Rapid multiplex real-time PCR assay using a portable device for the detection of oral pathogens

被引:0
|
作者
Wint, Wit Yee [1 ]
Miyanohara, Mayu [1 ]
Yamada, Hidenori [1 ]
Nakatsuka, Takako [1 ]
Okamoto, Masaaki [1 ]
Ryo, Koufuchi [1 ]
Tanaka, Tomoko [2 ]
Hanada, Nobuhiro [1 ,3 ]
Murata, Takatoshi [1 ]
机构
[1] Tsurumi Univ, Sch Dent Med, Dept Oral Hlth Sci, Tsurumi, Yokohama 2308501, Japan
[2] Nippon Dent Univ Tokyo, Sch Life Dent Tokyo, Dept Oral Hlth, Fujimi,Chiyoda Ku, Tokyo 1028159, Japan
[3] Univ Shanghai Sci & Technol, Inst Photochem & Photocatalyst, Shanghai, Peoples R China
基金
日本学术振兴会;
关键词
Multiplex real-time PCR; Oral pathogen; Portable device; Saliva; POLYMERASE-CHAIN-REACTION; QUANTITATIVE DETECTION; TREPONEMA-DENTICOLA; GENOME SEQUENCE; PCR1100;
D O I
10.1016/j.diagmicrobio.2024.116214
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Colonization by several oral pathogens and the onset of oral diseases, such as dental caries and periodontal diseases, are closely related. Therefore, the analysis of pathogens in oral specimens would be helpful for the risk assessment of oral diseases. We developed a rapid multiplex real-time polymerase chain reaction (PCR) method using a portable device and newly designed probe/primer sets to detect the oral pathogens Streptococcus mutans, Porphyromonas gingivalis, Treponema denticola, and Tannerella forsythia. The theoretical minimum detectable cell numbers of S. mutans, P. gingivalis, T. denticola, and T. forsythia were 1, 1, 4, and 3, respectively. The multiplex real-time PCR system simultaneously detected the colonization of S. mutans and P. gingivalis in human saliva. These results suggest that the multiplex real-time PCR system may be useful for the risk assessment of oral diseases.
引用
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页数:7
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