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Duplex loop-mediated isothermal amplification assay for simultaneous detection of human and human male DNA
OBJECTIVE: Screening of human and human male DNA is necessary for forensic DNA analyses. Although quantitative real-time PCR (qPCR) is commonly used for detecting and quantifying these DNA targets, its use as a screening tool is time-consuming and labor-intensive. To streamline and simplify the scre...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10464483/ https://www.ncbi.nlm.nih.gov/pubmed/37608397 http://dx.doi.org/10.1186/s13104-023-06464-2 |
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author | Kubo, Seiji Niimi, Hideki Kitajima, Isao |
author_facet | Kubo, Seiji Niimi, Hideki Kitajima, Isao |
author_sort | Kubo, Seiji |
collection | PubMed |
description | OBJECTIVE: Screening of human and human male DNA is necessary for forensic DNA analyses. Although quantitative real-time PCR (qPCR) is commonly used for detecting and quantifying these DNA targets, its use as a screening tool is time-consuming and labor-intensive. To streamline and simplify the screening process, we aimed to develop a duplex loop-mediated isothermal amplification (LAMP) assay capable of simultaneously detecting human and human male DNA in a single tube. We assessed the duplex LAMP assay for forensic application. RESULTS: For our duplex LAMP assay, we have utilized two fluorescent probes with HEX and FAM fluorophores to specifically detect human and human male DNA, respectively. The HEX (human target) signal was detected from both the male and female DNA samples, and the FAM (male target) signal was detected from only the male DNA sample. This assay has a sensitivity of 10–1 pg of DNA for both targets. Additionally, we successfully detected the two targets in the DNA samples extracted from forensically relevant body fluids, including blood, saliva, semen, and vaginal secretions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13104-023-06464-2. |
format | Online Article Text |
id | pubmed-10464483 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-104644832023-08-30 Duplex loop-mediated isothermal amplification assay for simultaneous detection of human and human male DNA Kubo, Seiji Niimi, Hideki Kitajima, Isao BMC Res Notes Research Note OBJECTIVE: Screening of human and human male DNA is necessary for forensic DNA analyses. Although quantitative real-time PCR (qPCR) is commonly used for detecting and quantifying these DNA targets, its use as a screening tool is time-consuming and labor-intensive. To streamline and simplify the screening process, we aimed to develop a duplex loop-mediated isothermal amplification (LAMP) assay capable of simultaneously detecting human and human male DNA in a single tube. We assessed the duplex LAMP assay for forensic application. RESULTS: For our duplex LAMP assay, we have utilized two fluorescent probes with HEX and FAM fluorophores to specifically detect human and human male DNA, respectively. The HEX (human target) signal was detected from both the male and female DNA samples, and the FAM (male target) signal was detected from only the male DNA sample. This assay has a sensitivity of 10–1 pg of DNA for both targets. Additionally, we successfully detected the two targets in the DNA samples extracted from forensically relevant body fluids, including blood, saliva, semen, and vaginal secretions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13104-023-06464-2. BioMed Central 2023-08-22 /pmc/articles/PMC10464483/ /pubmed/37608397 http://dx.doi.org/10.1186/s13104-023-06464-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Note Kubo, Seiji Niimi, Hideki Kitajima, Isao Duplex loop-mediated isothermal amplification assay for simultaneous detection of human and human male DNA |
title | Duplex loop-mediated isothermal amplification assay for simultaneous detection of human and human male DNA |
title_full | Duplex loop-mediated isothermal amplification assay for simultaneous detection of human and human male DNA |
title_fullStr | Duplex loop-mediated isothermal amplification assay for simultaneous detection of human and human male DNA |
title_full_unstemmed | Duplex loop-mediated isothermal amplification assay for simultaneous detection of human and human male DNA |
title_short | Duplex loop-mediated isothermal amplification assay for simultaneous detection of human and human male DNA |
title_sort | duplex loop-mediated isothermal amplification assay for simultaneous detection of human and human male dna |
topic | Research Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10464483/ https://www.ncbi.nlm.nih.gov/pubmed/37608397 http://dx.doi.org/10.1186/s13104-023-06464-2 |
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