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Mycobiome analysis in fungal Infected formalin-fixed and paraffin-embedded tissues for identification of pathogenic fungi: A pilot study

Taebum Lee, Hee Young Na, Kyoung-Mee Kim, Hey Seung Lee, Sung-Hye Park, Ji-Young Choe, Kyoung Chan Choi, View ORCID ProfileSun-ju Byeon
doi: https://doi.org/10.1101/2020.04.19.045856
Taebum Lee
1Department of Pathology and Translational Genomics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea
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Hee Young Na
2Department of Pathology, Seoul National University Bundang Hospital, Gyeonggi-do, Korea
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Kyoung-Mee Kim
1Department of Pathology and Translational Genomics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea
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Hey Seung Lee
2Department of Pathology, Seoul National University Bundang Hospital, Gyeonggi-do, Korea
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Sung-Hye Park
3Department of Pathology, Seoul National University College of Medicine, Seoul, Korea
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Ji-Young Choe
4Department of Pathology, Hallym University Sacred Heart Hospital, Hallym University College of Medicine, Gyeonggi-do, Korea
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Kyoung Chan Choi
5Department of Pathology, Chuncheon Sacred Heart Hospital, Hallym University College of Medicine, Chuncheon, Korea
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Sun-ju Byeon
6Department of Pathology, Hallym University Dongtan Sacred Heart Hospital, Hallym University College of Medicine, Gyeonggi-do, Korea
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  • ORCID record for Sun-ju Byeon
  • For correspondence: byeonsunju@hallym.ac.kr
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ABSTRACT

Background Fungal organisms are frequently observed in surgical pathological diagnosis. In order to more accurately identify fungi in formalin-fixed and paraffin-embedded (FFPE) tissues, it is necessary to use genomic information. The purpose of our pilot study is to identify the factors to be considered for the identification of pathogenic fungi using mycobiome analysis in FFPE tissues.

Methods We selected 49 cases in five hospitals. In each case, FFPE tissue was cut into 50 µm and DNA was extracted. Multiplex PCR with four primers (ITS1, ITS2, ITS3 and ITS4) was performed. Multiplex sequencing was performed using MinION device according to the manufacturer’s protocol. Sequences of each case were searched using BLASTN with an ITS database from NCBI RefSeq Targeted Loci Project with default parameter.

Results A total of 2,526 DNA nucleotides were sequenced. We were able to identify 342 fungal nucleotides in 24 (49.0%, 24/49) cases. The median value of the detected fungal DNA per case was 3 (1Q: 1 and 3Q: 14.25). The 215 (62.87%) fungal DNA contained the entire region of ITS1 or ITS2. The remaining 127 fungal DNAs were identified as fungi using partial sequence of ITS1, ITS2, 5.8S, LSU or SSU.

Conclusion In conclusion, we have identified the possibility of finding pathogenic fungi through mycobiome analysis in fungal infected FFPE tissues using nanopore sequencing method. However, we have also found several limitations to be solved for further studies. If we develop a method to characterize pathogenic fungi in FFPE tissues in a follow-up study, we think it will help patients to use appropriate antifungal agents.

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

  • https://github.com/byun1114/mycobiome_1/

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. All rights reserved. No reuse allowed without permission.
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Posted April 19, 2020.
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Mycobiome analysis in fungal Infected formalin-fixed and paraffin-embedded tissues for identification of pathogenic fungi: A pilot study
Taebum Lee, Hee Young Na, Kyoung-Mee Kim, Hey Seung Lee, Sung-Hye Park, Ji-Young Choe, Kyoung Chan Choi, Sun-ju Byeon
bioRxiv 2020.04.19.045856; doi: https://doi.org/10.1101/2020.04.19.045856
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Mycobiome analysis in fungal Infected formalin-fixed and paraffin-embedded tissues for identification of pathogenic fungi: A pilot study
Taebum Lee, Hee Young Na, Kyoung-Mee Kim, Hey Seung Lee, Sung-Hye Park, Ji-Young Choe, Kyoung Chan Choi, Sun-ju Byeon
bioRxiv 2020.04.19.045856; doi: https://doi.org/10.1101/2020.04.19.045856

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