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ID 65237
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Fujimori, Takumi Microbiology Division, Clinical Laboratory, Okayama University Hospital
Hagiya, Hideharu Department of General Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences ORCID Kaken ID researchmap
Iio, Koji Microbiology Division, Clinical Laboratory, Okayama University Hospital
Yamasaki, Osamu Department of Dermatology, Shimane University Faculty of Medicine
Miyamoto, Yuji Department of Mycobacteriology, Leprosy Research Center, National Institute of Infectious Diseases
Hoshino, Yoshihiko Department of Mycobacteriology, Leprosy Research Center, National Institute of Infectious Diseases
Kakehi, Ayaka Microbiology Division, Clinical Laboratory, Okayama University Hospital
Okura, Mami Microbiology Division, Clinical Laboratory, Okayama University Hospital
Minabe, Hiroshi Microbiology Division, Clinical Laboratory, Okayama University Hospital
Yokoyama, Yukika Microbiology Division, Clinical Laboratory, Okayama University Hospital
Otsuka, Fumio Department of General Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences ORCID Kaken ID publons researchmap
Higashikage, Akihito Microbiology Division, Clinical Laboratory, Okayama University Hospital
Abstract
Buruli ulcer is the third most common mycobacterial infection worldwide and is mainly diagnosed in tropical regions. Globally, this progressive disease is caused by Mycobacterium ulcerans; however, Mycobacterium ulcerans subsp. shinshuense, an Asian variant, has been exclusively identified in Japan. Because of insufficient clinical cases, the clinical features of M. ulcerans subsp. shinshuense–associated Buruli ulcer remain unclear. A 70-year-old Japanese woman presented with erythema on her left backhand. The skin lesion deteriorated without an apparent etiology of inflammation, and she was referred to our hospital 3 months after disease onset. A biopsy specimen was incubated in 2% Ogawa medium at 30 °C. After 66 days, we detected small yellow-pigmented colonies, suggesting scotochromogens. Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI Biotyper; Bruker Daltonics, Billerica, MA, USA) indicated that the organism was Mycobacterium pseudoshottsii or Mycobacterium marinum. However, additional PCR testing for the insertion sequence 2404 (IS2404) was positive, suggesting that the pathogen was either M. ulcerans or M. ulcerans subsp. shinshuense. Further examination by 16S rRNA sequencing analysis, focusing on nucleotide positions 492, 1247, 1288, and 1449–1451, we finally identified the organism as M. ulcerans subsp. shinshuense. The patient was successfully treated with 12 weeks of clarithromycin and levofloxacin treatment. Mass spectrometry is the latest microbial diagnostic method; however, it cannot be used to identify M. ulcerans subsp. shinshuense. To accurately detect this enigmatic pathogen and uncover its epidemiology and clinical characteristics in Japan, more accumulation of clinical cases with accurate identification of the causative pathogen is essential.
Keywords
Buruli ulcer
Mycobacterium ulcerans
Mycobacterium ulcerans subsp
shinshuense
16S rRNA sequencing analysis
Note
© 2023 Japanese Society of Chemotherapy and The Japanese Association for Infectious Diseases. This manuscript version is made available under the CC-BY-NC-ND 4.0 License. http://creativecommons.org/licenses/by-nc-nd/4.0/. This is the accepted manuscript version. The formal published version is available at https://doi.org/10.1016/j.jiac.2023.02.009.
This fulltext file will be available in May 2024.
Published Date
2023-05
Publication Title
Journal of Infection and Chemotherapy
Volume
volume29
Issue
issue5
Publisher
Elsevier BV
Start Page
523
End Page
526
ISSN
1341-321X
NCID
AA11057978
Content Type
Journal Article
language
English
OAI-PMH Set
岡山大学
Copyright Holders
© 2023 Japanese Society of Chemotherapy and The Japanese Association for Infectious Diseases.
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isVersionOf https://doi.org/10.1016/j.jiac.2023.02.009
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http://creativecommons.org/licenses/by-nc-nd/4.0/