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Chemiluminescent Protease Probe for Rapid, Sensitive, and Inexpensive Detection of Live Mycobacterium tuberculosis
[Image: see text] Tuberculosis (TB) is a top-ten cause of death worldwide. Successful treatment is often limited by insufficient diagnostic capabilities, especially at the point of care in low-resource settings. The ideal diagnostic must be fast, be cheap, and require minimal clinical resources whil...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8161474/ https://www.ncbi.nlm.nih.gov/pubmed/34079897 http://dx.doi.org/10.1021/acscentsci.0c01345 |
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author | Babin, Brett M. Fernandez-Cuervo, Gabriela Sheng, Jessica Green, Ori Ordonez, Alvaro A. Turner, Mitchell L. Keller, Laura J. Jain, Sanjay K. Shabat, Doron Bogyo, Matthew |
author_facet | Babin, Brett M. Fernandez-Cuervo, Gabriela Sheng, Jessica Green, Ori Ordonez, Alvaro A. Turner, Mitchell L. Keller, Laura J. Jain, Sanjay K. Shabat, Doron Bogyo, Matthew |
author_sort | Babin, Brett M. |
collection | PubMed |
description | [Image: see text] Tuberculosis (TB) is a top-ten cause of death worldwide. Successful treatment is often limited by insufficient diagnostic capabilities, especially at the point of care in low-resource settings. The ideal diagnostic must be fast, be cheap, and require minimal clinical resources while providing high sensitivity, selectivity, and the ability to differentiate live from dead bacteria. We describe here the development of a fast, luminescent, and affordable sensor of Hip1 (FLASH) for detecting and monitoring drug susceptibility of Mycobacterium tuberculosis (Mtb). FLASH is a selective chemiluminescent substrate for the Mtb protease Hip1 that, when processed, produces visible light that can be measured with a high signal-to-noise ratio using inexpensive sensors. FLASH is sensitive to fmol of recombinant Hip1 enzyme in vitro and can detect as few as thousands of Mtb cells in culture or in human sputum samples within minutes. The probe is highly selective for Mtb compared to other nontuberculous mycobacteria and can distinguish live from dead cells. Importantly, FLASH can be used to measure antibiotic killing of Mtb in culture with greatly accelerated timelines compared to traditional protocols. Overall, FLASH has the potential to enhance both TB diagnostics and drug resistance monitoring in resource-limited settings. |
format | Online Article Text |
id | pubmed-8161474 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-81614742021-06-01 Chemiluminescent Protease Probe for Rapid, Sensitive, and Inexpensive Detection of Live Mycobacterium tuberculosis Babin, Brett M. Fernandez-Cuervo, Gabriela Sheng, Jessica Green, Ori Ordonez, Alvaro A. Turner, Mitchell L. Keller, Laura J. Jain, Sanjay K. Shabat, Doron Bogyo, Matthew ACS Cent Sci [Image: see text] Tuberculosis (TB) is a top-ten cause of death worldwide. Successful treatment is often limited by insufficient diagnostic capabilities, especially at the point of care in low-resource settings. The ideal diagnostic must be fast, be cheap, and require minimal clinical resources while providing high sensitivity, selectivity, and the ability to differentiate live from dead bacteria. We describe here the development of a fast, luminescent, and affordable sensor of Hip1 (FLASH) for detecting and monitoring drug susceptibility of Mycobacterium tuberculosis (Mtb). FLASH is a selective chemiluminescent substrate for the Mtb protease Hip1 that, when processed, produces visible light that can be measured with a high signal-to-noise ratio using inexpensive sensors. FLASH is sensitive to fmol of recombinant Hip1 enzyme in vitro and can detect as few as thousands of Mtb cells in culture or in human sputum samples within minutes. The probe is highly selective for Mtb compared to other nontuberculous mycobacteria and can distinguish live from dead cells. Importantly, FLASH can be used to measure antibiotic killing of Mtb in culture with greatly accelerated timelines compared to traditional protocols. Overall, FLASH has the potential to enhance both TB diagnostics and drug resistance monitoring in resource-limited settings. American Chemical Society 2021-04-14 2021-05-26 /pmc/articles/PMC8161474/ /pubmed/34079897 http://dx.doi.org/10.1021/acscentsci.0c01345 Text en © 2021 The Authors. Published by American Chemical Society Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Babin, Brett M. Fernandez-Cuervo, Gabriela Sheng, Jessica Green, Ori Ordonez, Alvaro A. Turner, Mitchell L. Keller, Laura J. Jain, Sanjay K. Shabat, Doron Bogyo, Matthew Chemiluminescent Protease Probe for Rapid, Sensitive, and Inexpensive Detection of Live Mycobacterium tuberculosis |
title | Chemiluminescent Protease Probe for Rapid, Sensitive,
and Inexpensive Detection of Live Mycobacterium tuberculosis |
title_full | Chemiluminescent Protease Probe for Rapid, Sensitive,
and Inexpensive Detection of Live Mycobacterium tuberculosis |
title_fullStr | Chemiluminescent Protease Probe for Rapid, Sensitive,
and Inexpensive Detection of Live Mycobacterium tuberculosis |
title_full_unstemmed | Chemiluminescent Protease Probe for Rapid, Sensitive,
and Inexpensive Detection of Live Mycobacterium tuberculosis |
title_short | Chemiluminescent Protease Probe for Rapid, Sensitive,
and Inexpensive Detection of Live Mycobacterium tuberculosis |
title_sort | chemiluminescent protease probe for rapid, sensitive,
and inexpensive detection of live mycobacterium tuberculosis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8161474/ https://www.ncbi.nlm.nih.gov/pubmed/34079897 http://dx.doi.org/10.1021/acscentsci.0c01345 |
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