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Multicenter Testing of a Simple Molecular Diagnostic System for the Diagnosis of Mycobacterium Tuberculosis
Mycobacterium tuberculosis (MTB) is a communicable disease and still remains a threat to common health. Thus, early diagnosis and treatment are required to prevent the spread of infection. Despite the recent advances in molecular diagnostic systems, the commonly used MTB diagnostic tools are laborat...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9954000/ https://www.ncbi.nlm.nih.gov/pubmed/36832025 http://dx.doi.org/10.3390/bios13020259 |
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author | Lee, Hyo Joo Kim, Nam Hun Lee, Eun Hye Yoon, Young Soon Jeong, Yun Jeong Lee, Byung Chul Koo, Bonhan Jang, Yoon Ok Kim, Sung-Han Kang, Young Ae Lee, Sei Won Shin, Yong |
author_facet | Lee, Hyo Joo Kim, Nam Hun Lee, Eun Hye Yoon, Young Soon Jeong, Yun Jeong Lee, Byung Chul Koo, Bonhan Jang, Yoon Ok Kim, Sung-Han Kang, Young Ae Lee, Sei Won Shin, Yong |
author_sort | Lee, Hyo Joo |
collection | PubMed |
description | Mycobacterium tuberculosis (MTB) is a communicable disease and still remains a threat to common health. Thus, early diagnosis and treatment are required to prevent the spread of infection. Despite the recent advances in molecular diagnostic systems, the commonly used MTB diagnostic tools are laboratory-based assays, such as mycobacterial culture, MTB PCR, and Xpert MTB/RIF. To address this limitation, point-of-care testing (POCT)-based molecular diagnostic technologies capable of sensitive and accurate detection even in environments with limited sources are needed. In this study, we propose simple tuberculosis (TB) molecular diagnostic assay by combining sample preparation and DNA-detection steps. The sample preparation is performed using a syringe filter with amine-functionalized diatomaceous earth and homobifunctional imidoester. Subsequently, the target DNA is detected by quantitative PCR (polymerase chain reaction). The results can be obtained within 2 h from samples with large volumes, without any additional instruments. The limit of detection of this system is 10 times higher than those of conventional PCR assays. We validated the clinical utility of the proposed method in 88 sputum samples obtained from four hospitals in the Republic of Korea. Overall, the sensitivity of this system was superior to those of other assays. Therefore, the proposed system can be useful for MTB diagnosis in limited-resource settings. |
format | Online Article Text |
id | pubmed-9954000 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-99540002023-02-25 Multicenter Testing of a Simple Molecular Diagnostic System for the Diagnosis of Mycobacterium Tuberculosis Lee, Hyo Joo Kim, Nam Hun Lee, Eun Hye Yoon, Young Soon Jeong, Yun Jeong Lee, Byung Chul Koo, Bonhan Jang, Yoon Ok Kim, Sung-Han Kang, Young Ae Lee, Sei Won Shin, Yong Biosensors (Basel) Article Mycobacterium tuberculosis (MTB) is a communicable disease and still remains a threat to common health. Thus, early diagnosis and treatment are required to prevent the spread of infection. Despite the recent advances in molecular diagnostic systems, the commonly used MTB diagnostic tools are laboratory-based assays, such as mycobacterial culture, MTB PCR, and Xpert MTB/RIF. To address this limitation, point-of-care testing (POCT)-based molecular diagnostic technologies capable of sensitive and accurate detection even in environments with limited sources are needed. In this study, we propose simple tuberculosis (TB) molecular diagnostic assay by combining sample preparation and DNA-detection steps. The sample preparation is performed using a syringe filter with amine-functionalized diatomaceous earth and homobifunctional imidoester. Subsequently, the target DNA is detected by quantitative PCR (polymerase chain reaction). The results can be obtained within 2 h from samples with large volumes, without any additional instruments. The limit of detection of this system is 10 times higher than those of conventional PCR assays. We validated the clinical utility of the proposed method in 88 sputum samples obtained from four hospitals in the Republic of Korea. Overall, the sensitivity of this system was superior to those of other assays. Therefore, the proposed system can be useful for MTB diagnosis in limited-resource settings. MDPI 2023-02-12 /pmc/articles/PMC9954000/ /pubmed/36832025 http://dx.doi.org/10.3390/bios13020259 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Lee, Hyo Joo Kim, Nam Hun Lee, Eun Hye Yoon, Young Soon Jeong, Yun Jeong Lee, Byung Chul Koo, Bonhan Jang, Yoon Ok Kim, Sung-Han Kang, Young Ae Lee, Sei Won Shin, Yong Multicenter Testing of a Simple Molecular Diagnostic System for the Diagnosis of Mycobacterium Tuberculosis |
title | Multicenter Testing of a Simple Molecular Diagnostic System for the Diagnosis of Mycobacterium Tuberculosis |
title_full | Multicenter Testing of a Simple Molecular Diagnostic System for the Diagnosis of Mycobacterium Tuberculosis |
title_fullStr | Multicenter Testing of a Simple Molecular Diagnostic System for the Diagnosis of Mycobacterium Tuberculosis |
title_full_unstemmed | Multicenter Testing of a Simple Molecular Diagnostic System for the Diagnosis of Mycobacterium Tuberculosis |
title_short | Multicenter Testing of a Simple Molecular Diagnostic System for the Diagnosis of Mycobacterium Tuberculosis |
title_sort | multicenter testing of a simple molecular diagnostic system for the diagnosis of mycobacterium tuberculosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9954000/ https://www.ncbi.nlm.nih.gov/pubmed/36832025 http://dx.doi.org/10.3390/bios13020259 |
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