New Primer Design for Identification of Oral rothia, Including R. aeria, Using Multiplex PCR
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- Tsuzukibashi Osamu
- Departments of Laboratory Medicine for Dentistry, Nihon University School of Dentistry at Matsudo, Matsudo, Chiba 271-8587, Japan
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- Uchibori Satoshi
- Departments of Crown Bridge Prosthodontics, Nihon University School of Dentistry at Matsudo, Matsudo, Chiba 271-8587, Japan
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- Shinozaki-Kuwahara Noriko
- Departments of Oral Microbiology, Nihon University School of Dentistry at Matsudo, Matsudo, Chiba 271-8587, Japan
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- Saito Masanori
- Departments of Oral Microbiology, Nihon University School of Dentistry at Matsudo, Matsudo, Chiba 271-8587, Japan
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- Kobayashi Taira
- Departments of Crown Bridge Prosthodontics, Nihon University School of Dentistry at Matsudo, Matsudo, Chiba 271-8587, Japan
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- Fukumoto Masahiko
- Departments of Laboratory Medicine for Dentistry, Nihon University School of Dentistry at Matsudo, Matsudo, Chiba 271-8587, Japan
書誌事項
- タイトル別名
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- <b>New Primer Design for Identification of Oral rothia, Including </b><b><i>R. aeria</i></b><b>, Using Multiplex PCR </b>
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We previously reported a primer design for the identification of oral Rothia dentocariosa and Rothia mucilaginosa, using multiplex polymerase chain reaction(PCR). There is only one report of Rothia aeria, which is capable of causing serious systemic infections, being detected in the mouths of healthy individuals. Thus, if R. aeria is part of the normal flora in the oral cavity, a suitable identification method is necessary to assess the veritable prevalence of Rothia species, including R. aeria, in the oral cavity. <br>In this study, five PCR primers were designed based on partial sequences of the 16S rDNA genes of the above-mentioned known oral rothia and R. aeria. These primers react to R. dentocariosa, R. mucilaginosa and R. aeria, respectively, and did not react to other nonoral rothia. Moreover, representative non-Rothia oral bacteria displayed negative reactions to these primers. These results indicate that these primers are useful for identifying R. dentocariosa, R. mucilaginosa and R. aeria. We also developed a simple multiplex PCR procedure using the five PCR primers designed in the present study as a rapid and reliable method of identifying known oral rothia and R. aeria.
収録刊行物
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- IJOMS
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IJOMS 12 (2), 85-89, 2013
日本大学松戸歯学部 口腔科学研究所
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詳細情報 詳細情報について
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- CRID
- 1390282680190885632
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- NII論文ID
- 130003386570
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- ISSN
- 21854254
- 13479733
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- 本文言語コード
- en
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- データソース種別
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- JaLC
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