Retrospective analysis of 300 microbial cell-free DNA sequencing results in routine blood stream infection diagnostics

IntroductionBloodstream infections are a critical challenge worldwide due to the slow turnaround time of conventional microbiological tests for detecting bacteremia in septic patients. Noscendo GmbH (Duisburg, Germany) has developed the CE/IVD pipeline DISQVER for clinical metagenomics testing based...

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Main Authors: Claudio Neidhöfer, Niklas Klein, Aylin Yürüktümen, Tessa Hattenhauer, Rebekka Mispelbaum, Christian Bode, Tobias A. W. Holderried, Achim Hoerauf, Marijo Parčina
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-01-01
Series:Frontiers in Cellular and Infection Microbiology
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Online Access:https://www.frontiersin.org/articles/10.3389/fcimb.2025.1504262/full
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author Claudio Neidhöfer
Claudio Neidhöfer
Niklas Klein
Niklas Klein
Aylin Yürüktümen
Tessa Hattenhauer
Rebekka Mispelbaum
Christian Bode
Tobias A. W. Holderried
Achim Hoerauf
Marijo Parčina
author_facet Claudio Neidhöfer
Claudio Neidhöfer
Niklas Klein
Niklas Klein
Aylin Yürüktümen
Tessa Hattenhauer
Rebekka Mispelbaum
Christian Bode
Tobias A. W. Holderried
Achim Hoerauf
Marijo Parčina
author_sort Claudio Neidhöfer
collection DOAJ
description IntroductionBloodstream infections are a critical challenge worldwide due to the slow turnaround time of conventional microbiological tests for detecting bacteremia in septic patients. Noscendo GmbH (Duisburg, Germany) has developed the CE/IVD pipeline DISQVER for clinical metagenomics testing based on cell-free DNA (cfDNA) from blood samples to address this issue.MethodsWe conducted a retrospective study to evaluate the diagnostic utility of this methodological setup in improving treatment decisions since it was introduced into our clinical setting. Between January 2021 and June 2022, the first 300 cases in which DISQVER was applied at our university hospital were collected and analyzed. The results were compared with routine microbiology test results, clinical picture, associated treatment decisions, and clinical course.ResultsOur findings demonstrate that DISQVER results where no pathogen was reported effectively ruled out bacterial bloodstream infections, whereas positive results varied in their usefulness. While the metagenomic approach proved highly valuable for detecting non-culturable and rare pathogens, its utility was limited in cases where detected microorganisms were commonly associated with the microbiota.DiscussionPerforming on-site analysis might mitigate delays resulting from logistical challenges and might help optimizing antibiotic stewardship. Once prompt results can be obtained, the relevance of incorporating molecular resistograms will become more pronounced. Further, the specific patient subgroups that most benefit from this analysis must be worked out. Guiding clinicians in identifying the infection focus based on the detected bacteria would significantly improve patient care. Lastly, evidence of filamentous fungi must be diligently followed up.
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publishDate 2025-01-01
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spelling doaj-art-cf21c4c514da4570a4312b26ebc82de92025-01-30T06:22:39ZengFrontiers Media S.A.Frontiers in Cellular and Infection Microbiology2235-29882025-01-011510.3389/fcimb.2025.15042621504262Retrospective analysis of 300 microbial cell-free DNA sequencing results in routine blood stream infection diagnosticsClaudio Neidhöfer0Claudio Neidhöfer1Niklas Klein2Niklas Klein3Aylin Yürüktümen4Tessa Hattenhauer5Rebekka Mispelbaum6Christian Bode7Tobias A. W. Holderried8Achim Hoerauf9Marijo Parčina10Institute of Experimental Hematology and Transfusion Medicine, University Hospital Bonn, Bonn, GermanyInstitute of Medical Microbiology, Immunology and Parasitology, University Hospital Bonn, Bonn, GermanyInstitute of Medical Microbiology, Immunology and Parasitology, University Hospital Bonn, Bonn, GermanyDepartment of Microbiology and Hospital Hygiene, Bundeswehr Central Hospital Koblenz, Koblenz, GermanyDepartment of Internal Medicine II, University Hospital Bonn, Bonn, GermanyDepartment of Hematology, Oncology, Stem Cell Transplantation, Immune and Cell Therapy, Clinical Immunology and Rheumatology, University Hospital Bonn, Bonn, GermanyDepartment of Hematology, Oncology, Stem Cell Transplantation, Immune and Cell Therapy, Clinical Immunology and Rheumatology, University Hospital Bonn, Bonn, GermanyDepartment of Anesthesiology and Intensive Care Medicine, University Hospital Bonn, Bonn, GermanyDepartment of Hematology, Oncology, Stem Cell Transplantation, Immune and Cell Therapy, Clinical Immunology and Rheumatology, University Hospital Bonn, Bonn, GermanyInstitute of Medical Microbiology, Immunology and Parasitology, University Hospital Bonn, Bonn, GermanyInstitute of Medical Microbiology, Immunology and Parasitology, University Hospital Bonn, Bonn, GermanyIntroductionBloodstream infections are a critical challenge worldwide due to the slow turnaround time of conventional microbiological tests for detecting bacteremia in septic patients. Noscendo GmbH (Duisburg, Germany) has developed the CE/IVD pipeline DISQVER for clinical metagenomics testing based on cell-free DNA (cfDNA) from blood samples to address this issue.MethodsWe conducted a retrospective study to evaluate the diagnostic utility of this methodological setup in improving treatment decisions since it was introduced into our clinical setting. Between January 2021 and June 2022, the first 300 cases in which DISQVER was applied at our university hospital were collected and analyzed. The results were compared with routine microbiology test results, clinical picture, associated treatment decisions, and clinical course.ResultsOur findings demonstrate that DISQVER results where no pathogen was reported effectively ruled out bacterial bloodstream infections, whereas positive results varied in their usefulness. While the metagenomic approach proved highly valuable for detecting non-culturable and rare pathogens, its utility was limited in cases where detected microorganisms were commonly associated with the microbiota.DiscussionPerforming on-site analysis might mitigate delays resulting from logistical challenges and might help optimizing antibiotic stewardship. Once prompt results can be obtained, the relevance of incorporating molecular resistograms will become more pronounced. Further, the specific patient subgroups that most benefit from this analysis must be worked out. Guiding clinicians in identifying the infection focus based on the detected bacteria would significantly improve patient care. Lastly, evidence of filamentous fungi must be diligently followed up.https://www.frontiersin.org/articles/10.3389/fcimb.2025.1504262/fullsepsisbacteremiablood culturemolecular diagnostic techniquesnext generation sequencingclinical metagenomics
spellingShingle Claudio Neidhöfer
Claudio Neidhöfer
Niklas Klein
Niklas Klein
Aylin Yürüktümen
Tessa Hattenhauer
Rebekka Mispelbaum
Christian Bode
Tobias A. W. Holderried
Achim Hoerauf
Marijo Parčina
Retrospective analysis of 300 microbial cell-free DNA sequencing results in routine blood stream infection diagnostics
Frontiers in Cellular and Infection Microbiology
sepsis
bacteremia
blood culture
molecular diagnostic techniques
next generation sequencing
clinical metagenomics
title Retrospective analysis of 300 microbial cell-free DNA sequencing results in routine blood stream infection diagnostics
title_full Retrospective analysis of 300 microbial cell-free DNA sequencing results in routine blood stream infection diagnostics
title_fullStr Retrospective analysis of 300 microbial cell-free DNA sequencing results in routine blood stream infection diagnostics
title_full_unstemmed Retrospective analysis of 300 microbial cell-free DNA sequencing results in routine blood stream infection diagnostics
title_short Retrospective analysis of 300 microbial cell-free DNA sequencing results in routine blood stream infection diagnostics
title_sort retrospective analysis of 300 microbial cell free dna sequencing results in routine blood stream infection diagnostics
topic sepsis
bacteremia
blood culture
molecular diagnostic techniques
next generation sequencing
clinical metagenomics
url https://www.frontiersin.org/articles/10.3389/fcimb.2025.1504262/full
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