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Identification of invasive fungal diseases in immunocompromised patients by combining an Aspergillus specific PCR with a multifungal DNA-microarray from primary clinical samples.
Boch, T; Reinwald, M; Postina, P; Cornely, O A; Vehreschild, J J; Heußel, C P; Heinz, W J; Hoenigl, M; Eigl, S; Lehrnbecher, T; Hahn, J; Claus, B; Lauten, M; Egerer, G; Müller, M C; Will, S; Merker, N; Hofmann, W-K; Buchheidt, D; Spiess, B.
Affiliation
  • Boch T; Department of Hematology and Oncology, University Hospital Mannheim, University of Heidelberg, Mannheim, Germany.
  • Reinwald M; Department of Hematology and Oncology, University Hospital Mannheim, University of Heidelberg, Mannheim, Germany.
  • Postina P; Department of Hematology and Oncology, University Hospital Mannheim, University of Heidelberg, Mannheim, Germany.
  • Cornely OA; Department I of Internal Medicine, University Hospital of Cologne, Cologne, Germany.
  • Vehreschild JJ; Clinical Trials Centre Cologne, ZKS Köln, BMBF 01KN1106, Centre for Integrated Oncology CIO Köln Bonn, Cologne, Germany.
  • Heußel CP; Cologne Excellence Cluster on Cellular Stress Response in Aging-Associated Diseases (CECAD), University of Cologne, Cologne, Germany.
  • Heinz WJ; Department I of Internal Medicine, University Hospital of Cologne, Cologne, Germany.
  • Hoenigl M; German Centre for Infection Research, Partner site Bonn-Cologne, Cologne, Germany.
  • Eigl S; Department of Diagnostic and Interventional Radiology with Nuclear Medicine, Thoraxklinik at Heidelberg University Hospital, Heidelberg, Germany.
  • Lehrnbecher T; Department II of Internal Medicine, Würzburg University Hospital, Würzburg, Germany.
  • Hahn J; Section of Infectious Diseases and Tropical Medicine and Division of Pulmonology, Medical University of Graz, Graz, Austria.
  • Claus B; Section of Infectious Diseases and Tropical Medicine and Division of Pulmonology, Medical University of Graz, Graz, Austria.
  • Lauten M; Pediatric Hematology and Oncology, Children's Hospital, University of Frankfurt, Frankfurt, Germany.
  • Egerer G; Regensburg University Hospital, Regensburg, Germany.
  • Müller MC; Ludwigshafen General Hospital, Ludwigshafen, Germany.
  • Will S; Department of Pediatrics, University Hospital Schleswig-Holstein, Campus Lübeck, Lübeck, Germany.
  • Merker N; Department V of Internal Medicine, University Hospital Heidelberg, Heidelberg, Germany.
  • Hofmann WK; Department of Hematology and Oncology, University Hospital Mannheim, University of Heidelberg, Mannheim, Germany.
  • Buchheidt D; Department of Hematology and Oncology, University Hospital Mannheim, University of Heidelberg, Mannheim, Germany.
  • Spiess B; Department of Hematology and Oncology, University Hospital Mannheim, University of Heidelberg, Mannheim, Germany.
Mycoses ; 58(12): 735-45, 2015 Dec.
Article in En | MEDLINE | ID: mdl-26497302
ABSTRACT
The increasing incidence of invasive fungal diseases (IFD), most of all invasive aspergillosis (IA) in immunocompromised patients emphasises the need to improve the diagnostic tools for detection of fungal pathogens. We investigated the diagnostic performance of a multifungal DNA-microarray detecting 15 different fungi [Aspergillus, Candida, Fusarium, Mucor, Rhizopus, Scedosporium and Trichosporon species (spp.)] in addition to an Aspergillus specific polymerase chain reaction (PCR) assay. Biopsies, bronchoalveolar lavage and peripheral blood samples of 133 immunocompromised patients (pts) were investigated by a multifungal DNA-microarray as well as a nested Aspergillus specific PCR assay. Patients had proven (n = 18), probable (n = 29), possible (n = 48) and no IFD (n = 38) and were mostly under antifungal therapy at the time of sampling. The results were compared to culture, histopathology, imaging and serology, respectively. For the non-Aspergillus IFD the microarray analysis yielded in all samples a sensitivity of 64% and a specificity of 80%. Best results for the detection of all IFD were achieved by combining DNA-microarray and Aspergillus specific PCR in biopsy samples (sensitivity 79%; specificity 71%). The molecular assays in combination identify genomic DNA of fungal pathogens and may improve identification of causative pathogens of IFD and help overcoming the diagnostic uncertainty of culture and/or histopathology findings, even during antifungal therapy.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Aspergillosis / Aspergillus fumigatus / Oligonucleotide Array Sequence Analysis / Multiplex Polymerase Chain Reaction Type of study: Clinical_trials / Diagnostic_studies / Evaluation_studies / Prognostic_studies Limits: Adult / Female / Humans / Male Language: En Journal: Mycoses Year: 2015 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Aspergillosis / Aspergillus fumigatus / Oligonucleotide Array Sequence Analysis / Multiplex Polymerase Chain Reaction Type of study: Clinical_trials / Diagnostic_studies / Evaluation_studies / Prognostic_studies Limits: Adult / Female / Humans / Male Language: En Journal: Mycoses Year: 2015 Document type: Article