We are grateful to Kristin Burns-Huang for expert review of the manuscript and J. David Warren (Weill Cornell Medical College) for chemistry assistance while developing the CARA. This work was supported by the TB Drug Accelerator Program of the Bill and Melinda Gates Foundation, the Abby and Howard P. Milstein Program in Translational Medicine, and an NIH TB Research Unit (U19 AI111143). The Department of Microbiology and Immunology is supported by the William Randolph Hearst Foundation. SSK was supported by NIH grant K08AI108799.

1. Preparation of CARA Microplates
<ol>
	<li>Autoclave 900 ml of Middlebrook 7H11 agar containing 0.2% glycerol and 0.4% activated charcoal in a 2 L Erlenmeyer flask, or alternatively, 450 ml in a 1 L glass beaker. Include a large autoclavable stir bar in the flask or beaker. Cover the opening of the flask or beaker with aluminum foil and attach to glass with autoclave tape.</li>
	<li>Cool to touch (approximately 55-65 &#176;C) on a magnetic stir plate set at a low speed to maintain the charcoal in suspension.</li>
	<li>Perform all subsequent steps aseptically in a biosafety hood that has a magnetic stir plate.</li>
	<li>Remove foil. Add 100 ml OADC supplement (OADC supplement, when used at 10%, yields final media concentrations of 0.2% dextrose, 0.5% albumin, 0.085% NaCl, 0.0005% oleic acid, and 0.4 mg/ml catalase) to the 2 L Erlenmeyer flask, or 50 ml OADC to the 1 L beaker, and continue mixing.</li>
	<li>If using an Erlenmeyer flask, pour approximately 25-40 ml of 7H11-OADC-charcoal into a sterile reagent reservoir. If using the beaker, it is not necessary to use a reagent reservoir.</li>
	<li>Fill a 96-well microplate with 200 &#956;l/well of 7H11-OADC-charcoal from the reagent reservoir or beaker. Work quickly to avoid agar solidification and introduction of bubbles. Avoid splashing solid medium outside of the wells, as that can be a source of fungal contamination. Using a multichannel pipette, use one set of 12 filter tips for the transfer of 7H11-OADC-charcoal to the 8 rows (A-H) of the 96-well plate. 
	NOTE: The medium solidifies quickly. To avoid clogging pipette tips, change them frequently.</li>
	<li>Alternatively, pour CARA microplates using a p1000 electronic multichannel pipette with filter tips to assist in preparing numerous plates. 
	NOTE: Due to the low volume of microplate wells, the agar in CARA microplates solidifies within minutes of pouring.</li>
	<li>Place stacks of CARA microplates in resealable plastic bags to avoid drying out.</li>
	<li>Store CARA microplates at 4 &#176;C.</li>
</ol>
2. Setting Up Replicating and Non-replicating MIC90 Assays
<ol>
	<li>Inoculate M. tuberculosis, M. bovis BCG or M. smegmatis at an OD580 of 0.01-0.1 and expand to mid-log phase (OD580 ~0.5) in Middlebrook 7H9-ADN (Middlebrook 7H9 containing 0.2% glycerol, 0.2% dextrose, 0.5% albumin, and 0.085% NaCl) or 7H9-OADC (Middlebrook 7H9 containing 0.2% glycerol and 10% OADC supplement).</li>
	<li>Grow M. tuberculosis and M. bovis BCG as ~20 ml standing cultures in cell culture flasks and M. smegmatis with shaking in polypropylene round-bottom (4 ml culture) or 50 ml conical centrifuge tubes (10-20 ml culture). Incubate pathogenic mycobacteria at 37 &#176;C with 20% O2 and 5% CO2, and M. smegmatis at 37 &#176;C with 20% O2.</li>
	<li>Set up a minimal-inhibitory concentration (MIC90)-style experiment under replicating and non-replicating conditions (Figure 2). 
	NOTE: Test agents are usually assayed in duplicates or quadruplicates to permit testing 4, or 2 compounds, respectively, per 96-well microplate. For example, in a 96-well plate, one test agent can be assayed in rows A-D and another in rows E-H. The DMSO (vehicle) is in columns 1, 2, and 12, and the test agent dilution series runs from column 3 (lowest concentration) to column 11 (highest concentration). MIC90-style assays typically employ 2-fold dilution series. There are numerous non-replicating models available for mycobacteria14-16,18,24,25 and for illustrative purposes, we are using a multi-stress model of non-replication6,8,9.
	<ol>
		<li>For the replicating assay, distribute 200 &#956;l cells in 7H9-ADN at an OD580 of 0.01 into all wells of a clear-bottomed, tissue culture treated 96-well plate.</li>
		<li>For the non-replicating assay, wash cells twice in phosphate buffered saline (PBS) containing 0.02% tyloxapol, and resuspend cells in non-replicating medium (0.05% KH2PO4, 0.05% MgSO4, 0.005% ferric ammonium citrate, 0.0001% ZnCl2, 0.1% NH4Cl, 0.5% BSA, 0.085% NaCl, 0.02% tyloxapol, 0.05% butyrate; pH adjusted to 5.0 with 2 N NaOH).
		<ol>
			<li>Dilute cells to an OD580 of 0.1 in non-replicating medium and add NaNO2 from a freshly prepared 1 M stock to a final concentration of 0.5 mM.</li>
			<li>Distribute 200 &#956;l cells at an OD580 of 0.1 into all wells of a clear-bottomed, tissue culture treated 96-well plate. 
			NOTE: Prepare compound dilutions as 100-fold stock solutions in DMSO. Thus, a typical MIC plate testing the impact of a molecule at a final concentration 0.4-100 &#956;g/ml would require stock solutions of 0.04-10 mg/ml in DMSO.</li>
		</ol>
		</li>
		<li>Add 2 &#956;l of dilutions of test agent 1 into rows A-E and 2 &#956;l of dilutions of test agent 2 into rows E-H. Mix thoroughly.</li>
		<li>Add 2 &#956;l vehicle control (usually DMSO) into control wells, columns 1, 2, 12 (rows A-H). Mix thoroughly.</li>
		<li>For each experiment, include at least one positive control such as rifampicin from 0.004 to 1 &#956;g/ml (replicating assay) and/or 0.08 to 20 &#956;g/ml (non-replicating assay). 
		NOTE: The use of 6-bromo-1H-indazol-3-amine9 at 0.1 to 25 &#956;g/ml is recommended as a control compound that has selective, NaNO2-dependent activity in the multi-stress model of non-replication.</li>
		<li>For replicating assays, incubate microplates at 37 &#176;C at 20% O2 and 5% CO2 for 7 days (M. tuberculosis and M. bovis BCG) or 1-48 hr (M. smegmatis). For the multi-stress model of non-replication, incubate microplates for 7 days at 37 &#176;C at 1% O2 and 5% CO2 (M. tuberculosis and M. bovis BCG).</li>
	</ol>
	</li>
</ol>
3. Inoculation of CARA Microplates
<ol>
	<li>At time points in which the CARA will be used as a read-out, carefully resuspend well contents of the MIC90-style assay plate using a p200 multichannel pipette set at 50-75 &#956;l. Pipette up and down at least 5-10 times and gently swirl the well contents in a circular motion using the pipette tips.</li>
	<li>Transfer 10 &#956;l of assay well contents to the CARA microplate. Ensure that the order of the well contents on the assay plate matches the order of the well contents of the CARA microplate. Avoid splashing during the transfers and make sure the 10 &#956;l are spotted into the middle of the CARA microplate wells. Confirm the 10 &#956;l absorbs into the CARA microplate. 
	NOTE: There are no dilutions required prior to spotting cells on the CARA microplates.</li>
	<li>Bind stacks of CARA microplates with plate tape and then place into a resealable plastic bag. Incubate CARA microplates at 37 &#176;C with 20% O2 (M. smegmatis) or 1% O2 and 5% CO2 (M. tuberculosis and M. bovis BCG).</li>
	<li>For M. tuberculosis and M. bovis BCG, replicating assays: incubate for 7 days; for M. tuberculosis and M. bovis BCG non-replicating assays, incubate for 10 days; for M. smegmatis, replicating assays, incubate for 1-2 days; for M. smegmatis, non-replicating assays, incubate 2-3 days. 
	NOTE: Times are estimates and may be modified accordingly for different replicating, non-replicating, and stress conditions.</li>
</ol>
4. Developing CARA Microplates
<ol>
	<li>Develop the CARA microplates when a film of bacterial growth, or larger, macroscopic colonies, are visible on the negative (vehicle) control wells. 
	NOTE: After prolonged incubation, CARA microplate wells often appear dry and we recommend pre-wetting well contents with sterile PBS. This serves to prevent the charcoal from absorbing resazurin, which can lead to low fluorescence or well-to-well variation.</li>
	<li>Using a single set of 12 p200 tips with a multichannel pipette, dispense 40 &#181;l of sterile PBS along the side of the wells and allow the PBS to distribute across the top of the agar/bacterial microcolonies.</li>
	<li>Prepare CARA developing reagent by mixing 5 mg resazurin (0.01% final) and 50 ml of 5% Tween80 in PBS. Vortex and sterile filter. 
	NOTE: An alternative CARA developing reagent can be prepared by mixing commercially prepared resazurin liquid solution at 1:1 (vol/vol) with 10% Tween80 in PBS.</li>
	<li>Add 50 &#181;l of freshly prepared CARA developing reagent to each well of the CARA microplate using a 12-channel pipette. Rock plates back and forth a few times to help distribute reagent across the agar and bacterial mat in each well.</li>
	<li>Place the plates in a resealable plastic bag and incubate at 37 &#176;C for at least 30 min for M. smegmatis and 45-60 min for M. tuberculosis or M. bovis BCG. 
	NOTE: If the vehicle control wells fail to turn pink within the first hour, the plates can be re-bagged and incubated for longer periods of time.</li>
	<li>Prior to reading fluorescence, place CARA microplates in a biosafety hood for 15 min at room temperature with their lids removed. When using BSL3 spectrophotometers outside of a biosafety cabinet, adhere an optical quality PCR sticker over the plate and seal tightly by pressing gently on the sticker surface with a soft paper towel.</li>
	<li>Determine fluorescence via top read with excitation at 530 nm and emission at 590 nm. It is not necessary to blank the plate.</li>
</ol>
5. Data Analysis
<ol>
	<li>Plot inhibitor concentration on the X-axis on a log10 scale and fluorescence on the Y-axis on a linear scale. Use a scatter plot employing a curve fit such as &#34;log inhibitor versus response-variable slope (4 parameters)&#34;. Plot data points as means &#177; standard error.</li>
</ol>

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There are no conflicts of interest to disclose.

The CARA was originally developed to alleviate a bottleneck in progressing non-replicating or dual-active molecules7. The CARA serves as an intermediate step between concentration-response confirmation of primary screening hits and CFU assays (Figure 1). Since a single CARA plate can replace numerous microtiter plates required to prepare serial dilutions, and agar-containing Petri plates used to enumerate surviving bacteria, the CARA provides a simple means to rapidly assess a molecule&#39;s activity and test multiple variables at once, including compound concentration and time of exposure to the compound.
In a CFU assay, in addition to serial dilutions that often range up to 106-fold, the agar plate typically dilutes molecules by an additional ~800-fold (10 &#956;l onto 8 ml in a tri-style Petri plate). Our two-stage, multi-stress screening assay for compounds active on non-replicating M. tuberculosis has a carry-over factor of 5-fold, that is, a compound present in the non-replicating stage of the assay is present at one-fifth the original concentration in the outgrowth (replicating) phase of the assay6-9. The CARA mitigates carry-over effects by sequestering small molecules with activated charcoal. The majority of tuberculosis drugs and clinical candidates bind activated charcoal rapidly and completely, with the exception of the aminoglycoside streptomycin7. Inclusion of activated charcoal in agar plates for CFU assays prevented bacterial growth inhibition, or bacterial kill, by carried-over TMC207 and PA-8247,21,22. Thus, by virtue of incorporating activated charcoal in the bacteriologic agar, the CARA is not dependent on serial dilutions of cells and test agent.
The CARA can help predict bacteriostatic or bactericidal impact of replicating actives and bactericidal impact of non-replicating actives. In general, the CARA is used in parallel with standard MIC90 assays. The predictive power of the CARA comes from comparing MIC90 and CARA results (Figure 2 and Table 1). When used to study anti-mycobacterial agents, the CARA can accurately predict activity that is replicating bactericidal (Figure 4a), replicating bacteriostatic (Figure 4b), non-replicating bactericidal (Figure 4c), or dual active (Figure 4d). The CARA also permits simple evaluation of a compound&#39;s activity across both dose and time. CFU assays alone require a lot of effort and material to assess activity of a compound over a wide range of doses and times, but the task becomes manageable when CARA results narrow the range of conditions to those in which the compound is demonstrably active (Figure 5).
While the CARA has utility in studying the action of anti-infectives on mycobacteria, the assay has limitations. The CARA has a narrow dynamic range (2-3 log10) and may not be appropriate for conditions in which one anticipates there may not be more than 2 to 3 log10 bacterial kill. CARA predictions require further study using a more stringent and accurate method to enumerate bacterial numbers, such as a CFU assay. The post-antibiotic effect of some anti-infectives, such as PAS, can confound the CARA as a predictive tool to distinguish between compounds with bactericidal and bacteriostatic activity against replicating M. tuberculosis7.
There are two recommendations to improve the quality of the CARA. First, one must pour CARA microplates rapidly before the agar solidifies, while maintaining volumetric accuracy and avoiding splashing outside of microwells. Regardless of the number of plates required, we recommend making 0.5 to 1 L batches of medium to help maintain the medium in liquid form for the duration of the time required to pour plates. Changing tips frequently while filling microplates with medium avoids using partially clogged tips. Second, one must minimize artifactual variability in fluorescence between replicates. Mycobacterial microcolonies, in particular for pathogenic mycobacteria such as M. tuberculosis, often grow erratically. For example, microcolonies growing on the agar surface may vary in size, shape, height, or may extend up to the interior walls of microplate wells. One challenge is to cover all bacilli uniformly with the developing reagent. Another hurdle is that after prolonged incubation at 37 &#176;C, the solid bacteriologic medium of the CARA microplates may become dry and prone to absorbing the developing reagent. Since activated charcoal can bind resazurin and quench fluorescence7, there may be well-to-well variation due to dry wells absorbing the resazurin developing solution and the activated charcoal quenching resazurin fluorescence. Pre-wetting the surface of all CARA microplate wells with PBS immediately before adding the developing reagent mitigates both of these problems &#8212; the developing reagent will reach all mycobacterial colonies equally, and the resazurin remains safely above the activated charcoal. The CARA may have applications in identifying and characterizing phenotypes of mycobacterial mutants, or in medium-throughput drug discovery assays for other bacterial species.

Mycobacterium tuberculosis, the etiological agent of tuberculosis, can survive in a host in a latent state that is refractory to antibiotic eradication. Phenotypic (non-genetic) resistance of M. tuberculosis during infection is believed to be due, in part, to populations of non-replicating bacilli1,2. Class I persisters displaying phenotypic drug resistance arise via rare stochastic mechanisms amongst large populations of drug sensitive cells3,4. Class II persisters are rendered non-replicating by factors of host immunity, including external stresses in microenvironments encountered during infection. We recently developed an in vitro model of Class II non-replicating persistence to mimic conditions confronted by M. tuberculosis in activated macrophages and granulomas. The multi-stress model of Class II persistence includes conditions that slow growth, such as a fatty acid carbon source, and completely halt growth, such as mild acidity (pH 5.0), hypoxia (1% O2), and nitric oxide and other reactive nitrogen intermediates5-9. Large-scale screening employing this multi-stress model of non-replication, and other Class II non-replicating models, has yielded diverse molecules whose activity is directed against the non-replicating state5-7,9-18. The same non-replicating screens also revealed a category of molecules that possess activity against both replicating and non-replicating bacilli, termed &#34;dual actives&#34;7,10,12,19,20.
Antibacterial drug discovery in the hit-to-lead phase entails extensive characterization of candidate molecules to choose leads for hit expansion, preliminary pharmacologic characterization, target identification, and preliminary in vivo efficacy studies. As an early step, anti-infectives are classified by their bacteriostatic or bactericidal mechanism of action and, if bactericidal, whether bacterial kill is time- and/or concentration-dependent. The colony forming unit (CFU) assay is the classical, gold standard method to address these questions. In the CFU assay, bacteria are exposed to a test agent, after which aliquots are removed, serially diluted, and aliquots of dilutions are spread on solid bacteriologic medium and incubated to permit growth of surviving cells. Finally, bacterial colonies are enumerated. The CFU assay requires large numbers of microtiter plates to dilute cells and agar-containing Petri-plates to enumerate surviving colonies. The CFU assay for slow growing mycobacteria is hampered by their slow generation time (18-24 hr), which requires approximately 3 weeks for colonies to appear on plates. Furthermore, incubator space is often limited in specialized biosafety-level-3 facilities.
While cumbersome, CFU assays are the gold standard to characterize the impact of non-replicating and dual-active molecules on mycobacteria. Non-replicating assays are subject to high false-positive rates as many are coupled to replicating assays to assess cellular viability6-8. For example, a compound that has potent activity against replicating M. tuberculosis (a &#34;replicating active&#34;) may fail to kill during the non-replicating assay, yet can still kill by virtue of carry-over from the non-replicating phase of the assay to the recovery phase of the assay, which is conducted under conditions that support replication (&#34;replicating conditions&#34;). Compound carry over further complicates analysis of dual active molecules, making it difficult to distinguish whether activity was replicating, non-replicating, or dual.
To address the issues described above, we developed the charcoal agar resazurin assay (CARA) for rapid, semi-quantitative enumeration of mycobacterial species such as M. tuberculosis, M. bovis BCG, and M. smegmatis7 (Figures 1 and 2). In buffer solutions in vitro, activated charcoal rapidly sequesters most of the standard drugs used to treat tuberculosis7. Activated charcoal in CARA microplates binds compounds that may carry over from an assay microplate, and this feature of the CARA eliminates the requirement to serially dilute assay well contents prior to enumeration7,21,22. The number of mycobacterial microcolonies on the agar surface of CARA microplates is estimated by the addition of resazurin, a blue dye, whose reduced form, resorufin, is a pink molecule whose fluorescence is measured by a spectrophotometry23. CARA microplates are incubated for 1-2 days for M. smegmatis and 7-10 days for slow growing mycobacteria such as M. tuberculosis and M. bovis BCG. The CARA has a narrow dynamic range of ~2-3 log10 difference in CFU. When used instead of a CFU assay, a single CARA microplate replaces approximately five 96-well plates used for serial dilutions and 120 tri-style agar plates used for plating. Interpretation of CARA data helps guide subsequent studies by determining which incubation times and compound concentrations to test in more laborious CFU-based assays.

<table><tbody><tr><td>Middlebrook 7H9</td><td>Beckton Dickinson</td><td>271310</td><td></td></tr><tr><td>Middlebrook 7H11</td><td>Beckton Dickinson</td><td>298810</td><td></td></tr><tr><td>Middlebrook OADC</td><td>Beckton Dickinson</td><td>212351</td><td></td></tr><tr><td>BSA, heat shock</td><td>Roche</td><td>3118958001</td><td></td></tr><tr><td>activated charcoal</td><td>Sigma</td><td>C5510</td><td></td></tr><tr><td>PBS, Dulbecco&#039;s Ca&lt;sup&gt;2+&lt;/sup&gt; and Mg&lt;sup&gt;2+&lt;/sup&gt; free</td><td>Life Technologies / Invitrogen</td><td>14190-144</td><td></td></tr><tr><td>tween 80</td><td>Sigma</td><td>P8074</td><td></td></tr><tr><td>tyloxapol</td><td>Sigma</td><td>T8761</td><td></td></tr><tr><td>sodium nitrite</td><td>Sigma</td><td>2252</td><td></td></tr><tr><td>rifampicin</td><td>Sigma</td><td>R3501</td><td></td></tr><tr><td>6-bromo-1H-indazol-3-amine</td><td>Alfa Aesar</td><td>H34095</td><td></td></tr><tr><td>potassium phosphate monobasic&amp;nbsp;&amp;nbsp;</td><td>Sigma</td><td>P0662</td><td></td></tr><tr><td>magnesium sulfate, heptahydrate&amp;nbsp;</td><td>Sigma</td><td>M1880</td><td></td></tr><tr><td>ferric ammonium citrate&amp;nbsp;</td><td>Sigma</td><td>F5879</td><td></td></tr><tr><td>zinc sulfate, heptahydrate</td><td>Sigma</td><td>Z0251</td><td></td></tr><tr><td>ammonium chloride&amp;nbsp;</td><td>Sigma</td><td>A9434</td><td></td></tr><tr><td>butyric acid, liquid</td><td>Sigma</td><td>B103500</td><td></td></tr><tr><td>resazurin powder</td><td>Sigma</td><td>R7017</td><td></td></tr><tr><td>sodium chloride&amp;nbsp;</td><td>J.T. Baker</td><td>4058-01&amp;nbsp;</td><td></td></tr><tr><td>prepared resazurin solution&amp;nbsp;</td><td>Invitrogen</td><td>DAL1100</td><td></td></tr><tr><td>PCR stickers</td><td>Denville</td><td>B1212-5</td><td></td></tr><tr><td>spectrophotometer</td><td>Molecular Devices</td><td>M5</td><td></td></tr><tr><td>96-well, tissue culture treated microplates</td><td>Corning</td><td>3595</td><td></td></tr><tr><td>reagent reservoirs</td><td>VWR&amp;nbsp;</td><td>89094-678</td><td></td></tr><tr><td>resealable plastic bags</td><td>VWR&amp;nbsp;</td><td>395-94602</td><td></td></tr><tr><td>14 ml Polypropylene round-bottom tubes</td><td>Corning&amp;nbsp;</td><td>352059</td><td></td></tr><tr><td>50 ml conical centrifuge tube</td><td>Corning</td><td>352070</td><td></td></tr><tr><td>75 cm&lt;sup&gt;2&lt;/sup&gt; Cell culture flask</td><td>Corning</td><td>431464U</td><td></td></tr><tr><td>clear, flat bottom tissue culture treated 96-well microplate</td><td>Costar</td><td>3595</td><td></td></tr><tr><td>Prism 6 for OS X</td><td>GraphPad</td><td>http://www.graphpad.com/scientific-software/prism/</td><td></td></tr></tbody></table>

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. 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 &#176;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 log10 difference in bacterial numbers and predicts a minimal bactericidal concentration leading to &#8805;99% bacterial kill (MBC&#8805;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.

Anticipated CARA results are described in Figure 2 and summarized in Table 1. For replicating cells, the CARA is run in parallel with a standard MIC90 assays, and for non-replicating assays, the CARA is run in parallel with an adapted MIC90 assay that is coupled to an outgrowth phase. The concentration of test agent that results in failure of CARA-fluorescence to rise above background levels is the CARA-MBC&#8805;99 (Figure 3a). The &#34;&#8805;99&#34; subscript indicates that the CARA-MBC provides an estimated concentration of test agent that gives rise to &#8805;2 log10 bacterial kill (&#8805;99% kill).
The liquid broth MIC90 assay is unable to discriminate between bactericidal and bacteriostatic activity and this distinction has to be resolved by a CFU assay. By convention, the threshold that distinguishes bactericidal from bacteriostatic activity for slow-growing mycobacteria is approximately 2-3 log10 kill over 7 days7,26. Since the dynamic range of the CARA is also 2-3 log10 kill, the CARA can provide an estimate of bactericidal or bacteriostatic activity. The CARA easily identifies some replicating actives as bacteriostatic due to failure of these compounds to decrease CARA fluorescence to background levels (Figure 2). However, some compounds with bacteriostatic activity against replicating M. tuberculosis have a potent post-antibiotic effect, meaning that they continue to inhibit regrowth of bacteria during the recovery phase even in the absence of compound carry-over. This effect can be difficult to recognize in the CARA assay. Compounds are suspected of exerting a post-antibiotic effect if they display a &#34;static window&#34;, defined as a &#62;4-fold shift to the right between the MIC and CARA curves (Figure 3b). The static window indicates that a molecule active against replicating M. tuberculosis may be bacteriostatic instead of bactericidal. In some cases, the static windows are apparent only after inspection of an expanded Y-axis for CARA fluorescence (Figure 3c and 3d).
CARA and MIC90 data are usually plotted together (Figure 4). Representative data for replicating- and non-replicating-active molecules tested by MIC90 and CARA are shown in Figure 4. There are 4 major activity classes for molecules: 1) replicating bactericidal (demonstrated with isoniazid, Figure 4a); 2) replicating bacteriostatic (demonstrated with linezolid, Figure 4b); 3) non-replicating bactericidal (demonstrated with oxyphenbutazone, Figure 4c); and, 4) replicating-active (bacteriostatic or bactericidal) and non-replicating bactericidal (demonstrated with PA-824, Figure 4d). Importantly, Figures 4a and 4b demonstrate that while isoniazid and linezolid appear to have activity against non-replicating bacteria by the MIC90 assay, the CARA suggests they are inactive under the non-replicating conditions tested. To test the utility of the CARA in predicting a molecule&#39;s time- and concentration-dependent impact, replicating M. smegmatis was exposed to increasing concentrations of rifampicin (Figures 5a-d), and at various times between 1-24 hr, aliquots were spotted onto CARA plates. These data indicated that rifampicin exerted an impact as early as 1 hr (Figure 5a), displayed increasing bactericidal activity between 3 and 24 hr (Figures 5b-d), and killed &#8805;2-3 log10 at ~10 &#956;g/ml by 24 hr (Figure 5d). A similar experiment testing quadruplicates of a vehicle control and 9 drug concentrations, and at 4 time points, would be prohibitive by a standard CFU-based assay.
Thus, the CARA has a role in drug discovery as a medium-throughput, rapid mechanism to identify a molecule&#39;s activity profile. CARA predictions should be rigorously evaluated using a standard CFU assay. The addition of 0.4% activated charcoal to Petri plates for CFU analysis may help improve correlation to CARA data, and may result in more accurate CFU counts, the magnitude of the correction generally being proportional to the compound&#39;s potency21,22.
<img alt="Figure 1" src="/files/ftp_upload/54690/54690fig1.jpg" /> 
Figure 1: The CARA is a predictive tool in drug discovery. This diagram summarizes the utility of the CARA as an intermediate stage between drug screening (single point screening, cherry-picking, and dose-response assays) and time-consuming hit-to-lead assays (CFU assays and target identification). [Adapted with permission from Gold et al., Antimicrobial Agents and Chemotherapy, 2015 7] <a href="https://cloudflare-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/54690/54690fig1large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 2" src="/files/ftp_upload/54690/54690fig2.jpg" /> 
Figure 2: Schematic of the broth MIC90 assay and CARA with anticipated results. Both MIC90 and CARA results are presented for 8 possible activities. The color-coding for MIC90 microplate wells is white (no growth) and brown (growth), and for CARA microplates is black (no fluorescence) and pink (resorufin fluorescence). Data are hypothetical. [Adapted with permission from Gold et al., Antimicrobial Agents and Chemotherapy, 2015 7] <a href="https://cloudflare-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/54690/54690fig2large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 3" src="/files/ftp_upload/54690/54690fig3.jpg" /> 
Figure 3: Specialized CARA terms and definitions. The minimal bactericidal concentration of a molecule resulting in background levels of CARA fluorescence is the CARA-MBC&#8805;99 (a). Under replicating conditions, a &#8805;4-fold shift of the CARA-MBC&#8805;99 to the right of the MIC90 often indicates bacteriostatic activity and is called a &#34;static window&#34; (b). For molecules with a potent post-antibiotic effect, static windows may be difficult to observe (c) and require expansion of the Y-axis (CARA fluorescence) to visualize (d). Data are hypothetical. [Adapted with permission from Gold et al., Antimicrobial Agents and Chemotherapy, 2015 7] <a href="https://cloudflare-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/54690/54690fig3large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 4" src="/files/ftp_upload/54690/54690fig4.jpg" /> 
Figure 4: Illustrative MIC90 and CARA results for select compounds. Data for MIC90 (red) and CARA (blue) are demonstrated for (a) isoniazid (INH), (b) linezolid, (c) oxyphenbutazone, and (d) PA-824. Wild-type M. tuberculosis H37Rv was exposed to compounds for 7 days under standard replicating conditions or the multi-stress model of non-replication7-9. MIC90 assays and CARA were performed as shown in Figure 2. [Adapted with permission from Gold et al., Antimicrobial Agents and Chemotherapy, 2015 7] <a href="https://cloudflare-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/54690/54690fig4large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 5" src="/files/ftp_upload/54690/54690fig5.jpg" /> 
Figure 5: Dose- and time-dependent activity of rifampicin. The non-pathogenic, fast-growing M. smegmatis was exposed to increasing concentrations of rifampicin under replicating conditions and aliquots were sampled for CARA at 1 (a), 3 (b), 6 (c) and 24 (d) hr. [Adapted with permission from Gold et al., Antimicrobial Agents and Chemotherapy, 2015 7] <a href="https://cloudflare-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/54690/54690fig5large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Table 1" src="/files/ftp_upload/54690/54690tbl1.jpg" /> 
Table 1: Summary of anticipated results in Figure 2. [Adapted with permission from Gold et al., Antimicrobial Agents and Chemotherapy, 2015 7] <a href="https://cloudflare-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/54690/54690tbl1large.jpg" target="_blank">Please click here to view a larger version of this table.</a>

Watch this Scientific Journal Video about Visualization of the Charcoal Agar Resazurin Assay for Semi-quantitative, Medium-throughput Enumeration of Mycobacteria at JoVE.com

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

The charcoal agar resazurin assay (CARA) is a semi-quantitative, medium-throughput method to assess activity of test agents against mycobacteria that are replicating, non-replicating, or both. The CARA permits rapid evaluation of time- and concentration-dependent activity and identifies parameters to pursue by colony forming unit (CFU) assays.

There is an urgent need to discover and progress anti-infectives that shorten the duration of tuberculosis (TB) treatment. Mycobacterium tuberculosis, the ...

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Immunology and Infection

10.4K Views.  Weill Cornell Medical College. The charcoal agar resazurin assay (CARA) is a semi-quantitative, medium-throughput method to assess activity of test agents against mycobacteria that are replicating, non-replicating, or both. The CARA permits rapid evaluation of time- and concentration-dependent activity and identifies parameters to pursue by colony forming unit (CFU) assays. 

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

A Functional Whole Blood Assay to Measure Viability of Mycobacteria, using Reporter-Gene Tagged BCG or M.Tb (BCG lux/M.Tb lux)

Functional assays have long played a key role in measuring of immunogenicity of a given vaccine. This is conventionally expressed as serum bactericidal titers. Studies of serum bactericidal titers in response to childhood vaccines have enabled us to develop and validate cut-off levels for protective immune responses and such cut-offs are in routine use. No such assays have been taken forward into the routine assessment of vaccines that induce primarily cell-mediated immunity in the form of effector T cell responses, such as TB vaccines. In the animal model, the performance of a given vaccine candidate is routinely evaluated in standardized bactericidal assays, and all current novel TB-vaccine candidates have been subjected to this step in their evaluation prior to phase 1 human trials. The assessment of immunogenicity and therefore likelihood of protective efficacy of novel anti-TB vaccines should ideally undergo a similar step-wise evaluation in the human models now, including measurements in bactericidal assays.
Bactericidal assays in the context of tuberculosis vaccine research are already well established in the animal models, where they are applied to screen potentially promising vaccine candidates. Reduction of bacterial load in various organs functions as the main read-out of immunogenicity. However, no such assays have been incorporated into clinical trials for novel anti-TB vaccines to date.
Although there is still uncertainty about the exact mechanisms that lead to killing of mycobacteria inside human macrophages, the interaction of macrophages and T cells with mycobacteria is clearly required. The assay described in this paper represents a novel generation of bactericidal assays that enables studies of such key cellular components with all other cellular and humoral factors present in whole blood without making assumptions about their relative individual contribution. The assay described by our group uses small volumes of whole blood and has already been employed in studies of adults and children in TB-endemic settings. We have shown immunogenicity of the BCG vaccine, increased growth of mycobacteria in HIV-positive patients, as well as the effect of anti-retroviral therapy and Vitamin D on mycobacterial survival in vitro. Here we summarise the methodology, and present our reproducibility data using this relatively simple, low-cost and field-friendly model.
Note: Definitions/Abbreviations
BCG lux = M. bovis BCG, Montreal strain, transformed with shuttle plasmid pSMT1 carrying the luxAB genes from Vibrio harveyi, under the control of the mycobacterial GroEL (hsp60) promoter. 
CFU = Colony Forming Unit (a measure of mycobacterial viability).

A Functional Whole Blood Assay to Measure Viability of Mycobacteria, using Reporter-Gene Tagged BCG or M.Tb BCG lux/M.Tb lux

We describe an alternative approach to the enumeration of mycobacteria in vitro, which uses reporter-gene tagged mycobacteria instead of colony-forming units (CFU). &#x201C;Survival&#x201D; of organisms as well as host response-markers are measured simultaneously, providing a low-cost, versatile and functional system for studies of host/pathogen interactions in the context of tuberculosis.

Functional assays have long played a key role in measuring of immunogenicity of a given vaccine. This is conventionally expressed as serum bactericidal ...

A Microscopic Phenotypic Assay for the Quantification of Intracellular Mycobacteria Adapted for High-throughput/High-content Screening

Despite the availability of therapy and vaccine, tuberculosis (TB) remains one of the most deadly and widespread bacterial infections in the world. Since several decades, the sudden burst of multi- and extensively-drug resistant strains is a serious threat for the control of tuberculosis. Therefore, it is essential to identify new targets and pathways critical for the causative agent of the tuberculosis, Mycobacterium tuberculosis (Mtb) and to search for novel chemicals that could become TB drugs. One approach is to set&#160;up methods suitable for the genetic and chemical screens of large scale libraries enabling the search of a needle in a haystack. To this end, we developed a phenotypic assay relying on the detection of fluorescently labeled Mtb within fluorescently labeled host&#160;cells using automated confocal microscopy. This in vitro assay allows an image based quantification of the colonization process of Mtb&#160;into the host and was optimized for the 384-well microplate format, which is proper for screens of siRNA-, chemical compound- or Mtb mutant-libraries. The images are then processed for multiparametric analysis, which provides read&#160;out inferring on the pathogenesis of Mtb&#160;within host cells.

Here, we describe a phenotypic assay applicable to the High-throughput/High-content screens of small-interfering synthetic RNA (siRNA), chemical compound, and Mycobacterium tuberculosis mutant libraries. This method relies on the detection of fluorescently labeled Mycobacterium tuberculosis within fluorescently labeled host&#160;cell using automated confocal microscopy.

Despite the availability of therapy and vaccine, tuberculosis (TB) remains one of the most deadly and widespread bacterial infections in the world. Since ...

System for Efficacy and Cytotoxicity Screening of Inhibitors Targeting Intracellular Mycobacterium tuberculosis

Mycobacterium tuberculosis, the causative agent of tuberculosis (TB), is a leading cause of morbidity and mortality worldwide. With the increased spread of multi drug-resistant TB (MDR-TB), there is a real urgency to develop new therapeutic strategies against M. tuberculosis infections. Traditionally, compounds are evaluated based on their antibacterial activity under in vitro growth conditions in broth; however, results are often misleading for intracellular pathogens like M. tuberculosis since in-broth phenotypic screening conditions are significantly different from the actual disease conditions within the human body. Screening for inhibitors that work inside macrophages has been traditionally difficult due to the complexity, variability in infection, and slow replication rate of M. tuberculosis. In this study, we report a new approach to rapidly assess the effectiveness of compounds on the viability of M. tuberculosis in a macrophage infection model. Using a combination of a cytotoxicity assay and an in-broth M. tuberculosis viability assay, we were able to create a screening system that generates a comprehensive analysis of compounds of interest. This system is capable of producing quantitative data at a low cost that is within reach of most labs and yet is highly scalable to fit large industrial settings.

System for Efficacy and Cytotoxicity Screening of Inhibitors Targeting Intracellular Mycobacterium tuberculosis

We have developed a modular high-throughput screening system for discovering novel compounds against Mycobacterium tuberculosis, targeting intracellular and in-broth growing bacteria as well as cytotoxicity against the mammalian host cell.

Mycobacterium tuberculosis, the causative agent of tuberculosis (TB), is a leading cause of morbidity and mortality worldwide. With the increased spread ...

A High-throughput Compatible Assay to Evaluate Drug Efficacy against Macrophage Passaged Mycobacterium tuberculosis

The early drug development process for anti-tuberculosis drugs is hindered by the inefficient translation of compounds with in vitro activity to effectiveness in the clinical setting. This is likely due to a lack of consideration for the physiologically relevant cellular penetration barriers that exist in the infected host. We recently established an alternative infection model that generates large macrophage aggregate structures containing densely packed M. tuberculosis (Mtb) at its core, which was suitable for drug susceptibility testing. This infection model is inexpensive, rapid, and most importantly BSL-2 compatible. Here, we describe the experimental procedures to generate Mtb/macrophage aggregate structures that would produce macrophage-passaged Mtb for drug susceptibility testing. In particular, we demonstrate how this infection system could be directly adapted to the 96-well plate format showing throughput capability for the screening of compound libraries against Mtb. Overall, this assay is a valuable addition to the currently available Mtb drug discovery toolbox due to its simplicity, cost effectiveness, and scalability.

A High-throughput Compatible Assay to Evaluate Drug Efficacy against Macrophage Passaged Mycobacterium tuberculosis

New models and assays that would improve the early drug development process for next-generation anti-tuberculosis drugs are highly desirable. Here, we describe a quick, inexpensive, and BSL-2 compatible assay to evaluate drug efficacy against Mycobacterium tuberculosis that can be easily adapted for high-throughput screening.

The early drug development process for anti-tuberculosis drugs is hindered by the inefficient translation of compounds with in vitro activity to ...

An Automated Culture System for Use in Preclinical Testing of Host-Directed Therapies for Tuberculosis

Mycobacterium tuberculosis (Mtb), the causative agent of tuberculosis (TB), was the most significant infectious disease killer globally until the advent of COVID-19. Mtb has evolved to persist in its intracellular environment, evade host defenses, and has developed resistance to many anti-tubercular drugs. One approach to solving resistance is identifying existing&#160;approved drugs that will boost the host immune response to Mtb. These drugs could then be repurposed as adjunctive host-directed therapies (HDT) to shorten treatment time and help overcome antibiotic resistance.
Quantification of intracellular Mtb growth in macrophages is a crucial aspect of assessing potential HDT. The gold standard for measuring Mtb growth is counting colony-forming units (CFU) on agar plates. This is a slow, labor-intensive assay that does not lend itself to rapid screening of drugs. In this protocol, an automated, broth-based culture system, which is more commonly used to detect Mtb in clinical specimens, has been adapted for preclinical screening of host-directed therapies. The capacity of the liquid culture assay system to investigate intracellular Mtb growth in macrophages treated with HDT was evaluated. The HDTs tested for their ability to inhibit Mtb growth were all-trans Retinoic acid (AtRA), both in solution and encapsulated in poly(lactic-co-glycolic acid) (PLGA) microparticles and the combination of interferon-gamma and linezolid. The advantages of this automated liquid culture-based technique over the CFU method include simplicity of setup, less labor-intensive preparation, and faster time to results (5-12 days compared to 21 days or more for agar plates).

Rapid and efficient quantification of intracellular M. tuberculosis growth is crucial for pursuing improved therapies against tuberculosis (TB). This protocol describes a broth-based colorimetric detection assay using an automated liquid culture system to quantify Mtb growth in macrophages treated with candidate host-directed therapies.

Mycobacterium tuberculosis (Mtb), the causative agent of tuberculosis (TB), was the most significant infectious disease killer globally until the advent ...

High-Throughput Screening Assay for Mycobacterium abscessus Using Dual Reporters

Assay Development for High-Throughput Drug Screening Against Mycobacteria

Mycobacterium abscessus (Mab) infections are challenging to treat due to high intrinsic drug resistance, comparable to multidrug-resistant tuberculosis. Treatments are extremely ineffective and based on a multi-drug regimen, resulting in low patient compliance. Consequently, the scientific community is urged to identify new and effective drugs to treat these infections. One of the strategies employed to this end is drug repurposing - the process of identifying new therapeutic opportunities for existing drugs in the market, circumventing the time required to establish pharmacokinetic and safety profiles of new drugs. With most studies on drug development against Mab relying on traditional and time-consuming methods, an assay for high-throughput drug screening was developed against mycobacteria using an in house developed double-reporter strain of Mab. Using liquid-handling robotics, automated microscopy, and analysis, alongside in house developed double reporter strains, bacterial viability can be rapidly measured using two different readouts, luminescence and fluorescence, without adding reagents or performing any extra steps. This reduces time and variability between assays, a major advantage for high-throughput screenings. The described protocol was validated by screening a library of 1280 compounds. The obtained results were corroborated by the literature, with efficient detection of active compounds. Thus, this work fulfilled the aim of supplying the field with a new tool to help fight this extremely drug-resistant bacteria.

Author Spotlight: Scalable Drug Screening Protocol for Efficient Discovery of M. abscessus Treatments

This study developed an assay for high-throughput screening against Mycobacterium abscessus with a&#160;recently created double reporter strain, using fluorescence and luminescence to assess bacterial viability quickly. This protocol will be relevant for researchers aiming to screen new drugs against this drug-resistant bacteria.

Mycobacterium abscessus (Mab) infections are challenging to treat due to high intrinsic drug resistance, comparable to multidrug-resistant tuberculosis. ...

An Assay to Evaluate Drug Efficacy against a Mycobacterium tuberculosis Infection Model

Source: Schaaf, K., et al. <a href="https://app-jove-com.remotexs.ntu.edu.sg/v/55453">A High-throughput Compatible Assay to Evaluate Drug Efficacy against Macrophage Passaged Mycobacterium tuberculosis.</a> J. Vis. Exp. (2017)
This video demonstrates an assay to evaluate the efficacy of drugs against Mycobacterium tuberculosis (Mtb) infection. An in vitro infection model containing Mtb/macrophage aggregates is generated that mimics in vivo infection. Upon introducing suitable antibiotics, their efficacy is tested via resuzarin assay to monitor the survival of bacteria with increasing drug concentrations.

1. Culture Conditions for Green Fluorescent Protein Expressing M. tuberculosis mc26206 (Mtb-GFP)
NOTE: The M. tuberculosis H37Rv derived auxotroph strain ...

JoVE Encyclopedia of Experiments

Immunology

Immunodiagnostics

In Vitro and In Vivo Models

A Charcoal Agar Resazurin Assay to Evaluate Test Compound Activity Against Mycobacteria

Source: Gold, B. et al., <a href="https://app-jove-com.remotexs.ntu.edu.sg/v/54690">Visualization of the Charcoal Agar Resazurin Assay for Semi-quantitative, Medium-throughput Enumeration of Mycobacteria.</a> J. Vis. Exp. (2016)
This video showcases the Charcoal Agar Resazurin Assay (CARA) for evaluating the activity of antimicrobial compounds against Mycobacterium tuberculosis. CARA aids in assessing the efficacy of these compounds by gauging their impact on bacterial growth and distinguishing between bactericidal and bacteriostatic effects.

1. Setting Up Replicating and Non-replicating MIC90 Assays

	Inoculate M. tuberculosis, M. bovis BCG or M. smegmatis at an OD580 of 0.01-0.1 and expand to ...

Specialized Assays

A Charcoal Agar Resazurin Assay to Evaluate Test Compound Activity against Mycobacteria

Inoculate polypropylene round-bottom or conical centrifuge tubes containing 4 or 20 milliliters respectively of Middlebrook 7H9-ADN, or 7H9-OADC with M. smegmatis at an OD580 of 0.01 to 0.1. Incubate the M. smegmatis cultures at 37 degrees Celsius and 20% O2 with shaking, expanding the cultures to mid-log phase or an approximate OD580 of 0.5.
To set up a minimal inhibitory concentration style experiment under replicating and non-replicating conditions, distribute 200 microliters of cells in 7H9-ADN at an OD580 of 0.01 into all the wells of a clear-bottomed tissue culture-treated 96-well plate.
For the non-replicating assay, use PBS containing 0.02% tyloxapol to wash the cells twice and use non-replicating medium to resuspend the cells. Use non-replicating medium to dilute the cells to an OD580 of 0.1, and add sodium nitrite to a final concentration of 0.5 to 5 millimolar from a freshly prepared 1 molar stock.
Distribute 200 microliters of cells at an OD580 of 0.1 into all wells of a clear-bottomed tissue culture-treated 96-well plate. After preparing test agents according to the text protocol, add 2 microliters of test agent #1 into rows A through E, and 2 microliters of test agent #2 into rows E through H, and mix thoroughly.
For replicating assays, incubate M. smegmatis microplates at 37 degrees Celsius, 20% O2, and 5% CO2 for 1 to 48 hours. At the time points in which the CARA will be used as a readout, use a P200 multichannel pipette set at 50 to 75 microliters to carefully resuspend the well contents of the MIC90-style assay plate by pipetting up and down 5 to 10 times. Then, use the pipette tips to gently swirl the contents of the wells in a circular motion.
Transfer 10 microliters of the undiluted assay well contents to the corresponding wells of the CARA microplate, avoiding splashing during transfers, and ensuring that the 10-microliter aliquot is spotted into the middle of the CARA microplate wells. With plate tape, bind stacks of CARA microplates, and then, place them into a resealable plastic bag. Incubate the M. smegmatis CARA microplates at 37 degrees Celsius with 20% O2 for one to two days for replicating plates and for two to three days for non-replicating plates.
When a film of bacterial growth, or larger macroscopic colonies are visible in the negative control wells, use a single set of 12 P200 tips with a multichannel pipette to dispense 40 microliters of sterile PBS along the side of the wells, and allow the PBS to distribute across the top of the agar bacterial microcolonies.
Prepare CARA developing reagent by mixing 5 milligrams of resazurin and 50 milliliters of 5% Tween-80 in PBS. Add 50 microliters of freshly prepared CARA developing reagent to each well of the CARA microplate. Then, rock the plates back and forth a few times to help distribute the reagent across the agar and bacterial mat in each well. Place the plates into a resealable plastic bag, and incubate at 37 degrees Celsius for at least 30 minutes for M. smegmatis.
Prior to reading fluorescence, place CARA microplates in a biosafety hood for 15 minutes at room temperature with the lids removed. When using BSL3 spectrophotometers outside of a biosafety cabinet, adhere an optical quality PCR sticker over the plate, and use a soft paper towel to seal tightly by pressing gently on the sticker surface. Determine the fluorescence via top read with excitation at 530 nanometers and emission at 590 nanometers.

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Evaluating the Effectiveness of a Test Compound against Mycobacteria in Broth

To carry out a resazurin assay, grow M. tuberculosis in 7H9ADST to mid-log phase. Dilute the culture with 7H9ADST to an OD600 of 0.01. Use 7H9ADST to dilute the compounds to two times the testing concentrations, and aliquot 100 microliters of each diluted compound into each well of a clear 96-well plate.
Transfer 100 microliters of the diluted bacterial suspension into each well. Incubate the plates at 37 degrees Celsius in a humidified incubator for 5 days. Dissolve 10 milligrams of resazurin in 100 milliliters of deionized water, and filter-sterilize the solution. Add 30 microliters of resazurin solution to the wells. Then, incubate the cells for 48 hours.
Bacterial growth is indicated by a color conversion from blue to pink. Carry out quantitative analysis according to the text protocol.

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

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A Charcoal Agar Resazurin Assay to Evaluate Test Compound Activity Against Mycobacteria

A Charcoal Agar Resazurin Assay to Evaluate Test Compound Activity against Mycobacteria

Evaluating the Effectiveness of a Test Compound against Mycobacteria in Broth