Investigation of a Legionnaires’ Disease Outbreak in Yamagata City, Japan, 2019, Using Direct Sequence-Based Typing

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Published inJapanese Journal of Infectious Diseases Vol. 74; no. 5; pp. 491 - 494
Main Authors Seto, Junji, Amemura-Maekawa, Junko, Sampei, Mika, Araki, Kyoko, Endo, Misao, Kura, Fumiaki, Ikeda, Tatsuya, Kato, Takeo, Ohnishi, Makoto, Mizuta, Katsumi
Format Journal Article
LanguageEnglish
Published Tokyo National Institute of Infectious Diseases, Japanese Journal of Infectious Diseases Editorial Committee 30.09.2021
Japan Science and Technology Agency
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ArticleNumber JJID.2020.815
Author Araki, Kyoko
Kato, Takeo
Endo, Misao
Ohnishi, Makoto
Kura, Fumiaki
Ikeda, Tatsuya
Amemura-Maekawa, Junko
Seto, Junji
Sampei, Mika
Mizuta, Katsumi
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  fullname: Seto, Junji
  organization: Department of Microbiology, Yamagata Prefectural Institute of Public Health, Japan
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  fullname: Amemura-Maekawa, Junko
  organization: Department of Bacteriology I, National Institute of Infectious Diseases, Japan
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  fullname: Sampei, Mika
  organization: Department of Microbiology, Yamagata Prefectural Institute of Public Health, Japan
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  organization: Yamagata City Institute of Public Health, Japan
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  fullname: Endo, Misao
  organization: Yamagata City Institute of Public Health, Japan
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  fullname: Kura, Fumiaki
  organization: Department of Bacteriology I, National Institute of Infectious Diseases, Japan
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  fullname: Ikeda, Tatsuya
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  fullname: Ohnishi, Makoto
  organization: Department of Bacteriology I, National Institute of Infectious Diseases, Japan
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  fullname: Mizuta, Katsumi
  organization: Department of Microbiology, Yamagata Prefectural Institute of Public Health, Japan
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10.1099/jmm.0.000257
10.1128/AEM.00721-18
10.1128/JCM.00261-07
10.1128/JCM.43.5.2047-2052.2005
10.1007/s10096-011-1535-0
10.1016/S0140-6736(15)60078-2
10.11150/kansenshogakuzasshi1970.67.1062
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References 3. Chang B, Amemura-Maekawa J, Watanabe H. An improved protocol for the preparation and restriction enzyme digestion of pulsed-field gel electrophoresis agarose plugs for the analysis of Legionella isolates. Jpn J Infect Dis. 2009;62:54-6.
1. Cunha BA, Burillo A, Bouza E. Legionnaires' disease. Lancet. 2016;387:376-85.
4. Gaia V, Fry NK, Afshar B, et al. Consensus sequence-based scheme for epidemiological typing of clinical and environmental isolates of Legionella pneumophila. J Clin Microbiol. 2005;43:2047-52.
8. Koide M, Saito A, Higa F, et al. Study of Legionella pneumophila detection by two step polymerase chain reaction. Kansenshogaku Zasshi. 1993;67:1062-7. Japanese.
5. Ratzow S, Gaia V, Helbig JH, et al. Addition of neuA, the gene encoding N-acylneuraminate cytidylyl transferase, increases the discriminatory ability of the consensus sequence-based scheme for typing Legionella pneumophila serogroup 1 strains. J Clin Microbiol. 2007;45:1965-8.
9. Mahbubani MH, Bej AK, Miller R, et al. Detection of Legionella with polymerase chain reaction and gene probe methods. Mol Cell Probes. 1990;4:175-87.
2. Amemura-Maekawa J, Kura F, Chida K, et al. Legionella pneumophila and other Legionella species isolated from legionellosis patients in Japan between 2008 and 2016. Appl Environ Microbiol. 2018;84:e00721-18.
10. Mentasti M, Afshar B, Collins S, et al. Rapid investigation of cases and clusters of Legionnaires' disease in England and Wales using direct molecular typing. J Med Microbiol. 2016;65:484-93.
6. National Institute of Infectious Diseases. Laboratory manuals for pathogen detection, legionellosis. Available at <https://www.niid.go.jp/niid/images/lab-manual/Legionella20200904.pdf>. Accessed December 10, 2020. Japanese.
11. Annaka T. Rapid and simple detection of Legionella species by LAMP, a new DNA amplification method. Rinsho Biseibutshu Jinsoku Shindan Kenkyukai Shi. 2003;14:25-30. Japanese.
7. Mentasti M, Fry NK, Afshar B, et al. Application of Legionella pneumophila-specific quantitative real-time PCR combined with direct amplification and sequence-based typing in the diagnosis and epidemiological investigation of Legionnaires' disease. Eur J Clin Microbiol. 2012;31:2017-28.
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References_xml – reference: 3. Chang B, Amemura-Maekawa J, Watanabe H. An improved protocol for the preparation and restriction enzyme digestion of pulsed-field gel electrophoresis agarose plugs for the analysis of Legionella isolates. Jpn J Infect Dis. 2009;62:54-6.
– reference: 8. Koide M, Saito A, Higa F, et al. Study of Legionella pneumophila detection by two step polymerase chain reaction. Kansenshogaku Zasshi. 1993;67:1062-7. Japanese.
– reference: 9. Mahbubani MH, Bej AK, Miller R, et al. Detection of Legionella with polymerase chain reaction and gene probe methods. Mol Cell Probes. 1990;4:175-87.
– reference: 4. Gaia V, Fry NK, Afshar B, et al. Consensus sequence-based scheme for epidemiological typing of clinical and environmental isolates of Legionella pneumophila. J Clin Microbiol. 2005;43:2047-52.
– reference: 6. National Institute of Infectious Diseases. Laboratory manuals for pathogen detection, legionellosis. Available at <https://www.niid.go.jp/niid/images/lab-manual/Legionella20200904.pdf>. Accessed December 10, 2020. Japanese.
– reference: 10. Mentasti M, Afshar B, Collins S, et al. Rapid investigation of cases and clusters of Legionnaires' disease in England and Wales using direct molecular typing. J Med Microbiol. 2016;65:484-93.
– reference: 2. Amemura-Maekawa J, Kura F, Chida K, et al. Legionella pneumophila and other Legionella species isolated from legionellosis patients in Japan between 2008 and 2016. Appl Environ Microbiol. 2018;84:e00721-18.
– reference: 7. Mentasti M, Fry NK, Afshar B, et al. Application of Legionella pneumophila-specific quantitative real-time PCR combined with direct amplification and sequence-based typing in the diagnosis and epidemiological investigation of Legionnaires' disease. Eur J Clin Microbiol. 2012;31:2017-28.
– reference: 11. Annaka T. Rapid and simple detection of Legionella species by LAMP, a new DNA amplification method. Rinsho Biseibutshu Jinsoku Shindan Kenkyukai Shi. 2003;14:25-30. Japanese.
– reference: 5. Ratzow S, Gaia V, Helbig JH, et al. Addition of neuA, the gene encoding N-acylneuraminate cytidylyl transferase, increases the discriminatory ability of the consensus sequence-based scheme for typing Legionella pneumophila serogroup 1 strains. J Clin Microbiol. 2007;45:1965-8.
– reference: 1. Cunha BA, Burillo A, Bouza E. Legionnaires' disease. Lancet. 2016;387:376-85.
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SubjectTerms Legionella pneumophila
Legionnaire's disease
pulsed-field gel electrophoresis
respiratory specimen
SBT
sequence-based typing
Title Investigation of a Legionnaires’ Disease Outbreak in Yamagata City, Japan, 2019, Using Direct Sequence-Based Typing
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