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Rapid oral bacteria detection based on real-time PCR for the forensic identification of saliva

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 t...

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Autores principales: Jung, Ju Yeon, Yoon, Hyun Kyu, An, Sanghyun, Lee, Jee Won, Ahn, Eu-Ree, Kim, Yeon-Ji, Park, Hyun-Chul, Lee, Kyungmyung, Hwang, Jung Ho, Lim, Si-Keun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6052055/
https://www.ncbi.nlm.nih.gov/pubmed/30022122
http://dx.doi.org/10.1038/s41598-018-29264-2
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author Jung, Ju Yeon
Yoon, Hyun Kyu
An, Sanghyun
Lee, Jee Won
Ahn, Eu-Ree
Kim, Yeon-Ji
Park, Hyun-Chul
Lee, Kyungmyung
Hwang, Jung Ho
Lim, Si-Keun
author_facet Jung, Ju Yeon
Yoon, Hyun Kyu
An, Sanghyun
Lee, Jee Won
Ahn, Eu-Ree
Kim, Yeon-Ji
Park, Hyun-Chul
Lee, Kyungmyung
Hwang, Jung Ho
Lim, Si-Keun
author_sort Jung, Ju Yeon
collection PubMed
description 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 10(2)–10(7) 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.
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spelling pubmed-60520552018-07-23 Rapid oral bacteria detection based on real-time PCR for the forensic identification of saliva Jung, Ju Yeon Yoon, Hyun Kyu An, Sanghyun Lee, Jee Won Ahn, Eu-Ree Kim, Yeon-Ji Park, Hyun-Chul Lee, Kyungmyung Hwang, Jung Ho Lim, Si-Keun Sci Rep Article 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 10(2)–10(7) 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. Nature Publishing Group UK 2018-07-18 /pmc/articles/PMC6052055/ /pubmed/30022122 http://dx.doi.org/10.1038/s41598-018-29264-2 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Jung, Ju Yeon
Yoon, Hyun Kyu
An, Sanghyun
Lee, Jee Won
Ahn, Eu-Ree
Kim, Yeon-Ji
Park, Hyun-Chul
Lee, Kyungmyung
Hwang, Jung Ho
Lim, Si-Keun
Rapid oral bacteria detection based on real-time PCR for the forensic identification of saliva
title Rapid oral bacteria detection based on real-time PCR for the forensic identification of saliva
title_full Rapid oral bacteria detection based on real-time PCR for the forensic identification of saliva
title_fullStr Rapid oral bacteria detection based on real-time PCR for the forensic identification of saliva
title_full_unstemmed Rapid oral bacteria detection based on real-time PCR for the forensic identification of saliva
title_short Rapid oral bacteria detection based on real-time PCR for the forensic identification of saliva
title_sort rapid oral bacteria detection based on real-time pcr for the forensic identification of saliva
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6052055/
https://www.ncbi.nlm.nih.gov/pubmed/30022122
http://dx.doi.org/10.1038/s41598-018-29264-2
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