Multiple Cases of Cutaneous Mycobacterium massiliense Infection in a “Hot Spa” in Japan
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Published in | Journal of Clinical Microbiology Vol. 49; no. 2; pp. 613 - 617 |
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AbstractList | Seven body polishers working in the same “hot spa” presented with multiple red nodules and papules on their hands and forearms. A causative agent was successfully isolated from two of the subjects and from a swab sample collected from the underside of a bed cover in the body-polishing facility. The two cutaneous isolates and the environmental isolate were rapidly growing mycobacteria that formed nonphotochromogenic smooth or smooth/rough colonies on Ogawa egg slants. They were identified as
Mycobacterium massiliense
by multigenotypic analysis using the 16S rRNA,
hsp65
, and
rpoB
genes and the 16S–23S rRNA internal transcribed spacer (ITS) region. However, the use of the 16S rRNA gene sequence and/or DNA-DNA hybridization (DDH Mycobacteria Kit) alone would not distinguish
M. massiliense
from mycobacteria in the
M. chelonae-M. abscessus
group. The three isolates were significantly more susceptible to clarithromycin, doxycycline, and minocycline than the
M. abscessus
and
M. bolletii
reference strains. One cutaneous isolate and the environmental isolate were in a related cluster by randomly amplified polymorphic DNA PCR (RAPD-PCR). Of the several mycobacterial species found in the day spa, only
M. massiliense
was isolated from biopsy specimens of the skin lesions, suggesting that this bacterium is a human skin pathogen. This is the first known report of cutaneous
M. massiliense
infections that could not be attributed to a prior invasive procedure. This is also the first report of
M. massiliense
infection in Japan. Seven body polishers working in the same "hot spa" presented with multiple red nodules and papules on their hands and forearms. A causative agent was successfully isolated from two of the subjects and from a swab sample collected from the underside of a bed cover in the body-polishing facility. The two cutaneous isolates and the environmental isolate were rapidly growing mycobacteria that formed nonphotochromogenic smooth or smooth/rough colonies on Ogawa egg slants. They were identified as Mycobacterium massiliense by multigenotypic analysis using the 16S rRNA, hsp65, and rpoB genes and the 16S-23S rRNA internal transcribed spacer (ITS) region. However, the use of the 16S rRNA gene sequence and/or DNA-DNA hybridization (DDH Mycobacteria Kit) alone would not distinguish M. massiliense from mycobacteria in the M. chelonae-M. abscessus group. The three isolates were significantly more susceptible to clarithromycin, doxycycline, and minocycline than the M. abscessus and M. bolletii reference strains. One cutaneous isolate and the environmental isolate were in a related cluster by randomly amplified polymorphic DNA PCR (RAPD-PCR). Of the several mycobacterial species found in the day spa, only M. massiliense was isolated from biopsy specimens of the skin lesions, suggesting that this bacterium is a human skin pathogen. This is the first known report of cutaneous M. massiliense infections that could not be attributed to a prior invasive procedure. This is also the first report of M. massiliense infection in Japan.Seven body polishers working in the same "hot spa" presented with multiple red nodules and papules on their hands and forearms. A causative agent was successfully isolated from two of the subjects and from a swab sample collected from the underside of a bed cover in the body-polishing facility. The two cutaneous isolates and the environmental isolate were rapidly growing mycobacteria that formed nonphotochromogenic smooth or smooth/rough colonies on Ogawa egg slants. They were identified as Mycobacterium massiliense by multigenotypic analysis using the 16S rRNA, hsp65, and rpoB genes and the 16S-23S rRNA internal transcribed spacer (ITS) region. However, the use of the 16S rRNA gene sequence and/or DNA-DNA hybridization (DDH Mycobacteria Kit) alone would not distinguish M. massiliense from mycobacteria in the M. chelonae-M. abscessus group. The three isolates were significantly more susceptible to clarithromycin, doxycycline, and minocycline than the M. abscessus and M. bolletii reference strains. One cutaneous isolate and the environmental isolate were in a related cluster by randomly amplified polymorphic DNA PCR (RAPD-PCR). Of the several mycobacterial species found in the day spa, only M. massiliense was isolated from biopsy specimens of the skin lesions, suggesting that this bacterium is a human skin pathogen. This is the first known report of cutaneous M. massiliense infections that could not be attributed to a prior invasive procedure. This is also the first report of M. massiliense infection in Japan. Seven body polishers working in the same "hot spa" presented with multiple red nodules and papules on their hands and forearms. A causative agent was successfully isolated from two of the subjects and from a swab sample collected from the underside of a bed cover in the body-polishing facility. The two cutaneous isolates and the environmental isolate were rapidly growing mycobacteria that formed nonphotochromogenic smooth or smooth/rough colonies on Ogawa egg slants. They were identified as Mycobacterium massiliense by multigenotypic analysis using the 16S rRNA, hsp65, and rpoB genes and the 16S-23S rRNA internal transcribed spacer (ITS) region. However, the use of the 16S rRNA gene sequence and/or DNA-DNA hybridization (DDH Mycobacteria Kit) alone would not distinguish M. massiliense from mycobacteria in the M. chelonae-M. abscessus group. The three isolates were significantly more susceptible to clarithromycin, doxycycline, and minocycline than the M. abscessus and M. bolletii reference strains. One cutaneous isolate and the environmental isolate were in a related cluster by randomly amplified polymorphic DNA PCR (RAPD-PCR). Of the several mycobacterial species found in the day spa, only M. massiliense was isolated from biopsy specimens of the skin lesions, suggesting that this bacterium is a human skin pathogen. This is the first known report of cutaneous M. massiliense infections that could not be attributed to a prior invasive procedure. This is also the first report of M. massiliense infection in Japan. Article Usage Stats Services JCM Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit StumbleUpon Twitter current issue JCM About JCM Subscribers Authors Reviewers Advertisers Inquiries from the Press Permissions & Commercial Reprints ASM Journals Public Access Policy JCM RSS Feeds 1752 N Street N.W. • Washington DC 20036 202.737.3600 • 202.942.9355 fax • journals@asmusa.org Print ISSN: 0095-1137 Online ISSN: 1098-660X Copyright © 2014 by the American Society for Microbiology. For an alternate route to JCM .asm.org, visit: JCM |
Author | Atsuko Tomita Yuko Era Masanari Furuta Masahiko Makino Yoshihiko Hoshino Motohisa Washizu Kentaro Matsumoto Norihisa Ishii Yuji Kanazawa Kazue Nakanaga |
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References | e_1_3_2_26_2 e_1_3_2_20_2 e_1_3_2_21_2 e_1_3_2_22_2 e_1_3_2_23_2 e_1_3_2_24_2 e_1_3_2_25_2 e_1_3_2_9_2 e_1_3_2_15_2 e_1_3_2_8_2 e_1_3_2_16_2 e_1_3_2_7_2 e_1_3_2_17_2 e_1_3_2_6_2 e_1_3_2_18_2 e_1_3_2_19_2 e_1_3_2_10_2 e_1_3_2_5_2 e_1_3_2_11_2 e_1_3_2_12_2 e_1_3_2_3_2 e_1_3_2_13_2 e_1_3_2_2_2 e_1_3_2_14_2 Della-Latta P. (e_1_3_2_4_2) 1998 19403765 - J Clin Microbiol. 2009 Jul;47(7):2149-55 19850725 - Nucleic Acids Res. 2010 Jan;38(Database issue):D33-8 19846643 - J Clin Microbiol. 2009 Dec;47(12):4124-8 17409204 - J Clin Microbiol. 2007 Jun;45(6):1978-80 17881555 - J Clin Microbiol. 2007 Nov;45(11):3840-3 9431937 - J Clin Microbiol. 1998 Jan;36(1):139-47 19515839 - J Clin Microbiol. 2009 Aug;47(8):2596-600 18507923 - Emerg Infect Dis. 2008 Jun;14(6):984-5 15583272 - J Clin Microbiol. 2004 Dec;42(12):5493-501 18753344 - J Clin Microbiol. 2008 Oct;46(10):3384-90 20536733 - Microbiol Immunol. 2010 Jun;54(6):347-53 18950729 - Microbes Infect. 2008 Nov-Dec;10(14-15):1552-7 17488738 - Mol Biol Evol. 2007 Aug;24(8):1596-9 8381805 - J Clin Microbiol. 1993 Feb;31(2):175-8 19571015 - J Clin Microbiol. 2009 Sep;47(9):2691-8 19420162 - J Clin Microbiol. 2009 Jul;47(7):1985-95 1761680 - J Clin Microbiol. 1991 Aug;29(8):1596-603 9399508 - J Clin Microbiol. 1997 Dec;35(12):3132-9 17626174 - J Clin Microbiol. 2007 Sep;45(9):3127-30 19732795 - J Infect. 2009 Nov;59(5):324-31 18174307 - J Clin Microbiol. 2008 Mar;46(3):850-5 17989199 - J Clin Microbiol. 2008 Jan;46(1):69-72 8727884 - J Clin Microbiol. 1996 May;34(5):1100-7 |
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Mendeley... Seven body polishers working in the same “hot spa” presented with multiple red nodules and papules on their hands and forearms. A causative agent was... Seven body polishers working in the same "hot spa" presented with multiple red nodules and papules on their hands and forearms. A causative agent was... |
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SubjectTerms | Anti-Bacterial Agents - pharmacology Bacterial Proteins - genetics Bacterial Typing Techniques Biological and medical sciences Cluster Analysis DNA, Bacterial - chemistry DNA, Bacterial - genetics DNA, Ribosomal - chemistry DNA, Ribosomal - genetics Environmental Microbiology Female Fundamental and applied biological sciences. Psychology Humans Japan Microbial Sensitivity Tests Microbiology Middle Aged Molecular Sequence Data Mycobacteriology and Aerobic Actinomycetes Mycobacterium Mycobacterium - classification Mycobacterium - genetics Mycobacterium - isolation & purification Mycobacterium Infections - diagnosis Mycobacterium Infections - microbiology Nucleic Acid Hybridization Random Amplified Polymorphic DNA Technique RNA, Ribosomal, 16S - genetics Sequence Analysis, DNA Skin Diseases, Bacterial - diagnosis Skin Diseases, Bacterial - microbiology |
Title | Multiple Cases of Cutaneous Mycobacterium massiliense Infection in a “Hot Spa” in Japan |
URI | http://jcm.asm.org/content/49/2/613.abstract https://www.ncbi.nlm.nih.gov/pubmed/21159943 https://www.proquest.com/docview/850559846 https://www.proquest.com/docview/907151113 https://www.proquest.com/docview/907157995 https://pubmed.ncbi.nlm.nih.gov/PMC3043493 |
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