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Real-Time Imaging of Mycobacterium tuberculosis Using a Novel Near-Infrared Fluorescent Substrate
Slow growth of Mycobacterium tuberculosis (Mtb), the causative agent of tuberculosis (TB), hinders advancement in all areas of research toward prevention and treatment. Real time imaging, employing reporter enzyme fluorescence (REF) that uses custom fluorogenic substrates for bacterial enzymes, allo...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6061879/ https://www.ncbi.nlm.nih.gov/pubmed/27421748 http://dx.doi.org/10.1093/infdis/jiw298 |
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author | Yang, Hee-Jeong Kong, Ying Cheng, Yunfeng Janagama, Harish Hassounah, Hany Xie, Hexin Rao, Jianghong Cirillo, Jeffrey D. |
author_facet | Yang, Hee-Jeong Kong, Ying Cheng, Yunfeng Janagama, Harish Hassounah, Hany Xie, Hexin Rao, Jianghong Cirillo, Jeffrey D. |
author_sort | Yang, Hee-Jeong |
collection | PubMed |
description | Slow growth of Mycobacterium tuberculosis (Mtb), the causative agent of tuberculosis (TB), hinders advancement in all areas of research toward prevention and treatment. Real time imaging, employing reporter enzyme fluorescence (REF) that uses custom fluorogenic substrates for bacterial enzymes, allows rapid and specific detection of Mtb in live animals. We have synthesized a novel REF substrate, CNIR800, which carries a near-infrared (NIR) fluorochrome IRDye 800CW, with a quencher connected through the lactam ring that is hydrolyzed by the enzyme BlaC (β-lactamase) naturally expressed by Mtb. CNIR800 produces long wavelength emission at 795 nm upon excitation (745 nm) and exhibits significantly improved signal-to-noise ratios for detection of Mtb . The detection threshold with CNIR800 is ∼100 colony forming units (CFU) in vitro and <1000 CFU in the lungs of mice. Additionally, fluorescence signal from cleaved CNIR800 reaches maximal levels at 4-6 h post-administration in live animals, allowing accurate evaluation of anti-tuberculous drug efficacy. Thus, CNIR800 represents an excellent substrate for accurate detection of Mtb rapidly and specifically in animals, facilitating research toward understanding pathogenic mechanisms, evaluation of therapeutic outcomes, and screening new vaccines. |
format | Online Article Text |
id | pubmed-6061879 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-60618792018-08-07 Real-Time Imaging of Mycobacterium tuberculosis Using a Novel Near-Infrared Fluorescent Substrate Yang, Hee-Jeong Kong, Ying Cheng, Yunfeng Janagama, Harish Hassounah, Hany Xie, Hexin Rao, Jianghong Cirillo, Jeffrey D. J Infect Dis Major Article Slow growth of Mycobacterium tuberculosis (Mtb), the causative agent of tuberculosis (TB), hinders advancement in all areas of research toward prevention and treatment. Real time imaging, employing reporter enzyme fluorescence (REF) that uses custom fluorogenic substrates for bacterial enzymes, allows rapid and specific detection of Mtb in live animals. We have synthesized a novel REF substrate, CNIR800, which carries a near-infrared (NIR) fluorochrome IRDye 800CW, with a quencher connected through the lactam ring that is hydrolyzed by the enzyme BlaC (β-lactamase) naturally expressed by Mtb. CNIR800 produces long wavelength emission at 795 nm upon excitation (745 nm) and exhibits significantly improved signal-to-noise ratios for detection of Mtb . The detection threshold with CNIR800 is ∼100 colony forming units (CFU) in vitro and <1000 CFU in the lungs of mice. Additionally, fluorescence signal from cleaved CNIR800 reaches maximal levels at 4-6 h post-administration in live animals, allowing accurate evaluation of anti-tuberculous drug efficacy. Thus, CNIR800 represents an excellent substrate for accurate detection of Mtb rapidly and specifically in animals, facilitating research toward understanding pathogenic mechanisms, evaluation of therapeutic outcomes, and screening new vaccines. Oxford University Press 2016-07 2016-07-15 /pmc/articles/PMC6061879/ /pubmed/27421748 http://dx.doi.org/10.1093/infdis/jiw298 Text en © The Author 2016. Published by Oxford University Press for the Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence ( http://creativecommons.org/licenses/by-nc-nd/4.0/ ), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, contact journals.permissions@oup.com . |
spellingShingle | Major Article Yang, Hee-Jeong Kong, Ying Cheng, Yunfeng Janagama, Harish Hassounah, Hany Xie, Hexin Rao, Jianghong Cirillo, Jeffrey D. Real-Time Imaging of Mycobacterium tuberculosis Using a Novel Near-Infrared Fluorescent Substrate |
title |
Real-Time Imaging of
Mycobacterium tuberculosis
Using a Novel Near-Infrared Fluorescent Substrate
|
title_full |
Real-Time Imaging of
Mycobacterium tuberculosis
Using a Novel Near-Infrared Fluorescent Substrate
|
title_fullStr |
Real-Time Imaging of
Mycobacterium tuberculosis
Using a Novel Near-Infrared Fluorescent Substrate
|
title_full_unstemmed |
Real-Time Imaging of
Mycobacterium tuberculosis
Using a Novel Near-Infrared Fluorescent Substrate
|
title_short |
Real-Time Imaging of
Mycobacterium tuberculosis
Using a Novel Near-Infrared Fluorescent Substrate
|
title_sort | real-time imaging of
mycobacterium tuberculosis
using a novel near-infrared fluorescent substrate |
topic | Major Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6061879/ https://www.ncbi.nlm.nih.gov/pubmed/27421748 http://dx.doi.org/10.1093/infdis/jiw298 |
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