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 showe...
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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. |
doi_str_mv | 10.1038/s41598-018-29264-2 |
format | Article |
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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.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-018-29264-2</identifier><identifier>PMID: 30022122</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>45/77 ; 631/326 ; 631/337 ; Bacteria ; Deoxyribonucleic acid ; DNA ; DNA fingerprints ; Experimental methods ; Forensic science ; Genetic testing ; Humanities and Social Sciences ; Lysis ; multidisciplinary ; Polymerase chain reaction ; Protozoa ; Saliva ; Science ; Science (multidisciplinary)</subject><ispartof>Scientific reports, 2018-07, Vol.8 (1), p.10852-10, Article 10852</ispartof><rights>The Author(s) 2018</rights><rights>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.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c540t-efb16822c3db012649e0ef9b5516ecc1fc42a61ebe0431bd92a7c63de8cad3df3</citedby><cites>FETCH-LOGICAL-c540t-efb16822c3db012649e0ef9b5516ecc1fc42a61ebe0431bd92a7c63de8cad3df3</cites><orcidid>0000-0002-1865-3865</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6052055/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6052055/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,41096,42165,51551,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30022122$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jung, Ju Yeon</creatorcontrib><creatorcontrib>Yoon, Hyun Kyu</creatorcontrib><creatorcontrib>An, Sanghyun</creatorcontrib><creatorcontrib>Lee, Jee Won</creatorcontrib><creatorcontrib>Ahn, Eu-Ree</creatorcontrib><creatorcontrib>Kim, Yeon-Ji</creatorcontrib><creatorcontrib>Park, Hyun-Chul</creatorcontrib><creatorcontrib>Lee, Kyungmyung</creatorcontrib><creatorcontrib>Hwang, Jung Ho</creatorcontrib><creatorcontrib>Lim, Si-Keun</creatorcontrib><title>Rapid oral bacteria detection based on real-time PCR for the forensic identification of saliva</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><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.</description><subject>45/77</subject><subject>631/326</subject><subject>631/337</subject><subject>Bacteria</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA fingerprints</subject><subject>Experimental methods</subject><subject>Forensic science</subject><subject>Genetic testing</subject><subject>Humanities and Social Sciences</subject><subject>Lysis</subject><subject>multidisciplinary</subject><subject>Polymerase chain reaction</subject><subject>Protozoa</subject><subject>Saliva</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kV1LBCEUhiWKiuoPdBFCN91M6XGcZm6CWPqCoFjqNnH0WMbsuOls0L_PbWv7uMibI57nvPr6ErLL2SFnoj5KJZdNXTBeF9BAVRawQjaBlbIAAbD6Y79BdlJ6ZnlJaErerJMNwRgAB9gkD2M99ZaGqDvaajNg9JpaHNAMPvT5KGHu9jSi7orBT5DejsbUhUiHJ5xX7JM31FvsB--80R9jwdGkO_-qt8ma013Cnc-6Re7Pz-5Gl8X1zcXV6PS6MLJkQ4Gu5VUNYIRtGc9uGmTomlZKXqEx3JkSdMWxRVYK3toG9LGphMXaaCusE1vkZKE7nbUTtCa_JjtS0-gnOr6poL363en9k3oMr6rKn8KkzAIHnwIxvMwwDWrik8Gu0z2GWVLAjoHXoqpYRvf_oM9hFvtsb07xLAZyTsGCMjGkFNEtH8OZmieoFgmqnKD6SFBBHtr7aWM58pVXBsQCSLnVP2L8vvsf2XfytaeK</recordid><startdate>20180718</startdate><enddate>20180718</enddate><creator>Jung, Ju Yeon</creator><creator>Yoon, Hyun Kyu</creator><creator>An, Sanghyun</creator><creator>Lee, Jee Won</creator><creator>Ahn, Eu-Ree</creator><creator>Kim, Yeon-Ji</creator><creator>Park, Hyun-Chul</creator><creator>Lee, Kyungmyung</creator><creator>Hwang, Jung Ho</creator><creator>Lim, Si-Keun</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-1865-3865</orcidid></search><sort><creationdate>20180718</creationdate><title>Rapid oral bacteria detection based on real-time PCR for the forensic identification of saliva</title><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></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c540t-efb16822c3db012649e0ef9b5516ecc1fc42a61ebe0431bd92a7c63de8cad3df3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>45/77</topic><topic>631/326</topic><topic>631/337</topic><topic>Bacteria</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA fingerprints</topic><topic>Experimental methods</topic><topic>Forensic science</topic><topic>Genetic testing</topic><topic>Humanities and Social Sciences</topic><topic>Lysis</topic><topic>multidisciplinary</topic><topic>Polymerase chain reaction</topic><topic>Protozoa</topic><topic>Saliva</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jung, Ju Yeon</creatorcontrib><creatorcontrib>Yoon, Hyun Kyu</creatorcontrib><creatorcontrib>An, Sanghyun</creatorcontrib><creatorcontrib>Lee, Jee Won</creatorcontrib><creatorcontrib>Ahn, Eu-Ree</creatorcontrib><creatorcontrib>Kim, Yeon-Ji</creatorcontrib><creatorcontrib>Park, Hyun-Chul</creatorcontrib><creatorcontrib>Lee, Kyungmyung</creatorcontrib><creatorcontrib>Hwang, Jung Ho</creatorcontrib><creatorcontrib>Lim, Si-Keun</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jung, Ju Yeon</au><au>Yoon, Hyun Kyu</au><au>An, Sanghyun</au><au>Lee, Jee Won</au><au>Ahn, Eu-Ree</au><au>Kim, Yeon-Ji</au><au>Park, Hyun-Chul</au><au>Lee, Kyungmyung</au><au>Hwang, Jung Ho</au><au>Lim, Si-Keun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rapid oral bacteria detection based on real-time PCR for the forensic identification of saliva</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2018-07-18</date><risdate>2018</risdate><volume>8</volume><issue>1</issue><spage>10852</spage><epage>10</epage><pages>10852-10</pages><artnum>10852</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><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 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.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>30022122</pmid><doi>10.1038/s41598-018-29264-2</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-1865-3865</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 45/77 631/326 631/337 Bacteria Deoxyribonucleic acid DNA DNA fingerprints Experimental methods Forensic science Genetic testing Humanities and Social Sciences Lysis multidisciplinary Polymerase chain reaction Protozoa Saliva Science Science (multidisciplinary) |
title | Rapid oral bacteria detection based on real-time PCR for the forensic identification of saliva |
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