Abstract

This study developed a new method for forensic saliva identification using three oral bacteria, Streptococcus salivarius, Streptococcus sanguinis, and Neisseria subflava, combined with a real-time polymerase chain reaction (RT-PCR) system we called OB mRT-PCR. Analytical sensitivity results showed that the target bacteria were amplified at 102–107 copies/reaction, and analytical specificity was assessed using 24 other viruses, bacteria, and protozoa. To evaluate the OB mRT-PCR kit for forensic applications, saliva from 140 Korean individuals was tested, and at least two target bacteria were detected in all the samples. Additional studies on non-saliva samples demonstrated the specificity of the kit. Comparison of the kit with two conventional saliva test methods, the SALIgAE and RSID-Saliva assays, indicated that it was more sensitive and applicable to saliva samples in long-term storage (up to 14 weeks). Additionally, through amplification of mock forensic items and old DNA samples (isolated without lysis of the bacterial cells, regardless of their Gram-positivity), we found that the kit was applicable to not only saliva swabs, but also DNA samples. We suggest that this simple RT-PCR-based experimental method is feasible for rapid on-site analysis, and we expect this kit to be useful for saliva detection in old forensic DNA samples.

Details

Title
Rapid oral bacteria detection based on real-time PCR for the forensic identification of saliva
Author
Jung, Ju Yeon 1 ; Yoon, Hyun Kyu 2 ; An, Sanghyun 3 ; Lee, Jee Won 1   VIAFID ORCID Logo  ; Eu-Ree Ahn 1 ; Yeon-Ji, Kim 1 ; Park, Hyun-Chul 1 ; Lee, Kyungmyung 1 ; Jung Ho Hwang 1 ; Si-Keun Lim 1 

 Forensic DNA Division, National Forensic Service, Gangwon-do, Republic of Korea 
 JS Biotech, Business Incubation Center, Kyungbok University, Gyeonggi-do, Republic of Korea 
 DNA Analysis Division, Seoul Institute, National Forensic Service, Yangcheon-gu, Seoul, Republic of Korea 
Pages
1-10
Publication year
2018
Publication date
Jul 2018
Publisher
Nature Publishing Group
e-ISSN
20452322
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2071553250
Copyright
© 2018. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.