%0 Journal Article
%T Rapid multiplex real-time PCR assay using a portable device for the detection of oral pathogens.
%A Wint WY
%A Miyanohara M
%A Yamada H
%A Nakatsuka T
%A Okamoto M
%A Ryo K
%A Tanaka T
%A Hanada N
%A Murata T
%J Diagn Microbiol Infect Dis
%V 109
%N 1
%D 2024 May 15
%M 38402755
%F 2.983
%R 10.1016/j.diagmicrobio.2024.116214
%X 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.