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Polymerase chain reaction with a primer pair in the 16S-23S rRNA spacer region for detection of Mycoplasma pulmonis in clinical isolates
https://repo.qst.go.jp/records/43306
https://repo.qst.go.jp/records/43306883d00a5-8296-4d87-8466-380979892095
Item type | 学術雑誌論文 / Journal Article(1) | |||||
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公開日 | 2003-12-18 | |||||
タイトル | ||||||
タイトル | Polymerase chain reaction with a primer pair in the 16S-23S rRNA spacer region for detection of Mycoplasma pulmonis in clinical isolates | |||||
言語 | ||||||
言語 | eng | |||||
資源タイプ | ||||||
資源タイプ識別子 | http://purl.org/coar/resource_type/c_6501 | |||||
資源タイプ | journal article | |||||
アクセス権 | ||||||
アクセス権 | metadata only access | |||||
アクセス権URI | http://purl.org/coar/access_right/c_14cb | |||||
著者 |
Omoe, Hiromi
× Omoe, Hiromi× Omoe, Katsuhiko× Matsushita, Satoru× Kobayashi, Hideki× Yamamoto, Koushi× 重茂 浩美× 松下 悟 |
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抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | To develop a diagnostic tool to identify Mycoplasma pulmonis (M. pulmonis) in clinical isolates, we developed a polymerase chain reaction (PCR) assay using primers specific for the 16S-23S rRNA intergenic spacer region (SR) of M. pulmonis. One pair of PCR primers reacted specifically with two reference strains of M. pulmonis tested and seven samples isolated from naturally infected rats. The primer pair did not produce PCR products of the correct size from any other rodent or human mycoplasmas or cellular DNA from rodent lung. Specificity of the PCR assay was confirmed by Southern blotting with probe specific for the SR of M. pulmonis. The PCR assay for detection of M. pulmonis established in this study is suitable for diagnosis of M. pulmonis infection in clinical cases. | |||||
書誌情報 |
Comparative Immunology, Microbiology & Infectious Diseases 巻 27, 号 2, p. 117-128, 発行日 2004 |
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ISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 0147-9571 |