4.5 Article

Assessment of panfungal PCR performance with formalin-fixed paraffin-embedded tissue specimens†

Journal

MEDICAL MYCOLOGY
Volume 60, Issue 2, Pages -

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/mmy/myac004

Keywords

panfungal PCR; formalin-fixed tissues; molecular mycology; quality improvement

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In this study, we evaluated the performance of a DNA-based test for detecting fungal DNA in archived human biopsy tissues. Our results indicate that the best performance can be achieved when fungi are observed under a microscope before testing, suggesting that this test should only be used under these conditions.
We reviewed the performance of a panfungal ITS-2 PCR and Sanger sequencing assay performed on 88 FFPE specimens at The Hospital for Sick Children (Toronto, Canada) in 2019. A potential fungal pathogen was identified by ITS PCR in 62.7 and 2.9% of positive and negative direct slide examination of tissue specimens, respectively. ITS amplicons were detected in 87/88 specimens, with 53/88 (60.2%) considered as 'positive-contaminants' and 34/88 (38.6%) as 'positive-potential pathogen' upon sequencing. Potential pathogens included Blastomyces dermatitidis (17.1%), Cryptococcus neoformans (17.1%), Histoplasma capsulatum (14.3%) and Mucormycetes (11.4%). Laboratories should only perform ITS PCR on FFPE tissues if fungal elements have been confirmed on histopathology slides. Lay summary In this study, we examined how well a DNA-based test could detect DNA from fungi in archived human biopsy tissues. The best performance was achieved if fungi were seen in the tissue under a microscope before being tested. Our results indicate that we should only use this test if these conditions are met.

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