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://www.jove.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://www.jove.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://www.jove.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://www.jove.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://www.jove.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 border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>0.25 mm Diameter Needers</td>
			<td>Rave Scientific</td>
			<td>RS-MN-52-001012</td>
			<td></td>
		</tr>
		<tr>
			<td>0.45 &#181;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&#38;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>CO2 Anesthesia: The Flypads&#160; 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, 15396-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&#34; x 1/8&#34; 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://www.jove.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://www.jove.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://www.jove.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://www.jove.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://www.jove.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://www.jove.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://www.jove.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://www.jove.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 ...

a-high-throughput-microplate-feeder-assay-for-quantification

Research

JoVE Journal

Behavior

3.1K 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

Handwriting Analysis Indicates Spontaneous Dyskinesias in Neuroleptic Na&#239;ve Adolescents at High Risk for Psychosis

Growing evidence suggests that movement abnormalities are a core feature of psychosis. One marker of movement abnormality, dyskinesia, is a result of impaired neuromodulation of dopamine in fronto-striatal pathways. The traditional methods for identifying movement abnormalities include observer-based reports and force stability gauges. The drawbacks of these methods are long training times for raters, experimenter bias, large site differences in instrumental apparatus, and suboptimal reliability. Taking these drawbacks into account has guided the development of better&#160;standardized and more efficient procedures to examine movement abnormalities through handwriting analysis software and tablet. Individuals at&#160;risk for psychosis showed significantly more dysfluent pen movements (a proximal measure for dyskinesia) in a handwriting task. Handwriting kinematics offers a great advance over previous methods of assessing dyskinesia, which could clearly be beneficial for understanding the etiology of psychosis.

Handwriting Analysis Indicates Spontaneous Dyskinesias in Neuroleptic Na&amp;#239;ve Adolescents at High Risk for Psychosis

Handwriting analysis software significantly improves upon existing instruments measuring movement disorders. Individuals at&#160;risk for psychosis and healthy controls completed handwriting tasks to test for dyskinesia. Results suggest that youth at&#160;risk for psychosis exhibit dyskinesia and that handwriting analysis could significantly contribute to wider dissemination of early identification efforts

Growing evidence suggests that movement abnormalities are a core feature of psychosis. One marker of movement abnormality, dyskinesia, is a result of ...

Measurement of Fronto-limbic Activity Using an Emotional Oddball Task in Children with Familial High Risk for Schizophrenia

Adolescence is a critical developmental period where the early symptoms of schizophrenia frequently emerge. First-degree relatives of people with schizophrenia who are at familial high risk (FHR) may show similar cognitive and emotional changes. However, the neurological changes underlying the emergence of these symptoms remain unclear. This study sought to identify differences in frontal, striatal, and limbic regions in children and adolescents with FHR using functional magnetic resonance imaging. Groups of 21 children and adolescents at FHR and 21 healthy controls completed an emotional oddball task that relied on selective attention and the suppression of task-irrelevant emotional information. The standard oddball task was modified to include aversive and neutral distractors in order to examine potential group differences in both emotional and executive processing. This task was designed specifically to allow for children and adolescents to complete by keeping the difficulty and emotional image content age-appropriate. Furthermore, we demonstrate a technique for suitable fMRI registration for children and adolescent participants. This paradigm may also be applied in future studies to measure changes in neural activity in other populations with hypothesized developmental changes in executive and emotional processing.

This paper describes how to use the emotional oddball task and fMRI to measure brain activation in children and adolescents at familial high risk for schizophrenia (FHR).&#160;FMRI was used to measure differences in fronto-striato-limbic regions during an emotional oddball task. Children with FHR exhibited abnormal functional activation during adolescence.

Adolescence is a critical developmental period where the early symptoms of schizophrenia frequently emerge. First-degree relatives of people with ...

Moderate Prenatal Alcohol Exposure and Quantification of Social Behavior in Adult Rats

Alterations in social behavior are among the major negative consequences observed in children with Fetal Alcohol Spectrum Disorders (FASDs). Several independent laboratories have demonstrated robust alterations in the social behavior of rodents exposed to alcohol during brain development across a wide range of exposure durations, timing, doses, and ages at the time of behavioral quantification. Prior work from this laboratory has identified reliable alterations in specific forms of social interaction following moderate prenatal alcohol exposure (PAE) in the rat that persist well into adulthood, including increased wrestling and decreased investigation. These behavioral alterations have been useful in identifying neural circuits altered by moderate PAE1, and may hold importance for progressing toward a more complete understanding of the neural bases of PAE-related alterations in social behavior. This paper describes procedures for performing moderate PAE in which rat dams voluntarily consume ethanol or saccharin (control) throughout gestation, and measurement of social behaviors in adult offspring.

The goal of the protocol presented here is to describe procedures to expose rats to moderate levels of alcohol during prenatal brain development and to quantify resulting alterations in social behavior during adulthood.

Alterations in social behavior are among the major negative consequences observed in children with Fetal Alcohol Spectrum Disorders (FASDs). Several ...

The Treadmill Fatigue Test: A Simple, High-throughput Assay of Fatigue-like Behavior for the Mouse

Fatigue is a prominent symptom in many diseases and disorders and reduces quality of life for many people. The lack of clear pathogenesis and failure of current interventions to adequately treat fatigue in all patients leaves a need for new treatment options. Despite the therapeutic need and importance of preclinical research in helping identify promising novel treatments, few preclinical assays of fatigue are available. Moreover, the most common preclinical assay used to assess fatigue-like behavior, voluntary wheel running, is not suitable for use with some strains of mice, may not be sensitive to drugs that reduce fatigue, and has relatively low throughput. The current protocol describes a novel, non-voluntary preclinical assay of fatigue-like behavior, the treadmill fatigue test, and provides evidence of its efficacy in detecting fatigue-like behavior in mice treated with a chemotherapy drug known to cause fatigue in humans and fatigue-like behavior in animals. This assay may be a beneficial alternative to wheel running, as fatigue-like behavior and potential interventions can be assessed in a greater number of mice over a shorter time frame, thus permitting faster discovery of new therapeutic options.

Fatigue is a common, undertreated and frequently poorly-understood symptom in many diseases and disorders. New preclinical assays of fatigue may help to improve current understanding and future treatment of fatigue. To that end, the current protocol provides a novel means of measuring fatigue-like behavior in the mouse.

Fatigue is a prominent symptom in many diseases and disorders and reduces quality of life for many people. The lack of clear pathogenesis and failure of ...

A Method to Test the Effect of Environmental Cues on Mating Behavior in Drosophila melanogaster

An individual's sexual drive is influenced by genotype, experience and environmental conditions. How these factors interact to modulate sexual behaviors remains poorly understood. In Drosophila melanogaster, environmental cues, such as food availability, affect mating activity offering a tractable system to investigate the mechanisms modulating sexual behavior. In D. melanogaster, environmental cues are often sensed via the chemosensory gustatory and olfactory systems. Here, we present a method to test the effect of environmental chemical cues on mating behavior. The assay consists of a small mating arena containing food medium and a mating couple. The mating frequency for each couple is continuously monitored for 24 h. Here we present the applicability of this assay to test environmental compounds from an external source through a pressurized air system as well as manipulation of the environmental components directly in the mating arena. The use of a pressurized air system is especially useful to test the effect of very volatile compounds, while manipulating components directly in the mating arena can be of value to ascertain a compound's presence. This assay can be adapted to answer questions about the influence of genetic and environmental cues on mating behavior and fecundity as well as other male and female reproductive behaviors.

A Method to Test the Effect of Environmental Cues on Mating Behavior in Drosophila melanogaster

We demonstrate an assay to analyze the environmental and genetic cues that influence mating behavior in the fruit fly Drosophila melanogaster.

An individual's sexual drive is influenced by genotype, experience and environmental conditions. How these factors interact to modulate sexual behaviors ...

Application of MultiColor FlpOut Technique to Study High Resolution Single Cell Morphologies and Cell Interactions of Glia in Drosophila

Cells display different morphologies and complex anatomical relationships. How do cells interact with their neighbors? Do the interactions differ between cell types or even within a given type? What kinds of spatial rules do they follow? The answers to such fundamental questions in vivo have been hampered so far by a lack of tools for high resolution single cell labeling. Here, a detailed protocol to target single cells with a MultiColor FlpOut (MCFO) technique is provided. This method relies on three differently tagged reporters (HA, FLAG and V5) under UAS control that are kept silent by a transcriptional terminator flanked by two FRT sites (FRT-stop-FRT). A heat shock pulse induces the expression of a heat shock-induced Flp recombinase, which randomly removes the FRT-stop-FRT cassettes in individual cells: expression occurs only in cells that also express a GAL4 driver. This leads to an array of differently colored cells of a given cell type that allows the visualization of individual cell morphologies at high resolution. As an example, the MCFO technique can be combined with specific glial GAL4 drivers to visualize the morphologies of the different glial subtypes in the adult Drosophila brain.

Application of MultiColor FlpOut Technique to Study High Resolution Single Cell Morphologies and Cell Interactions of Glia in Drosophila

Cells display different morphologies and establish a variety of interactions with their neighbors. This protocol describes how to reveal the morphology of single cells and to investigate cell-cell interaction by using the well-established Gal4/UAS expression system.

Cells display different morphologies and complex anatomical relationships. How do cells interact with their neighbors? Do the interactions differ between ...

An Automated Rapid Iterative Negative Geotaxis Assay for Analyzing Adult Climbing Behavior in a Drosophila Model of Neurodegeneration

Neurodegenerative diseases are frequently associated with a progressive loss of movement ability, reduced life span, and age-dependent neurodegeneration. To understand the mechanism of these cellular events, and their causal relationships with each other, Drosophila melanogaster, with its sophisticated genetic tools and diverse behavioral features, are used as disease models for assessing neurodegenerative phenotypes. Here we describe a high-throughput method to analyze Drosophila adult negative geotaxis behavior, as an indication for possible motor defects associated with neurodegeneration. An automated machine is designed and developed to drive fly synchronization using an initial electric impulse, later allowing the recording of negative geotaxis behavior over a course of secs to mins. Images from the digitally recorded video are then processed with the self-designed RflyDetection software for statistical data manipulation. Different from the manually controlled negative geotaxis assay based on single fly, this precise, fast, and high-throughput protocol allows data acquisition from more than hundreds of flies simultaneously, providing an efficient approach to advance our understanding in the underlying mechanism of locomotor deficits associated with neurodegeneration.

An Automated Rapid Iterative Negative Geotaxis Assay for Analyzing Adult Climbing Behavior in a Drosophila Model of Neurodegeneration

This step-by-step protocol analyzes Drosophila negative geotaxis behavior using an automated multi-cylinder system that hosts hundreds of flies and synchronizes their action by an electric motor. Upon synchronization, fly negative geotaxis behavior is assayed, digitally recorded, and analyzed using the self-designed RflyDetection software.

Neurodegenerative diseases are frequently associated with a progressive loss of movement ability, reduced life span, and age-dependent neurodegeneration. ...

A Burrowing/Tunneling Assay for Detection of Hypoxia in Drosophila melanogaster Larvae

Oxygen deprivation in animals can result from exposure to low atmospheric oxygen levels or from internal tissue damage that interferes with oxygen distribution. It is also possible that aberrant behavior of oxygen-sensing neurons could induce hypoxia-like behavior in the presence of normal oxygen levels. In D. melanogaster, development at low oxygen levels results in inhibition of growth and sluggish behavior during the larval phases. However, these established manifestations of oxygen deficit overlap considerably with the phenotypes of many mutations that regulate growth, stress responses or locomotion. As result, there is currently no assay available to identify i) cellular hypoxia induced by a mutation or ii) hypoxia-like behavior when induced by abnormal neuronal behavior.
We have recently identified two distinctive behaviors in D. melanogaster larvae that occur at normal oxygen levels in response to internal detection of hypoxia. First, at all stages, such larvae avoid burrowing into food, often straying far away from a food source. Second, tunneling into a soft substratum, which normally occurs during the wandering third instar stage is completely abolished if larvae are hypoxic. The assay described here is designed to detect and quantitate these behaviors and thus to provide a way to detect hypoxia induced by internal damage rather than low external oxygen. Assay plates with an agar substratum and a central plug of yeast paste are used to support animals through larval life. The positions and state of the larvae are tracked daily as they proceed from first to third instar. The extent of tunneling into the agar substratum during wandering phase is quantitated after pupation using NIH ImageJ. The assay will be of value in determining when hypoxia is a component of a mutant phenotype and thus provide insight into possible sites of action of the gene in question.

A Burrowing/Tunneling Assay for Detection of Hypoxia in Drosophila melanogaster Larvae

The protocol describes a simple assay to identify Drosophila melanogaster larvae that are experiencing hypoxia under normal atmospheric oxygen levels. This protocol allows hypoxic larvae to be distinguished from other mutants that show overlapping phenotypes such as sluggishness or slow growth.

Oxygen deprivation in animals can result from exposure to low atmospheric oxygen levels or from internal tissue damage that interferes with oxygen ...

Noninvasive, High-throughput Determination of Sleep Duration in Rodents

Traditionally, sleep is monitored by an electroencephalogram (EEG). EEG studies in rodents require surgical implantation of the electrodes followed by a long recovery period. To perform an EEG recording, the animal is connected to a receiver, creating an unnatural tether to the head-mount. EEG monitoring is time consuming, carries risk to the animal, and is not a completely natural setting for the measurement of sleep. Alternative methods to detect sleep, particularly in a high-throughput fashion, would greatly advance the field of sleep research. Here, we describe a validated method for detecting sleep via activity-based home-cage monitoring. Previous studies have shown that sleep assessed via this method has a high degree of agreement with sleep defined by traditional EEG-based measures. Whereas this method is validated for total sleep time, it is important to note that sleep bout duration should be assessed by an EEG which has better temporal resolution. The EEG can also differentiate rapid eye movement (REM) and non-REM sleep, giving more detail about the exact nature of sleep. Nevertheless, activity-based sleep determination can be used to analyze multiple days of undisturbed sleep and to assess sleep as a response to an acute event (like stress). Here, we show the power of this system to detect the response of mice to daily intraperitoneal injections.

We describe a high-throughput method of measuring sleep by means of activity-based home-cage monitoring. This method offers advantages over traditional EEG-based methods. It is well validated for the determination of total sleep duration and can be a powerful tool to monitor sleep in rodent models of human disease.

Traditionally, sleep is monitored by an electroencephalogram (EEG). EEG studies in rodents require surgical implantation of the electrodes followed by a ...

High-Throughput Method for Measuring Alcohol Sedation Time of Individual Drosophila melanogaster

Drosophila melanogaster provides an excellent model to study the genetic underpinnings of alcohol sensitivity. In contrast to studies in human populations, the Drosophila model allows strict control over genetic background, and virtually unlimited numbers of individuals of the same genotype can be reared rapidly under well-controlled environmental conditions without regulatory restrictions and at relatively low cost. Flies exposed to ethanol undergo physiological and behavioral changes that resemble human alcohol intoxication, including loss of postural control, sedation, and development of tolerance. Here, we describe a simple, low-cost, high-throughput assay for assessing alcohol sedation sensitivity in large numbers of single flies. The assay is based on video recording of single flies introduced without anesthesia in 24-well cell culture plates in a set-up that enables synchronous initiation of alcohol exposure. The system enables a single person to collect individual ethanol sedation data on as many as 2,000 flies within an 8 h work period. The assay can, in principle, be extended to assess the effects of exposure to any volatile substance and applied to measure effects of acute toxicity of volatiles on other insects, including other fly species.

High-Throughput Method for Measuring Alcohol Sedation Time of Individual Drosophila melanogaster

Current methods to measure alcohol sensitivity in Drosophila are designed to test groups of flies. We present a simple, low-cost, high-throughput assay for assessing alcohol sedation sensitivity in large numbers of single flies. The method does not require specialized tools and can be performed in any laboratory using common materials.