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Visualization of the Charcoal Agar Resazurin Assay for Semi-quantitative, Medium-throughput Enumeration of Mycobacteria

There is an urgent need to discover and progress anti-infectives that shorten the duration of tuberculosis (TB) treatment. Mycobacterium tuberculosis, the etiological agent of TB, is refractory to rapid and lasting chemotherapy due to the presence of bacilli exhibiting phenotypic drug resistance. Th...

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Autores principales: Gold, Ben, Roberts, Julia, Ling, Yan, Lopez Quezada, Landys, Glasheen, Jou, Ballinger, Elaine, Somersan-Karakaya, Selin, Warrier, Thulasi, Nathan, Carl
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MyJove Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5226417/
https://www.ncbi.nlm.nih.gov/pubmed/28060290
http://dx.doi.org/10.3791/54690
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author Gold, Ben
Roberts, Julia
Ling, Yan
Lopez Quezada, Landys
Glasheen, Jou
Ballinger, Elaine
Somersan-Karakaya, Selin
Warrier, Thulasi
Nathan, Carl
author_facet Gold, Ben
Roberts, Julia
Ling, Yan
Lopez Quezada, Landys
Glasheen, Jou
Ballinger, Elaine
Somersan-Karakaya, Selin
Warrier, Thulasi
Nathan, Carl
author_sort Gold, Ben
collection PubMed
description There is an urgent need to discover and progress anti-infectives that shorten the duration of tuberculosis (TB) treatment. Mycobacterium tuberculosis, the etiological agent of TB, is refractory to rapid and lasting chemotherapy due to the presence of bacilli exhibiting phenotypic drug resistance. The charcoal agar resazurin assay (CARA) was developed as a tool to characterize active molecules discovered by high-throughput screening campaigns against replicating and non-replicating M. tuberculosis. Inclusion of activated charcoal in bacteriologic agar medium helps mitigate the impact of compound carry-over, and eliminates the requirement to pre-dilute cells prior to spotting on CARA microplates. After a 7-10 day incubation period at 37 °C, the reduction of resazurin by mycobacterial microcolonies growing on the surface of CARA microplate wells permits semi-quantitative assessment of bacterial numbers via fluorometry. The CARA detects approximately a 2-3 log(10) difference in bacterial numbers and predicts a minimal bactericidal concentration leading to ≥99% bacterial kill (MBC(≥99)). The CARA helps determine whether a molecule is active on bacilli that are replicating, non-replicating, or both. Pilot experiments using the CARA facilitate the identification of which concentration of test agent and time of compound exposure require further evaluation by colony forming unit (CFU) assays. In addition, the CARA can predict if replicating actives are bactericidal or bacteriostatic.
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spelling pubmed-52264172017-01-26 Visualization of the Charcoal Agar Resazurin Assay for Semi-quantitative, Medium-throughput Enumeration of Mycobacteria Gold, Ben Roberts, Julia Ling, Yan Lopez Quezada, Landys Glasheen, Jou Ballinger, Elaine Somersan-Karakaya, Selin Warrier, Thulasi Nathan, Carl J Vis Exp Infection There is an urgent need to discover and progress anti-infectives that shorten the duration of tuberculosis (TB) treatment. Mycobacterium tuberculosis, the etiological agent of TB, is refractory to rapid and lasting chemotherapy due to the presence of bacilli exhibiting phenotypic drug resistance. The charcoal agar resazurin assay (CARA) was developed as a tool to characterize active molecules discovered by high-throughput screening campaigns against replicating and non-replicating M. tuberculosis. Inclusion of activated charcoal in bacteriologic agar medium helps mitigate the impact of compound carry-over, and eliminates the requirement to pre-dilute cells prior to spotting on CARA microplates. After a 7-10 day incubation period at 37 °C, the reduction of resazurin by mycobacterial microcolonies growing on the surface of CARA microplate wells permits semi-quantitative assessment of bacterial numbers via fluorometry. The CARA detects approximately a 2-3 log(10) difference in bacterial numbers and predicts a minimal bactericidal concentration leading to ≥99% bacterial kill (MBC(≥99)). The CARA helps determine whether a molecule is active on bacilli that are replicating, non-replicating, or both. Pilot experiments using the CARA facilitate the identification of which concentration of test agent and time of compound exposure require further evaluation by colony forming unit (CFU) assays. In addition, the CARA can predict if replicating actives are bactericidal or bacteriostatic. MyJove Corporation 2016-12-14 /pmc/articles/PMC5226417/ /pubmed/28060290 http://dx.doi.org/10.3791/54690 Text en Copyright © 2016, Journal of Visualized Experiments http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visithttp://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Infection
Gold, Ben
Roberts, Julia
Ling, Yan
Lopez Quezada, Landys
Glasheen, Jou
Ballinger, Elaine
Somersan-Karakaya, Selin
Warrier, Thulasi
Nathan, Carl
Visualization of the Charcoal Agar Resazurin Assay for Semi-quantitative, Medium-throughput Enumeration of Mycobacteria
title Visualization of the Charcoal Agar Resazurin Assay for Semi-quantitative, Medium-throughput Enumeration of Mycobacteria
title_full Visualization of the Charcoal Agar Resazurin Assay for Semi-quantitative, Medium-throughput Enumeration of Mycobacteria
title_fullStr Visualization of the Charcoal Agar Resazurin Assay for Semi-quantitative, Medium-throughput Enumeration of Mycobacteria
title_full_unstemmed Visualization of the Charcoal Agar Resazurin Assay for Semi-quantitative, Medium-throughput Enumeration of Mycobacteria
title_short Visualization of the Charcoal Agar Resazurin Assay for Semi-quantitative, Medium-throughput Enumeration of Mycobacteria
title_sort visualization of the charcoal agar resazurin assay for semi-quantitative, medium-throughput enumeration of mycobacteria
topic Infection
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5226417/
https://www.ncbi.nlm.nih.gov/pubmed/28060290
http://dx.doi.org/10.3791/54690
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