Identification of causative fungus from sterile abscess using metagenomics followed by in situ hybridization

Author:

Oki Hiroya12ORCID,Niwa Ryotaro34,Pranee Somboonthum5,Motooka Daisuke261ORCID,Onda Yoshiyuki74,Nakata Jun8ORCID,Nakajima Hiroko9,Oka Yoshihiro1011,Sugiyama Haruo9,Yoshii Yuka1,Anzai Naoyuki4,Nakamura Shota612,Iida Tetsuya52

Affiliation:

1. NGS Core Facility, Research Institute for Microbial Diseases (RIMD), Osaka University, Osaka, Japan

2. Department of Infection Metagenomics, Research Institute for Microbial Diseases (RIMD), Osaka University, Osaka, Japan

3. Department of Hematology, Yodogawa Christian Hospital, Osaka, Japan

4. Department of Hematology and Oncology, Takatsuki Red Cross Hospital, Osaka, Japan

5. Department of Bacterial Infections, Research Institute for Microbial Diseases (RIMD), Osaka University, Osaka, Japan

6. Institute for Open and Transdisciplinary Research Initiatives (OTRI), Integrated Frontier Research for Medical Science Division (iFremed), Osaka University, Osaka, Japan

7. Department of Hematology and Oncology, Osaka Red Cross Hospital, Osaka, Japan

8. Department of Clinical Laboratory and Biomedical Sciences, Graduate School of Medicine, Osaka University, Osaka, Japan

9. Department of Cancer Immunology, Graduate School of Medicine, Osaka University, Osaka, Japan

10. Department of Immunopathology, Immunology Frontier Research Center (World Premier International Research Center), Osaka University, Osaka, Japan

11. Department of Cancer Stem Cell Biology, Graduate School of Medicine, Osaka University, Osaka, Japan

Abstract

Introduction. Invasive fungal infections require early diagnosis for treatment. Microscopic observation of biopsy and blood culture is the gold standard for the identification of the causative fungus, but it is difficult to identify the causative pathogen by a sterile abscess biopsy. Case Presentation. We present a case report of breakthrough invasive trichosporonosis in a 65-year-old Japanese male with acute myeloid leukaemia receiving antifungal prophylaxis. Blood cultures showed no fungal growth, and a liver biopsy and a removed spleen with abscess showed fragmented fungi, but no fungal identification was possible. This report demonstrates that retrospective analyses were able to identify the causative fungus. Conclusion. We narrowed down the candidate fungi by deep sequencing of the ITS1 region of fungal genome and confirmed that the fungus observed in the specimen was Trichosporon asahii by in situ hybridization using a DNA probe targeting 26S rRNA.

Funder

JSPS

Publisher

Microbiology Society

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