with probable CAPA, including cases where other mycological tests from blood resulted continuously negative, outlining the need for validation in larger studies.
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Martin Hoenigl and Matthias Egger contributed equally to this article. Author order was determined by the corresponding author after negotiation.
The authors declare a conflict of interest. M.H. received research funding from Gilead, Astellas, MSD, Euroimmune, Scynexis, F2G and Pfizer. P.L.W. performed diagnostic evaluations and received meeting sponsorship from Bruker, Dynamiker, and Launch Diagnostics; Speakers fees, expert advice fees and meeting sponsorship from Gilead; Speaker and expert advice fees from F2G and speaker fees MSD and Pfizer; Speakers fees and performed diagnostic evaluations for Associates of Cape Cod and IMMY. Juergen Prattes received research funding from MSD and Pfizer outside of the work. All other authors declare no conflict of interest for this study.
Juergen Prattes and P. Lewis White contributed equally to this article. Author order was determined by the corresponding author after negotiation.
ISSN:0095-1137
1098-660X
DOI:10.1128/jcm.01859-22