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A new method for the detection of Mycobacterium tuberculosis based on the CRISPR/Cas system
OBJECT: Mycobacterium tuberculosis (MTB) is a bacterium that can cause zoonoses by aerosol transmission. Tuberculosis (TB) caused by MTB heavily burdens world public health security. Developing efficient, specific, convenient, and inexpensive MTB assays are essential for preventing and controlling T...
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/PMC10568934/ https://www.ncbi.nlm.nih.gov/pubmed/37821806 http://dx.doi.org/10.1186/s12879-023-08656-4 |
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author | Zhang, Xiaoyu He, Xiaoying Zhang, Yubo Chen, Lei Pan, Zhaobao Huang, Yueying Li, Heng |
author_facet | Zhang, Xiaoyu He, Xiaoying Zhang, Yubo Chen, Lei Pan, Zhaobao Huang, Yueying Li, Heng |
author_sort | Zhang, Xiaoyu |
collection | PubMed |
description | OBJECT: Mycobacterium tuberculosis (MTB) is a bacterium that can cause zoonoses by aerosol transmission. Tuberculosis (TB) caused by MTB heavily burdens world public health security. Developing efficient, specific, convenient, and inexpensive MTB assays are essential for preventing and controlling TB. METHODS: In this study, we established a specific detection method for MTB using the Clustered Regularly Interspersed Short Palindromic Repeats (CRISPR) system, combined with recombinase mediated isothermal nucleic acid amplification (RAA) to improve the sensitivity of the detection system and achieve “two-level” amplification of the detection signal. The sensitivity and specificity of RAA combined with the CRISPR/Cas system were analyzed. Using BACTEC 960 culture as the gold standard for detecting MTB, we established the TB-CRISPR technique by testing 504 samples from patients with suspected TB. RESULTS: MTB H37Ra could be seen as low as 3.13 CFU/mL by the CRISPR-Cas12a system targeting IS6110. With BACTEC960 culture (120 positives and 384 negatives) as the gold standard, the sensitivity of the TB-CRISPR technique was 0.883 (0.809–0.932), and the specificity was 0.940 (0.910–0.961). According to the receiver operating characteristic (ROC) curve analysis, the area under the curve (AUC) reached 0.944 (0.914–0.975) within 95% CI. The positive likelihood ratio (PLR) was 14.747 (9.870-22.035), and the negative likelihood ratio (NLR) was 0.124 (0.076–0.203). The positive predictive value (PPV) was 0.822 (0.742–0.881), and the negative predictive value (NPV) was 0.963 (0.937–0.979). CONCLUSION: TB-CRISPR plays an essential role in the molecular diagnosis of TB. The whole detection time is less than 1.5 h. It is easy to operate and does not need complex instruments. It is of great significance for the rapid detection of MTB and the clinical diagnosis of TB. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12879-023-08656-4. |
format | Online Article Text |
id | pubmed-10568934 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-105689342023-10-13 A new method for the detection of Mycobacterium tuberculosis based on the CRISPR/Cas system Zhang, Xiaoyu He, Xiaoying Zhang, Yubo Chen, Lei Pan, Zhaobao Huang, Yueying Li, Heng BMC Infect Dis Research OBJECT: Mycobacterium tuberculosis (MTB) is a bacterium that can cause zoonoses by aerosol transmission. Tuberculosis (TB) caused by MTB heavily burdens world public health security. Developing efficient, specific, convenient, and inexpensive MTB assays are essential for preventing and controlling TB. METHODS: In this study, we established a specific detection method for MTB using the Clustered Regularly Interspersed Short Palindromic Repeats (CRISPR) system, combined with recombinase mediated isothermal nucleic acid amplification (RAA) to improve the sensitivity of the detection system and achieve “two-level” amplification of the detection signal. The sensitivity and specificity of RAA combined with the CRISPR/Cas system were analyzed. Using BACTEC 960 culture as the gold standard for detecting MTB, we established the TB-CRISPR technique by testing 504 samples from patients with suspected TB. RESULTS: MTB H37Ra could be seen as low as 3.13 CFU/mL by the CRISPR-Cas12a system targeting IS6110. With BACTEC960 culture (120 positives and 384 negatives) as the gold standard, the sensitivity of the TB-CRISPR technique was 0.883 (0.809–0.932), and the specificity was 0.940 (0.910–0.961). According to the receiver operating characteristic (ROC) curve analysis, the area under the curve (AUC) reached 0.944 (0.914–0.975) within 95% CI. The positive likelihood ratio (PLR) was 14.747 (9.870-22.035), and the negative likelihood ratio (NLR) was 0.124 (0.076–0.203). The positive predictive value (PPV) was 0.822 (0.742–0.881), and the negative predictive value (NPV) was 0.963 (0.937–0.979). CONCLUSION: TB-CRISPR plays an essential role in the molecular diagnosis of TB. The whole detection time is less than 1.5 h. It is easy to operate and does not need complex instruments. It is of great significance for the rapid detection of MTB and the clinical diagnosis of TB. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12879-023-08656-4. BioMed Central 2023-10-11 /pmc/articles/PMC10568934/ /pubmed/37821806 http://dx.doi.org/10.1186/s12879-023-08656-4 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 Zhang, Xiaoyu He, Xiaoying Zhang, Yubo Chen, Lei Pan, Zhaobao Huang, Yueying Li, Heng A new method for the detection of Mycobacterium tuberculosis based on the CRISPR/Cas system |
title | A new method for the detection of Mycobacterium tuberculosis based on the CRISPR/Cas system |
title_full | A new method for the detection of Mycobacterium tuberculosis based on the CRISPR/Cas system |
title_fullStr | A new method for the detection of Mycobacterium tuberculosis based on the CRISPR/Cas system |
title_full_unstemmed | A new method for the detection of Mycobacterium tuberculosis based on the CRISPR/Cas system |
title_short | A new method for the detection of Mycobacterium tuberculosis based on the CRISPR/Cas system |
title_sort | new method for the detection of mycobacterium tuberculosis based on the crispr/cas system |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10568934/ https://www.ncbi.nlm.nih.gov/pubmed/37821806 http://dx.doi.org/10.1186/s12879-023-08656-4 |
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