Oxygen Consumption Measurements in Caenorhabditis elegans Using the Seahorse XF24

Materials and Reagents

1. 1,000 μl pipette tips (Neptune, catalog number: 89425-640)
2. 200 μl pipette tips (Neptune, catalog number: 89140-900)
3. 10 μl pipette tips (Neptune, catalog number: 89140-900)
4. 1.5 ml microcentrifuge tubes (VWR, catalog number: 20170-650)
5. 60 mm Petri dish (Santa Cruz Biotechnology, catalog number: 351863)
6. 25 ml serological pipet (VWR, catalog number: 89130-900)
7. 0.22 μm filter (Corning, catalog number: 430767)
8. Caenorhabditis elegans (N2, wildtype from CGC)
9. Triton X-100 (Fisher Scientific, catalog number: AC327371000)
10. NaCl (Fisher Scientific, catalog number: BP358-1)
11. Yeast Extract (BD, catalog number: 212750)
12. Tryptone (BD, catalog number: 211705)
13. Peptone (BD, catalog number: 211677)
14. Agar (BD, catalog number: 214530)
15. Ethyl Alcohol 200 proof (Greenfield Global, catalog number: 111000200)
16. Cholesterol (5 mg/ml in 200 proof ethyl alcohol) (Sigma-Aldrich, catalog number: C8667-1G) 
17. CaCl₂ (1 M, filter sterile) (VWR, catalog number: 97062-590)
18. MgSO₄ (1 M, filter sterile) (VWR, catalog number: IC191422.5)
19. KH₂PO₄ (1 M, filter sterile) (VWR, catalog number: 71003-456)
20. K₂HPO₄ (1 M, filter sterile) (VWR, catalog number: 470009-788)
21. Na₂HPO₄ (VWR, catalog number: 470302-662)
22. Dimethyl Sulfoxide (DMSO) (VWR, catalog number: 97061-250) 
23. Carbonyl cyanide-p-trifluoromethoxyphenylhydrazone (FCCP) (192 μM in DMSO) (Sigma-Aldrich, catalog number: C2920-10MG)
24. Potassium phosphate buffer (see Recipes)
25. M9 Buffer (see Recipes)
    
26. LB Broth for OP50 bacteria (see Recipes)
27. NGM plates (see Recipes)
    

Equipment

1. 1 ml pipetman (Eppendorf, catalog number: 3123000063)
2. 200 μl pipetman (Eppendorf, catalog number: 3124000083)
3. 20 μl pipetman (Eppendorf, catalog number: 3124000032)
4. Seahorse Extracellular Flux Analyzer (XFe24 Analyzer) (Agilent)
5. Seahorse XF24 FluxPak (Agilent, catalog number: 100850-001)
   Note: It contains 18 XF24 sensor cartridges, 20 XF24 cell culture microplates, and 1 bottle of Seahorse XF Calibrant Solution 500 ml.
6. 20 °C Incubator (VWR, catalog number: 10753-894) 
7. Pipette Controller (Brandtech Scientific Inc., catalog number: 26333)
   

Software

1. Seahorse XF24 Analyzer Software (Agilent)
2. Microsoft Excel or any other spreadsheet program required for post-experimental analysis.
   

Procedure

Note: To measure oxygen consumption, we adapted a published protocol (Dancy et al., 2016).

Grow worms at 20 °C on NGM plates spotted with OP50. Pick 300 L4-staged worms per condition to synchronize the experimental animals and age them as desired. The experimental animals should be at least in their second generation of being grown in an uncrowded, unstarved and uncontaminated environment.

1. Prior to the day of the experiment
   
   1. Calibrate the sensor cartridges
      The sensor cartridge has three parts: the lid, the cartridge itself containing probes on the bottom and ports for adding drugs on top, and the 24-well plate where the cartridge is placed in. Add 1 ml of calibrant solution into each well of the 24-well plate and incubate the plate at 37 °C overnight. 
   2. Make sure the heater on the Seahorse XF24 is turned off. Ideally, the temperature of the room where the experiment will be performed in should ideally not exceed 20 °C, and certainly not higher than 23 °C, to prevent the worms from receiving a heat-shock.
      
      
      
2. On the day of the experiment
   
   1. If assessing basal respiration only, start with Step B2. To assess maximal respiration, use the mitochondrial oxidative phosphorylation uncoupler FCCP, no other drugs are necessary. Pipet 75 μl of 192 μM FCCP into one of the 4 ports available for each well (Figure 2). For simultaneous release of FCCP into each well, distribute FCCP into the same port for each well (Figure 2). While wild-type worms will respond to this dose of FCCP, some optimization may be required for mutant strains.
      
      
      Figure 2. Schematic of the probe plate. The (A) side-view and (B) top-view of the 24-well sensor cartridge, where the sensor is in the center and the injection ports for compounds are in the periphery of each well. Pick the same injection port, which would be the ports of the same color, for each well when adding a compound.
      
      
   2. Make sure the equipment is at room temperature and the heater is turned off (Figure 3).
      
      
      Figure 3. Instructions to turn off the heater in the Seahorse X24. A. This screen appears once the program opens. Select the “Standard” mode (red circle), which opens the screen in (B). B. Select “Instrument” (red circle), which opens the screen in (C). C. Select “Administration” (red circle), which opens the screen in (D). D. Select “Temp. Control” (red circle), which opens the screen in (E). In this final screen, the circle next to “ON” should be clicked until it appears dim, similar to the figure, and then select “ok” on that screen.
      
      
   3. Run the calibration program with the cartridge.
   4. Prepare the XF24 cell culture microplates by adding 450 μl of M9 into each well. 
   5. Prepare worms:
      Worms tend to stick to plastics, so it is always necessary to wash the plastic pipet tips and centrifuge tubes with 0.1% Triton X-100 in M9 prior to aspirating and ejecting worms.
      
      1. Pre-wash centrifuge tube by adding 1 ml 0.1% Triton X-100 in M9. Remove the solution and replace it with 1 ml M9 using 1000 μl plastic pipette tips. 
      2. Pick 300 worms into a microcentrifuge tube.
      3. Gently pipet the worms to dissolve bacterial clumps that were transferred with the worms.
      4. Let the worms settle by gravity to the bottom of the 1.5 ml microcentrifuge tube and remove as much of the M9 buffer and bacteria as possible. 
      5. Add 1 ml M9 buffer and repeat Steps B5c and B5d twice. Keep the supernatant of the last wash which will be used as control for Step B5i. 
      6. Add 600 μl of M9 buffer to the worms.
      7. Cut off the end of a 200 μl tip to create a wide bore tip. Rinse it in 0.1% Triton M9 buffer by pipetting up and down in the solution. 
      8. Flick the tube gently to mix worms. Pipet 50 μl into a well of the XF24 cell culture microplates. Remember to flick the worms every time prior to pipetting them into the well. Each sample should be divided into 5 wells containing approximately 50 worms each.
      9. Arranging the samples in the XF24-well plate.
         
         1. Leave the four wells, A1, B4, C3, and D6, empty to be used as controls (Figure 4).
         2. Distribute each sample in random parts of the plate (Figure 4).
            
            
            Figure 4. A sample XF24 well plate with empty control wells A1, B4, C3 and D6. This mock plate contains 4 different conditions [C1 (orange), C2 (green), C3 (yellow), and C4 (orange)] with 5 replicates each (R1, R2, R3, R4, R5).
         
         
      10. Take an image of each well with worms to register the exact number of worms in each well at 20x magnification. Ideally, there should be between 50 and 70 worms. Less than 50 worms may result in greater variability and more than 70 worms in a well may result in an inaccurate assessment of the number of worms per well. 
      11. Leave the worms at 20 °C for one hour.
   6. Set up the program on the XF24 Analyzer as follows (Figure 5):
      
      1. Ten cycles of 2 min mixing, 2 min resting, 2 min reading. 
      2. When assessing maximal capacity, add a step to inject the ports and add 10 cycles of 2 min mixing, 2 min resting, 2 min reading.
      
      
      Figure 5. Seahorse XF24 protocol for acquiring maximal respiratory capacity. Note that when assessing basal respiration only, steps 8-13 should be removed. 

Data analysis

In order to analyze the data from the XF24 Analyzer Software, export the results into Microsoft Excel format and perform the following steps below in Microsoft Excel:

1. Normalize oxygen consumption values per well that is generated by the software to the number of worms for each time-point per well. 
2. To obtain the basal respiration rate: 
   
   1. For each well, average the oxygen consumption rate per well per worm (as calculated in step 1 of Data Analysis) for cycles 3 or 4 to 10.
      Note: The first two to three readings may be skipped because as worms adjust to their new environment, the initial readings may be noisy.
   2. Average the basal respiration rate of all 5 wells per condition.
   3. The data can be represented as bar graphs with the mean ± SEM when at least three technical replicates are included. Unpaired t-test can be performed to determine significance. 
3. To obtain the maximal respiration capacity:
   
   1. For each well, average the oxygen consumption rate for cycles 3 or 4 to 10. 
   2. Then for each well, identify the peak response in the ten readings after addition of FCCP. 
   3. Average the oxygen consumption rate of the peak reading and the two readings before and after it. 
   4. Divide the average oxygen consumption rate obtained in the previous step with the oxygen consumption rate obtained in step (a). 
   5. Average the maximal respiration capacity of all 5 wells per condition. The data can be represented as bar graphs with the mean ± SEM when at least three technical replicates are done. Unpaired t-test can be performed to determine significance. 
4. Control to measure the effects of the residual bacteria on oxygen consumption rates.
   
   1. Effects of the bacteria on oxygen consumption rates determined by the XF24 Analyzer software.
      
      1. The second wash from the preparation of worms in step B5e was collected and run on wells to compare to the respiration of the animals that were washed.
      2. Figure 6 shows that the basal rate of oxygen consumption in the wells with the residual bacteria in the second wash is less than 0.003% of the oxygen consumption of individual worms in the wells. The figure shows the oxygen consumption rate of the worms and the residual bacteria in the second wash on a logarithmic scale in order to make the values visible.
         
         
         Figure 6. Residual bacteria in the preparation of worms have minor impact on respiration measurements. A. A logarithmic scale was used to visualize the oxygen consumption rate per worm (OCR) in the wells containing worms (green) and the wells containing residual bacteria (orange). The average of ten readings per well and the standard deviation is represented. The last columns indicate the average of the data from the three wells containing 30, 45 and 87 worms. B. Image of the wells containing the worms that were assayed in (A).
         
         
         
   2. Effects of varying number of animals per well:
      
      1. Varying number of animals were placed in the wells and the basal oxygen consumption rate was determined. 
      2. Figure 7 shows that there is a strong correlation between the oxygen consumption rate and the number of animals per well.
         
         
         Figure 7. The basal respiration is linearly related to the number of 5-day old wildtype worms per well

Recipes

1. Potassium phosphate buffer
   Add enough 1 M K₂HPO₄ to 400 ml of 1 M KH₂PO₄ to obtain a pH 6.0 solution
   Note: The amount of 1 M K₂HPO₄ may vary each time the solution is made.
2. M9 Buffer
   
   1. Add 3 g KH₂PO₄, 6 g Na₂HPO₄, 5 g NaCl, 1 ml 1 M MgSO₄ and bring up the solution to 1 L with distilled water
   2. Filter sterilize the solution using 0.22 μm filter (Corning)
3. LB Broth for OP50 bacteria (OP50 from CGC)
   
   1. Add 10 g NaCl, 5 g Yeast Extract, 10 g Tryptone to 1 L of distilled water
   2. Sterilize by autoclaving for 20 min
   3. Do not use any antibiotics
4. NGM plates
   
   1. Add 3 g of NaCl, 2.5 g peptone, 17 g of agar to 1 L of distilled water
   2. Sterilize by autoclaving for 20 min
   3. Cool the media to 55 °C
   4. Add 1 ml of 5 mg/ml cholesterol, 1 ml of 1 M CaCl₂, 1 ml of 1 M MgSO₄, and 25 ml of phosphate potassium buffer 
   5. Mix and pour 10 ml into 60 mm dishes
   6. Start overnight cultures of OP50 in LB broth shaking at 200 rpm in a 37 °C incubator with NO antibiotics
   7. The next day, spot 4-5 drops of the overnight cultures of OP50 using a 25 ml serological pipet

Acknowledgments

This work was supported by grants from the NIH (R01-GM124532 to M.V.; CA204894 and ES026222 to J.H.B.), a grant from NIEHS (T32-ES019851 to C.F.), and a pilot award from UPenn (FP20457 to M.V.).

Competing interests

The contents of this publication do not necessarily represent the official views of the NIH.

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