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Volume 31, Number 3—March 2025
Etymologia

Tsukamurella tyrosinosolvens (tsū-kə-mə-rel′lə tī′-rǝ-sē-nō-sol′vins)

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Author affiliation: Emory University School of Medicine, Atlanta, Georgia, USA

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Gram staining from aerobic blood cultures (×1,000 magnification) showing numerous long, slightly curved, thin, nonbranching, and gram-positive rods, confirmed as Tsukamurella tyrosinosolvens. Image from (2); licensed by CC by 4.0 (https://creativecommons.org/licenses/by/4.0).

Figure. Gram staining from aerobic blood cultures (×1,000 magnification) showing numerous long, slightly curved, thin, nonbranching, and gram-positive rods, confirmed as Tsukamurella tyrosinosolvens. Image from (2); licensed...

The species name for the bacterium Tsukamurella tyrosinosolvens was accepted in 1997 on the basis of biochemical attributes: tyrosina, from the amino acid tyrosine in cheese (tyros, Greek for cheese), which imparts a crystalline texture (Figure). The hydrolysis, or dissolving of tyrosine—thus, tyrosinosolvens—is a species characteristic.

The genus Tsukamurella consists of commensal bacteria with a propensity to cause opportunistic infections in immunocompromised patients, especially those with chronic lung disease. Tsukamurella bacteria are related to the genera Nocardia, Mycobacterium, Corynebacterium, and Gordonia. Gordonia aurantiaca was initially isolated in 1971 by renowned Japanese physician-microbiologist and Mycobacteria taxonomist Michio Tsukamura at Nagoya University in Nagoya, Japan. In 1988, he was honored with the genus name Tsukamurella.

Tsukamurella, retrospectively isolated by Edward A. Steinhaus in 1941 from the mycetoma and ovaries of the bedbug, was originally misidentified as Corynebacterium paurometabolum. Tsukamurella are weakly acid-fast; therefore, clinical manifestations can be confused with those of tuberculosis and create microbiological misidentification with Mycobacterium and Corynebacterium spp.

Tsukamurella infections are rare and usually associated with immune-suppressed patients, but severe infections have occurred in immunocompetent patients. Currently, of 17 known species, 12 cause human disease. Although Tsukamurella infections have been increasingly reported in Europe, Asia, America, and Africa, T. tyrosinosolvens has been the most common species observed.

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References

  1. Genus Tsukamurella. LPSN—List of Prokaryotic names with Standing in Nomenclature [cited 2024 Dec 27]. https://lpsn.dsmz.de/genus/tsukamurella
  2. Mizuno  S, Tsukamura  Y, Nishio  S, Ishida  T, Hasegawa  D, Kosaka  Y, et al. Catheter-related bloodstream infection caused by Tsukamurella tyrosinosolvens identified by secA1sequencing in an immunocompromised child: a case report. Ann Clin Microbiol Antimicrob. 2023;22:97. DOIPubMedGoogle Scholar
  3. Species Tsukamurella tyrosinosolvens. LPSN—List of Prokaryotic names with Standing in Nomenclature [cited 2024 Dec 27]. https://lpsn.dsmz.de/species/tsukamurella-tyrosinosolvens
  4. Steinhaus  EA. A study of the bacteria associated with thirty species of insects. J Bacteriol. 1941;42:75790. DOIPubMedGoogle Scholar
  5. Teng  JLL, Tang  Y, Wong  SSY, Fong  JYH, Zhao  Z, Wong  C-P, et al. MALDI-TOF MS for identification of Tsukamurella species: Tsukamurella tyrosinosolvens as the predominant species associated with ocular infections. Emerg Microbes Infect. 2018;7:80. DOIPubMedGoogle Scholar
  6. Usuda  D, Tanaka  R, Suzuki  M, Shimozawa  S, Takano  H, Hotchi  Y, et al. Obligate aerobic, gram-positive, weak acid-fast, nonmotile bacilli, Tsukamurella tyrosinosolvens: Minireview of a rare opportunistic pathogen. World J Clin Cases. 2022;10:84439. DOIPubMedGoogle Scholar
  7. Yu  S, Ding  X, Hua  K, Zhu  H, Zhang  Q, Song  X, et al. Systematic investigation of the emerging pathogen of Tsukamurella species in a Chinese tertiary teaching hospital. Microbiol Spectr. 2023;11:e0164423. DOIPubMedGoogle Scholar

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Suggested citation for this article: Partin C. Tsukamurella tyrosinosolvens (tsū-kə-mə-rel′lə tīʹ-rō-sē-nō-sel′vins). Emerg Infect Dis. 2025 Mar [date cited]. https://doi.org/10.3201/eid3103.242004

DOI: 10.3201/eid3103.242004

Original Publication Date: February 21, 2025

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Clyde Partin, Emory Clinic, 1365 Clifton Rd NE, Bldg A, 1st Fl, Atlanta, GA 30322, USA

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Page created: February 04, 2025
Page updated: February 21, 2025
Page reviewed: February 21, 2025
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
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