This work was supported by a grant from the National Institute on Drug Abuse (U01 DA041613) to TFCM and RRHA.

1. Starvation plate preparation
<ol>
	<li>Weigh out 1.5 g of agarose into a 250 mL glass beaker.</li>
	<li>Add 100 mL of distilled H2O to the beaker.</li>
	<li>Microwave intermittently until agarose is fully molten. 
	NOTE: Observe the beaker since the agarose is prone to boiling over.</li>
	<li>Pour the molten agarose into a reagent trough and dispense 80 &#181;L of molten agarose into each well of a 96-well microplate using a multichannel pipette. Allow plates to cure while covered at room temperature. Refrigerate the leftover agarose for up to a week in a sealed bag and re-melt it for making additional plates.</li>
</ol>
2. Fly sorting and starvation
<ol>
	<li>Prepare couplers by inserting barrier strips into the barrier strip channels. If barrier strips are too loose, coil them around the finger to give them curvature to hold them in the channels.</li>
	<li>Affix the coupler to a starvation plate. Do not use the coupler to manipulate the plate since the coupler may slip off. Ensure that the couplers are correctly oriented (i.e., ensure the angled corner of the coupler matches the angled corner of the microplate).</li>
	<li>Under CO2 anesthesia (Table of Materials), sort 3-5-day old flies. Load individual flies by column into the starvation plate. 
	NOTE: Although flies are loaded by column, it is recommended to distribute groups of samples down rows of the plate rather than down columns (see Figure 4 for plate layout example).</li>
	<li>Close each column as it fills by adjusting its barrier strip to the closed position.</li>
</ol>
<img alt="Figure 4" class="xfigimg" src="/files/ftp_upload/62771/62771fig04.jpg" /> 
Figure 4: Representative Starvation Plate Layout. The diagram shows&#160;the organization of evaporation controls and male and female flies in a 96-well plate used in this study. Alternative configurations, including alternating rows of males and females with evaporation controls in rows A and H, can also be used. <a href="https://jove.unicartagenaproxy.elogim.com/files/ftp_upload/62771/62771fig04large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<ol start="5">
	<li>Carefully record the sample layout within the microplate. Once the starvation plate is filled, allow the flies to recover spontaneously after removing the CO2 and starve them for 6 h starting from their initial anesthetization time.</li>
</ol>
3. Liquid food preparation
NOTE: Make liquid food fresh every day.
<ol>
	<li>Prepare a 10 mg/mL of dye stock solution of FD&#38;C Blue #1 in distilled H2O. 
	NOTE: This may be stored at room temperature for up to 6 months.</li>
	<li>Prepare 10 mL of liquid food (4% sucrose, 1% yeast extract, 40 &#181;g/mL of FD&#38;C Blue #1) in a 15 mL conical tube by dissolving 0.4 g of sucrose and 0.1 g of yeast extract in 10 mL of distilled H2O. Vortex the tube until the solids fully dissolve. Add 40 &#181;L of dye stock solution and invert the tube repeatedly to homogenize the solution.</li>
	<li>Transfer the liquid food into a 10 mL syringe tipped with a 0.45 &#181;m filter. Filter ~1.5 mL of the solution at a time into a 1.7 mL microcentrifuge tube. Set aside the syringe containing the solution and filter the additional solution as needed during feeder plate preparation.</li>
</ol>
4. Feeder plate preparation
NOTE: Handle the feeder plates gently after filling to prevent the formation of bubbles or droplets in the well that could influence the absorbance readings.
<ol>
	<li>Prepare a feeder plate by sealing the bottom of a 1536-well microplate with a sealing film. Use a sealing paddle to adhere to the film thoroughly. Trim excess film off the left and right edges with a razor blade.</li>
	<li>Dispense 10 &#181;L of the filtered liquid food column-wise (see Figure 5 for illustration) into the appropriate wells of the 1536-well microplate. Dispense into the upper-left-hand well for each cluster of four wells (see Figure 5 for illustration).</li>
</ol>
<img alt="Figure 5" class="xfigimg" src="/files/ftp_upload/62771/62771fig05.jpg" /> 
Figure 5: Fill order and well location for the 1536-well feeder plate. The diagram illustrates step 4.2 of the protocol. Arrows show the order in which the feeding solution is introduced in the feeder plate one column at a time from column 1 through 12. Sample B1 is magnified to show an example of the location of feeding solutions for 1-choice and 2-choice assays. <a href="https://jove.unicartagenaproxy.elogim.com/files/ftp_upload/62771/62771fig05large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<ol start="3">
	<li>Once all the wells are filled, apply a sealing film to the top of the plate. Use a sealing paddle to adhere to the film thoroughly. Trim excess film off the left and right edges with a razor blade. Repeat for the desired number of plates.</li>
	<li>Centrifuge the plates at 200 x g for 10 s to settle the fluid. Do not allow the plate to be chilled since this can cause condensation to build up in the wells, obscuring absorbance readings.</li>
</ol>
5. Exposure
<ol>
	<li>Once the flies are ready for the consumption assay, perforate the wells on the top surface of the plate with the needle probe tool equipped with a 0.25 mm diameter needle. Use the same order to perforate as was used when dispensing the solutions. Flip the plate and perforate the wells on the bottom. Wipe off the needle between solutions to prevent cross-contamination. Be careful not to touch the perforations as this wicks the solution from the wells.</li>
	<li>Read the plate&#39;s absorbance at 630 nm without a lid.</li>
	<li>Place an internal lid on the top sealing film to ensure that the condensation rings encircle the perforated wells. Place the external lid on the plate.</li>
	<li>Place the feeder plate face-up on the coupler such that the guides align the appropriate holes of the feeder plate and starvation plate. Ensure that the coupler and plates are correctly oriented (i.e., ensure the angled corner of the coupler and the plates match). Wrap elastic bands around the top and bottom plates to hold the coupler together. Check for alignment and gaps between the feeder plate and coupler.</li>
	<li>Once all the feeder plates are loaded onto the couplers, open the wells for the plates by adjusting the barrier strips on the coupler. Place the coupler/plate assemblies in the secondary container. Each secondary container can accommodate up to six assemblies.</li>
	<li>Place the lower half of a pipette box containing soaked paper towels into each secondary container to provide humidity. Close the lid of the secondary containers and transfer them to a controlled environment (25 &#176;C, humidity controlled, 12 h light:dark cycles). Allow the flies to consume for 22 h.</li>
	<li>After the 22 h exposure, check each plate for dead flies and update the plate layout accordingly. After all the plates are checked, anesthetize the flies en masse by pumping CO2 inside the secondary container. After ~60 s, ensure that all the flies are immobilized. Gently tamp the flies into the starvation plate and replace the plastic barrier strips. Remove the feeder plates for reading.</li>
	<li>Re-read the plate&#39;s absorbance at 630 nm. Repeat until all plates have been read.</li>
</ol>
6. Data analysis
NOTE: Analysis can be performed with the investigator&#39;s preferred software package.
<ol>
	<li>Omit any flies that died during the 22 h exposure.</li>
	<li>For each well, calculate the volume consumed as: 
	<img alt="Equation 2" src="/files/ftp_upload/62771/62771eq02.jpg" /> 
	C -&#160;Volume Consumed (&#181;L) 
	V - Initial Well Volume (i.e., 10 &#181;L) 
	ABS0 - Pre-Exposure Absorbance 
	ABS1 - Post-Exposure Absorbance 
	NOTE: Consumption is denoted as a positive volume in the calculation.</li>
	<li>To account for evaporation, subtract the mean evaporation volume from fly consumption values within respective plates. For 2-choice/preference testing, adjust every well by its respective solution, e.g., adjust &#34;choice 1&#34; wells by &#34;choice 1&#34; in the evaporation controls.</li>
	<li>After adjusting for evaporation, drop any samples with a consumption value less than zero.</li>
	<li>For 2-choice testing, calculate the preference for each well as: 
	<img alt="Equation 3" src="/files/ftp_upload/62771/62771eq03.jpg" /> 
	P - Preference Index (positive direction indicates preference) 
	FA - Volume of Liquid Food Consumed Containing Additive (Choice 2) 
	FN -&#160;Volume of Normal Liquid Food Consumed (Choice 1)</li>
</ol>
7. Microplate and coupler washing protocol.
NOTE: Take care to prevent damage to the bottoms of the microplates, as damage can affect sealing.
<ol>
	<li>Remove the films and labels from the 1536-well microplates. Separate the couplers and barrier strips. Place the barrier strips in a sealable container, such as a bottle. Wash the barrier strips by vigorously shaking in a series of warm tap water, mild detergent solution, warm tap water, and then distilled H2O.</li>
	<li>Rinse 1536-well microplates and couplers under warm tap water. For microplates, run tap water through each microplate&#39;s wells to clear as much solution and debris as possible. If needed, use a pipette tip to dislodge debris; do not use metal or glass utensils on the plates.</li>
	<li>Cover each plate and coupler with a mild detergent solution (e.g., 1% v/v Aquet). For the plates, scrub the surfaces with a gloved hand. For the couplers, use a brush.</li>
	<li>Rinse each plate thoroughly with tap water, and then with distilled H2O. Ensure that the wells are specifically rinsed out under the water flow.</li>
	<li>Allow the plates and couplers to air dry covered at room temperature. Store in a clean storage bin until use. 
	NOTE: Never handle the 1536-well microplates without gloves. Residual oils from the skin can hinder sealing, leading to well leakage and evaporation.</li>
</ol>

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The authors have no conflicts of interest to disclose.

The study describes a novel protocol for quantifying consumption in Drosophila: the Microplate Feeder Assay (MFA). In this assay, flies consume from sealed wells of a 1536-well microplate through controlled-size perforations (Figure 1, Figure 2; Supplementary Video S.1). Since liquid food is dyed and provided via microplate, measurements of the optical absorbance of the food can be obtained using a microplate spectrophotometer (Figure 3). In this manner, consumption is determined by comparing the absorbance before and after consumption, and then applying this proportion to the known volume dispensed prior to consumption. This was verified empirically by measuring the absorbance of different volumes of the dyed medium (Figure 3B).
To develop this assay, a device was needed that could leverage the absorbance-based quantification of consumption. Testing flies in a microplate format is appealing because it complements the microplate used to dispense food and allows for flexibility in selecting from multiple plate formats (e.g., 6-, 12-, 48-, or 96-well formats) by adjusting the coupler geometry. A 96-well microplate format was chosen to allow for individual fly culture.
The 3D printed device (Figure 1) precisely orients the 1536-well feeder plate with the 96-well culture plate, giving each fly access to up to 4 wells of the feeder plate for consumption. Furthermore, to provide adequate time for distributing flies into the housing plate and to control assay initiation, the device includes toggling barrier strips containing the flies in their respective wells and preventing breaches. The files needed to procure or modify these parts are provided (Supplementary Files S.2-S.3), as well as the necessary fabrication instructions for the relevant pieces (Supplementary File S.4).
The MFA provides a simple high throughput method that complements more elaborate methods to monitor Drosophila feeding behavior18,21,22. The MFA offers multiple advantages over other methods used to quantify food intake. The throughput is increased by quantifying consumption using a plate reader. This eliminates manual measurements and obviates manual data entry. Data are also amenable to programmatic extraction and processing. In addition, the higher throughput increases the feasible number of biological replicates, particularly compared to communal feeder designs, which substantially increases the power to detect small differences in consumption. Using the MFA, a single experimenter can quantify the consumption or preference of over 500 flies per overnight run of the assay. By overlapping runs of the assay, over 2,000 flies can be tested in a 5-day period. Lastly, there are long-term cost savings due to the reusability of microplates and couplers (Supplementary File S.5). Using the MFA, the estimated cost per assay can be as low as $14.80, with a $127.60 up-front cost for the equipment. Using the classic CApillary FEeder (CAFE) assay, which requires costly precision microcapillaries, the estimated cost per assay for a comparable number of replicates is $46.08. Thus, while there is an upfront investment in acquiring the necessary equipment, the reduction in recurring costs can lead to substantial savings, particularly in instances where repeated testing is performed.
As with all assays, the MFA has certain limitations. Chiefly, it requires access to a microplate spectrophotometer capable of reading 1536-well microplates. Additionally, the reliance on absorbance measurements for quantification makes the method susceptible to optical interference. This manifests as negative consumption values for a small subset of samples tested. Nutrients, drugs, pharmaceuticals, or toxins of interest must also be water-soluble to be compatible with the assay.
Despite its limitations, this method offers a high throughput method of quantifying consumption behaviors in Drosophila. Furthermore, the coupling device could be easily modified to accept many plate formats, allowing it to accommodate a variety of insect species.

Drosophila melanogaster has seen wide use as a genetic model organism to study the biological underpinnings of food intake and traits associated with consumption1. It is estimated that 65% of human disease-causing genes have functional homologs in flies, with a significant proportion of those being expressed in functionally equivalent tissues between flies and humans2. Moreover, D. melanogaster&#39;s size, short intergenerational time, simple maintenance, and genetic tractability make it an attractive model for studies on the consumption of nutrients3,4 and toxicological and pharmacological effects of a variety of substances, including insecticides5, pollutants6, pharmaceuticals7, and drugs of abuse8,9,10.
In many cases, the study of such traits requires precise quantification of consumption. Methods for quantifying consumption are diverse and include the CApillary FEeder (CAFE) assay11, the MAnual FEeding (MAFE) assay12, Proboscis Extension Response (PER) assay13, tracer dye extraction14,15, oligonucleotide tracer extraction16, and radio-isotope extraction5,17. Recent efforts have focused on enhancing the throughput of these assays, as in the Expresso assay18 or the plate-based Whole Animal Feeding FLat (WAFFL) system19. Despite their utility, these assays can be complicated, costly, or labor-intensive, hindering their use in high throughput studies.
<img alt="Figure 1" class="xfigimg" src="/files/ftp_upload/62771/62771fig01.jpg" /> 
Figure 1: Components of the Microplate Feeder Assay. (A) 3D rendering of the assembled microplate feeder assay. The 1536-well microplate is oriented by the 3D-printed coupler such that each well of the lower 96-well microplate has access to four wells of the upper 1536-well microplate. Access to the wells can be controlled by adjusting the position of barrier strips slotted through the coupler. (B) A graphical representation of each well of the microplate feeder assay. Consumption solutions are retained in each well using a sealing film that has been perforated to allow access by the fly. <a href="https://jove.unicartagenaproxy.elogim.com/files/ftp_upload/62771/62771fig01large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 2" class="xfigimg" src="/files/ftp_upload/62771/62771fig02.jpg" /> 
Figure 2: Overview of the procedures in the Microplate Feeder Assay. The figure shows a flow diagram that corresponds to steps 4.1-5.8 of the protocol. <a href="https://jove.unicartagenaproxy.elogim.com/files/ftp_upload/62771/62771fig02large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
To overcome these hurdles, the Microplate Feeder Assay (MFA; Figure 1) was developed. In this assay, flies are housed individually in 96-well microplates. Each microplate is coupled to a 1536-well microplate using a custom, 3D-printed device. The device precisely orients the two plates such that each fly in its respective well of the 96-well plate has access to 4 wells of the 1536-well microplate. By using a bottomless 1536-well plate and sealing films, solutions are dispensed into select wells and perforated with precise 0.25 mm diameter needles to provide access to the flies. Critically, allowing consumption directly from a microplate allows for immediate absorbance-based measurements using a microplate reader. A dilute tracer dye is incorporated into the consumption medium, and the change in absorbance after exposure is used to determine the volume consumed (Figure 2 and Figure 3). Since the liquid in each well approximates a column of fluid, volumetric differences will manifest as differences in the height of the column. (Figure 3A) According to the Beer-Lambert law20:
<img alt="Equation 1" src="/files/ftp_upload/62771/62771eq01.jpg" />
where A is the absorbance,&#160;&#949; is the molar absorption coefficient for the attenuating analyte, l is the optical path length, and c is the concentration of the attenuating analyte. Thus, with constant molar absorption coefficient and concentration, changes in absorbance are due solely to changes in the optical light path, i.e., the fluid level within a given well. By measuring absorbance before and after exposure, the proportional change in absorbance reflects the proportional change in volume (Figure 3B).
<img alt="Figure 3" class="xfigimg" src="/files/ftp_upload/62771/62771fig03.jpg" /> 
Figure 3: Absorbance-based quantification of well volume. (A) Incident light of known input intensity (I0) traverses each well. Attenuation of light at different fill volumes yields different output intensities (I), exhibiting a linear relationship between volume and absorbance. (B) Empirical measurement of absorbance vs. volume. <a href="https://jove.unicartagenaproxy.elogim.com/files/ftp_upload/62771/62771fig03large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
Based on the change in volume, the amount of any ingested compound can be calculated from its known concentration in the feeding solution. The parts needed for the assay are low in cost and have a high degree of reusability, substantially reducing the recurring cost of the assay. Thus, this procedure offers an affordable, high throughput method of precisely quantifying consumption.

<table><tbody><tr><td>0.25 mm Diameter Needles</td><td>Rave Scientific</td><td>RS-MN-52-001012</td><td></td></tr><tr><td>0.45 &amp;micro;m Syringe Filters</td><td>Olympus Plastics</td><td>25-245</td><td></td></tr><tr><td>10 mL Disposable Syringe</td><td>EXELINT</td><td>26200</td><td></td></tr><tr><td>Agarose</td><td>Fisher Scientific</td><td>BP1600</td><td></td></tr><tr><td>Barrier Strips (Laser Cut)</td><td>Ponoko</td><td>-</td><td>Material: clear PETG, 0.5mm thickness; Supplementary File:</td></tr><tr><td>Centrifuge 5810 R</td><td>Eppendorf</td><td>22625501</td><td></td></tr><tr><td>Centrifuge Rotor A-4-62 with micro-titer plate buckets</td><td>Eppendorf</td><td>22638041</td><td></td></tr><tr><td>FD&amp;amp;C Blue #1</td><td>Spectrum Chemical Mfg Corp</td><td>FD110</td><td></td></tr><tr><td>Film Sealing Paddle</td><td>Fisher Scientific</td><td>50-563-280</td><td></td></tr><tr><td>Flystuff Flypad</td><td>Genesee Scientific</td><td>#59-114 and #59-119</td><td>CO&lt;sub&gt;2 &lt;/sub&gt;Anesthesia: The Flypads&amp;nbsp; come in two sizes, either of which is appropriate</td></tr><tr><td>Microplate Coupler (3D Printed)</td><td>Shapeways</td><td>-</td><td>Material: Multi Jet Fusion nylon (MJF PA12); Supplementary File:</td></tr><tr><td>Microplate Lids</td><td>Greiner Bio-One</td><td>656170</td><td></td></tr><tr><td>Molecular Devices SpectraMax iD5</td><td>Molecular Devices</td><td>-</td><td>Any microplate reader with 1536-well resolution will do.</td></tr><tr><td>Needle Probe Holder</td><td>Rave Scientific</td><td>RS-MN-52-001000</td><td></td></tr><tr><td>Polyester Sealing Film</td><td>Excel Scientific, Inc.</td><td>100-SEAL-PLT</td><td></td></tr><tr><td>Polystyrene 96-well microplates</td><td>Greiner Bio-One</td><td>655101</td><td></td></tr><tr><td>Polystyrene, Bottomless, 1536-well microplates</td><td>Greiner Bio-One</td><td>783000</td><td>Made to Order; allow for adequate lead time when purchasing.</td></tr><tr><td>Rubber Bands</td><td></td><td></td><td></td></tr><tr><td>Sucrose</td><td>Sigma</td><td>S7903</td><td></td></tr><tr><td>Weather Stripping</td><td></td><td></td><td>1/2&quot; x 1/8&quot; High Density Self Adhesive Neoprene Rubber</td></tr><tr><td>Yeast Extract</td><td>Fisher Scientific</td><td>BP1422</td><td></td></tr></tbody></table>

a high throughput microplate feeder assay for quantification of consumption in drosophila

Quantifying food intake in Drosophila is used to study the genetic and physiological underpinnings of consumption-associated traits, their environmental factors, and the toxicological and pharmacological effects of numerous substances. Few methods currently implemented are amenable to high throughput measurement. The Microplate Feeder Assay (MFA) was developed for quantifying the consumption of liquid food for individual flies using absorbance. In this assay, flies consume liquid food medium from select wells of a 1536-well microplate. By incorporating a dilute tracer dye into the liquid food medium and loading a known volume into each well, absorbance measurements of the well acquired before and after consumption reflect the resulting change in volume (i.e., volume consumed). To enable high throughput analysis with this method, a 3D-printed coupler was designed that allows flies to be sorted individually into 96-well microplates. This device precisely orients 96- and 1536-well microplates to give each fly access to up to 4 wells for consumption, thus enabling food preference quantification in addition to regular consumption. Furthermore, the device has barrier strips that toggle between open and closed positions to allow for controlled containment and release of a column of samples at a time. This method enables high throughput measurements of consumption of aqueous solutions by many flies simultaneously. It also has the potential to be adapted to other insects and to screen consumption of nutrients, toxins, or pharmaceuticals.

To determine whether any correlations exist among the wells of individual plates, the evaporation was quantified for every well (n = 96 wells/plate for three plates). Evaporation was found to be -0.036 &#181;L &#177; 0.003 &#181;L (mean &#177; SEM throughout). (Figure 6A) Pearson correlations were calculated to evaluate trends between evaporation and well locations. The correlation coefficient (Figure 6B,C) for evaporation versus rows was -0.04 (p = 0.4949) and for evaporation vs columns was -0.23 (p = 0.0001). Groups were subsequently distributed among columns to mitigate the mild but statistically significant correlations across columns.
<img alt="Figure 6" class="xfigimg" src="/files/ftp_upload/62771/62771fig06.jpg" /> 
Figure 6: Evaporation in the MFA. (A) Density distribution of evaporation changes with mean &#177; SD indicated by the dashed line. Correlations between evaporation and rows (B) or columns (C) with the Pearson correlation coefficient and p-value as indicated. <a href="https://jove.unicartagenaproxy.elogim.com/files/ftp_upload/62771/62771fig06large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
To establish the validity of the protocol, consumption was quantified for 3-5-day old Canton-S B flies (n = 36/sex/plate and n = 24 evaporation controls/plate for three plates) (Figure 7). Evaporation among the control wells was significantly different from zero (-0.030 &#181;L &#177; 0.006 &#181;L, p = 4.81 x 10-6; one sample t-test vs zero). Two samples were omitted (both male) from the dataset, one due to death during the overnight exposure and the other due to negative consumption value following adjustment for evaporation. This yielded a &#62; 99% sample retention rate.
<img alt="Figure 7" class="xfigimg" src="/files/ftp_upload/62771/62771fig07.jpg" /> 
Figure 7: Consumption quantification using the MFA. (A) Consumption was visualized using a custom fabricated glass chamber. Flies were observed drinking from perforated wells and exhibited blue abdominal staining following ingestion of the dyed solution. See also Supplementary Video S.1. (B) Consumption values (mean &#177; SEM) among evaporation controls, male flies, and female flies. Pairwise post hoc t-test with unequal variance was performed for statistical comparisons, with significance indicated by bars. <a href="https://jove.unicartagenaproxy.elogim.com/files/ftp_upload/62771/62771fig07large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
Subsequently, an Analysis of Variance (ANOVA) model was constructed as described by Y = &#181; + S + P + SxP + e, with Y as the group mean, &#181; as the overall mean, S as the fixed effect of sex, P as the fixed effect of plate, SxP as the interaction between Sex and Plate, and e as the residual variability. ANOVA showed no significant plate-to-plate variability (p = 0.671) or sex-specific interactions with plates (p = 0.104) for consumption, while sex alone significantly contributed to the observed variation in consumption (p = 4.17 x 10-18). A post hoc t-test showed that males consumed significantly less than females (0.500 &#181;L &#177; 0.017 &#181;L vs 0.811 &#181;L &#177; 0.028 &#181;L, p = 1.13 x 10-17, two sample t-test with unequal variance).
To demonstrate that the assay can be used for two-choice preference quantification, flies were given a choice between a 4% sucrose solution with 1% yeast extract and a 4% sucrose solution supplemented with 15% ethanol and 1% yeast extract. Both males and females showed overwhelming preference for the solution with ethanol and yeast extract with preference indices of 0.974 &#177; 0.026 for males and 0.876 &#177; 0.06 for females (average &#177; SEM) (Figure 8).
<img alt="Figure 8" class="xfigimg" src="/files/ftp_upload/62771/62771fig08.jpg" /> 
Figure 8: Preference quantification using the MFA. Consumption of 4% sucrose versus 4% sucrose supplemented with 15% ethanol and yeast extract for male and female flies (n = 33 for each sex). Male flies consumed more of the ethanol solution than the control sucrose solution (0.511 &#181;L &#177; 0.029 &#181;L versus&#160;0.00 &#181;L &#177; 0.017 &#181;L; p = 4.06e-10; two-sample t-test). Female flies also consumed more ethanol solution than the control sucrose solution (0.939 &#181;L &#177; 0.044 &#181;L versus 0.132 &#181;L &#177; 0.044 &#181;L; p = 7.38e-17; two-sample t-test). <a href="https://jove.unicartagenaproxy.elogim.com/files/ftp_upload/62771/62771fig08large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
Supplementary Video S.1: The video shows a fly feeding from the perforated well and accumulating blue abdominal staining while ingesting the dyed solution. A still image is shown in Figure 7A. <a href="https://jove.unicartagenaproxy.elogim.com/files/ftp_upload/62771/JoVEJoVE_Review-Supplementary_Video_S.1.mp4" target="_blank">Please click here to download this video.</a>
Supplementary File S.2: Microplate Feeder Assay Coupler. This is a 3D-printable construct of the coupler used in the MFA. Printing material Nylon PA12 was used for the MFA. <a href="https://jove.unicartagenaproxy.elogim.com/files/ftp_upload/62771/Supplementary_File_S.2.STL" target="_blank">Please click here to download this file.</a>
Supplementary File S.3: Microplate Feeder Assay Barrier Strip. This contains the design of the plastic barrier strips used to toggle exposure of flies to the feeder plate. A single coupler can utilize up to twelve barrier strips. <a href="https://jove.unicartagenaproxy.elogim.com/files/ftp_upload/62771/Supplementary_File_S.3.tif" target="_blank">Please click here to download this file.</a>
Supplementary File S.4: Unpacking and fabrication instructions for the Microplate Feeder Assay. Instructions are included for unpacking the coupler and the barrier strips. Fabrication instructions are included for the inner lid, outer lid, and secondary container used to limit evaporation during exposure. <a href="https://jove.unicartagenaproxy.elogim.com/files/ftp_upload/62771/Supplementary_File_S.4.docx" target="_blank">Please click here to download this file.</a>
Supplementary File S.5:Cost comparison of the Microplate Feeder Assay (MFA) and a 1-choice single fly CApillary FEeder (CAFE) assay. Testing 72 flies/sex for a single line would require two sets of MFA equipment (couplers + plates + barrier strips), while the CAFE would only need 1 capillary for each culture vial. Despite the large difference in initial investment for the MFA, the large difference in recurring costs ($14.80 vs $46.08, respectively) would allow for the up-front costs to be recovered after testing only 4 lines (break-even point). <a href="https://jove.unicartagenaproxy.elogim.com/files/ftp_upload/62771/Supplementary_File_S.5.xlsx" target="_blank">Please click here to download this file.</a>

Watch this Scientific Journal Video about A High Throughput Microplate Feeder Assay for Quantification of Consumption in Drosophila at JoVE.com

A High Throughput Microplate Feeder Assay for Quantification of Consumption in Drosophila

The microplate feeder assay offers an economical, high throughput method for quantifying liquid food consumption in Drosophila. A 3D-printed device connects a 96-well microplate in which flies are housed to a 1536-well microplate from which flies consume a feeding solution with a tracer dye. The solution volume decline is measured spectrophotometrically.

A High Throughput Microplate Feeder Assay for Quantification of Consumption in Drosophila

Quantifying food intake in Drosophila is used to study the genetic and physiological underpinnings of consumption-associated traits, their environmental ...

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Universidad de Cartagena UDEC

Research

JoVE Journal

Behavior

3.2K Views.  Clemson University. The microplate feeder assay offers an economical, high throughput method for quantifying liquid food consumption in Drosophila. A 3D-printed device connects a 96-well microplate in which flies are housed to a 1536-well microplate from which flies consume a feeding solution with a tracer dye. The solution volume decline is measured spectrophotometrically. 

Video: A High Throughput Microplate Feeder Assay for Quantification of Consumption in Drosophila

High Fat Diet Feeding and High Throughput Triacylglyceride Assay in Drosophila Melanogaster

Heart disease is the number one cause of human death worldwide. Numerous studies have shown strong connections between obesity and cardiac malfunction in humans, but more tools and research efforts are needed to better elucidate the mechanisms involved. For over a century, the genetically highly tractable model of Drosophila has been instrumental in the discovery of key genes and molecular pathways that proved to be highly conserved across species. Many biological processes and disease mechanisms are functionally conserved in the fly, such as development (e.g., body plan, heart), cancer, and neurodegenerative disease. Recently, the study of obesity and secondary pathologies, such as heart disease in model organisms, has played a highly critical role in the identification of key regulators involved in metabolic syndrome in humans.
Here, we propose to use this model organism as an efficient tool to induce obesity, i.e., excessive fat accumulation, and develop an efficient protocol to monitor fat content in the form of TAGs accumulation. In addition to the highly conserved, but less complex genome, the fly also has a short lifespan for rapid experimentation, combined with cost-effectiveness. This paper provides a detailed protocol for High Fat Diet (HFD) feeding in Drosophila to induce obesity and a high throughput triacylglyceride (TAG) assay for measuring the associated increase in fat content, with the aim to be highly reproducible and efficient for large-scale genetic or chemical screening. These protocols offer new opportunities to efficiently investigate regulatory mechanisms involved in obesity, as well as provide a standardized platform for drug discovery research for rapid testing of the effect of drug candidates on the development or prevention of obesity, diabetes and related metabolic diseases.

High Fat Diet Feeding and High Throughput Triacylglyceride Assay in Drosophila Melanogaster

This is a high fat diet feeding protocol to induce obesity in Drosophila, a model for understanding fundamental molecular mechanisms implicated in lipotoxicity. It also provides a high throughput triacylglyceride assay for measuring fat accumulation in Drosophila and potentially other (insect) models under various dietary, environmental, genetic or physiological conditions.

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Genetics

Combining Quantitative Food-intake Assays and Forcibly Activating Neurons to Study Appetite in Drosophila

Food consumption is under the tight control of the brain, which integrates the physiological status, palatability, and nutritional contents of the food, and issues commands to start or stop feeding. Deciphering the processes underlying the decision-making of timely and moderate feeding carries major implications in our understanding of physiological and psychological disorders related to feeding control. Simple, quantitative, and robust methods are required to measure the food ingestion of animals after experimental manipulation, such as forcibly increasing the activities of certain target neurons. Here, we introduced dye-labeling-based feeding assays to facilitate the neurogenetic study of feeding control in adult fruit flies. We review available feeding assays, and then describe our methods step-by-step from setup to analysis, which combine thermogenetic and optogenetic manipulation of neurons controlling feeding motivation with dye-labeled food intake assay. We also discuss the advantages and limitations of our methods, compared with other feeding assays, to help readers choose an appropriate assay.

Combining Quantitative Food-intake Assays and Forcibly Activating Neurons to Study Appetite in Drosophila

Quantitative food-intake assays with dyed food provide a robust and high-throughput means to evaluate feeding motivation. Combining the food consumption assay with thermogenetic and optogenetic screens is a powerful approach to investigate the neural circuits underlying appetite in adult Drosophila melanogaster.

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A Single-fly Assay for Foraging Behavior in Drosophila

For many animals, hunger promotes changes in the olfactory system in a manner that facilitates the search for appropriate food sources. In this video article, we describe an automated assay to measure the effect of hunger or satiety on olfactory dependent food search behavior in the adult fruit fly Drosophila melanogaster. In a light-tight box illuminated by red light that is invisible to fruit flies, a camera linked to custom data acquisition software monitors the position of six flies simultaneously. Each fly is confined to walk in individual arenas containing a food odor at the center. The testing arenas rest on a porous floor that functions to prevent odor accumulation. Latency to locate the odor source, a metric that reflects olfactory sensitivity under different physiological states, is determined by software analysis. Here, we discuss the critical mechanics of running this behavioral paradigm and cover specific issues regarding fly loading, odor contamination, assay temperature, data quality, and statistical analysis.

A Single-fly Assay for Foraging Behavior in Drosophila

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Neuroscience

High Throughput Assay to Examine Egg-Laying Preferences of Individual Drosophila melanogaster

Recently, egg-laying preference of Drosophila has emerged as a genetically tractable model to study the neural basis of simple decision-making processes. When selecting sites to deposit their eggs, female flies are capable of ranking the relative attractiveness of their options and choosing the &#34;greater of two goods.&#34; However, most egg-laying preference assays are not practical if one wants to take a systematic genetic screening approach to search for the circuit basis underlying this simple decision-making process, as they are population-based and laborious to set up. To increase the throughput of studying of egg-laying preferences of single females, we developed custom chambers that each can simultaneously assay egg-laying preferences of up to thirty individual flies as well as a protocol that ensures each female has a high egg-laying rate (so that their preference is readily discernable and more convincing). Our approach is simple to execute and produces very consistent results. Additionally, these chambers can be equipped with different attachments to allow video recording the egg-laying animals and to deliver light for optogenetics studies. This article provides the blueprints for fabricating these chambers and the procedure for preparing the flies to be assayed in these chambers.

High Throughput Assay to Examine Egg-Laying Preferences of Individual Drosophila melanogaster

This protocol describes a high throughput assay for testing egg-laying preferences of Drosophila melanogaster at single-animal resolution. This assay provides a simple, efficient, and scalable platform to identify genes and circuit components that control a simple decision-making process.

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Taste Preference Assay for Adult Drosophila

Olfactory and gustatory perception of the environment is vital for animal survival. The most obvious application of these chemosenses is to be able to distinguish good food sources from potentially dangerous food sources. Gustation requires physical contact with a chemical compound which is able to signal through taste receptors that are expressed on the surface of neurons. In insects, these gustatory neurons can be located across the animal's body allowing taste to play an important role in many different behaviors. Insects typically prefer compounds containing sugars, while compounds that are considered bitter tasting are avoided. Given the basic biological importance of taste, there is intense interest in understanding the molecular mechanisms underlying this sensory modality. We describe an adult Drosophila taste assay which reflects the preference of the animals for a given tastant compound. This assay may be applied to animals of any genetic background to examine the taste preference for a desired soluble compound.

Taste Preference Assay for Adult Drosophila

Taste is an important sensory process which facilitates attraction to beneficial substances and avoidance of toxic substances. This protocol describes a simple ingestion assay for determining Drosophila gustatory preference for a given chemical compound.

Olfactory and gustatory perception of the environment is vital for animal survival.  The most obvious application of these chemosenses is to be able to ...

A Simple Way to Measure Alterations in Reward-seeking Behavior Using Drosophila melanogaster

We describe a protocol for measuring ethanol self-administration in fruit flies (Drosophila melanogaster) as a proxy for changes in reward states. We demonstrate a simple way to tap into the fly reward system, modify experiences related to natural reward, and use voluntary ethanol consumption as a measure for changes in reward states. The approach serves as a relevant tool to study the neurons and genes that play a role in experience-mediated changes of internal state. The protocol is composed of two discrete parts: exposing the flies to rewarding and nonrewarding experiences, and assaying voluntary ethanol consumption as a measure of the motivation to obtain a drug reward. The two parts can be used independently to induce the modulation of experience as an initial step for further downstream assays or as an independent two-choice feeding assay, respectively. The protocol does not require a complicated setup and can therefore be applied in any laboratory with basic fly culture tools.

A Simple Way to Measure Alterations in Reward-seeking Behavior Using Drosophila melanogaster

We describe a protocol for inducing rewarding and nonrewarding experiences in fruit flies (Drosophila melanogaster) using voluntary ethanol consumption as a measure for changes in reward states.

We describe a protocol for measuring ethanol self-administration in fruit flies (Drosophila melanogaster) as a proxy for changes in reward states. We ...

The CApillary FEeder Assay Measures Food Intake in Drosophila melanogaster

For most animals, feeding is an essential behavior for securing survival, and it influences development, locomotion, health and reproduction. Ingestion of the right type and quantity of food therefore has a major influence on quality of life. Research on feeding behavior focuses on the underlying processes that ensure actual feeding and unravels the role of factors regulating internal energy homeostasis and the neuronal bases of decision-making. The model organism Drosophila melanogaster, with its great variety of genetically traceable tools for labeling and manipulating single neurons, allows mapping of neuronal networks and identification of molecular signaling cascades involved in the regulation of food intake. This report demonstrates the CApillary FEeder assay (CAFE) and shows how to measure food intake in a group of flies for time spans ranging from hours to days. This easy-to-use assay consists of glass capillaries filled with liquid food that flies can freely access and feed on. Food consumption in the assay is accurately determined using simple measurement tools. Herein we describe step-by-step the method from setup to successful execution of the CAFE assay, and provide practical examples to analyze the food intake of a group of flies under controlled conditions. The reader is guided through possible limitations of the assay, and advantages and disadvantages of the method compared to other feeding assays in D. melanogaster are evaluated.

The CApillary FEeder Assay Measures Food Intake in Drosophila melanogaster

The CApillary FEeder (CAFE) assay is a simple, budget-friendly, highly reliable method for investigating mechanisms underlying food intake. Used with the highly versatile genetic model organism Drosophila melanogaster, it provides a powerful means of gaining new insights into regulatory mechanisms of food intake.

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Quantification of Macronutrients Intake in a Thermogenetic Neuronal Screen using Drosophila Larvae

Foraging and feeding behaviors allow animals to access sources of energy and nutrients essential for their development, health, and fitness. Investigating the neuronal regulation of these behaviors is essential for the understanding of the physiological and molecular mechanisms underlying nutritional homeostasis. The use of genetically tractable animal models such as worms, flies, and fish greatly facilitates these types of studies. In the last decade, the fruit fly Drosophila melanogaster has been used as a powerful animal model by neurobiologists investigating the neuronal control of feeding and foraging behaviors. While undoubtedly valuable, most studies examine adult flies. Here, we describe a protocol that takes advantage of the simpler larval nervous system to investigate neuronal substrates controlling feeding behaviors when larvae are exposed to diets differing in their protein and carbohydrates content. Our methods are based on a quantitative colorimetric no-choice feeding assay, performed in the context of a neuronal thermogenetic-activation screen. As a read-out, the amount of food eaten by larvae over a 1 h interval was used when exposed to one of the three dye-labeled diets that differ in their protein to carbohydrates (P:C) ratios. The efficacy of this protocol is demonstrated in the context of a neurogenetic screen in larval Drosophila, by identifying candidate neuronal populations regulating the amount of food eaten in diets of different macronutrient quality. We were also able to classify and group the genotypes tested into phenotypic classes. Besides a brief review of the currently available methods in the literature, the advantages and limitations of these methods are discussed and, also, some suggestions are provided about how this protocol might be adapted to other specific experiments.

Quantification of Macronutrients Intake in a Thermogenetic Neuronal Screen using Drosophila Larvae

Described here is a protocol that enables the colorimetric quantification of the amount of food eaten within a defined interval of time by Drosophila melanogaster larvae exposed to diets of different macronutrient quality. These assays are conducted in the context of a neuronal thermogenetic screen.

Foraging and feeding behaviors allow animals to access sources of energy and nutrients essential for their development, health, and fitness. Investigating ...

A Rapid Food-Preference Assay in Drosophila

To select food with nutritional value while avoiding the consumption of harmful agents, animals need a sophisticated and robust taste system to evaluate their food environment. The fruit fly, Drosophila melanogaster, is a genetically tractable model organism that is widely used to decipher the molecular, cellular, and neural underpinnings of food preference. To analyze fly food preference, a robust feeding method is needed. Described here is a two-choice feeding assay, which is rigorous, cost-saving, and fast. The assay is Petri-dish-based and involves the addition of two different foods supplemented with blue or red dye to the two halves of the dish. Then, ~70 prestarved, 2-4-day-old flies are placed in the dish and&#160;allowed to choose between blue and red foods in the dark for about 90 min. Examination of the abdomen of each fly is followed by the calculation of the preference index. In contrast to multiwell plates, each Petri dish takes only ~20 s to fill and saves time and effort. This feeding assay can be employed to quickly determine whether flies like or dislike a particular food.

A Rapid Food-Preference Assay in Drosophila

We present a protocol for a two-choice feeding assay for flies. This feeding assay is fast and easy to run and is suitable not only for small-scale laboratory research, but also for high-throughput behavioral screens in flies.

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Fast Colony Forming Unit Counting in 96-Well Plate Format Applied to the Drosophila Microbiome

The intestines of animals are colonized by commensal microbes, which impact host development, health, and behavior. Precise quantification of colonization is essential for studying the complex interactions between host and microbe both to validate the microbial composition and study its effects. Drosophila melanogaster,&#160;which has a low native microbial diversity and is economical to rear with defined microbial composition, has emerged as a model organism for studying the gut microbiome. Analyzing the microbiome of an individual organism requires identification of which microbial species are present and quantification of their absolute abundance. This article presents a method for the analysis of a large number of individual fly microbiomes. The flies are prepared in 96-well plates, enabling the handling of a large number of samples at once. Microbial abundance is quantified by plating up to 96 whole fly homogenates on a single agar plate in an array of spots and then counting the colony forming units (CFUs) that grow in each spot. This plating system is paired with an automated CFU quantification platform, which incorporates photography of the plates, differentiation of fluorescent colonies, and automated counting of the colonies using an ImageJ plugin. Advantages are that (i) this method is sensitive enough to detect differences between treatments, (ii) the spot plating method is as accurate as traditional plating methods, and (iii) the automated counting process is accurate and faster than manual counting. The workflow presented here enables high-throughput quantification of CFUs in a large number of replicates and can be applied to other microbiology study systems including in vitro and other small animal models.

Fast Colony Forming Unit Counting in 96-Well Plate Format Applied to the Drosophila Microbiome

This method quantifies microbial abundance using a 96-well plate format to plate colony forming units (CFUs) and is applied to the Drosophila microbiome in whole fly homogenate samples. CFUs are counted with an automated image analysis software provided here.

The intestines of animals are colonized by commensal microbes, which impact host development, health, and behavior. Precise quantification of colonization ...

A High Throughput Microplate Feeder Assay for Quantification of Consumption in Drosophila

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