Materials and Reagents

Petri dish 60 x 15 mm (SARSTEDT, catalog number: 82.1194.500 )
15 ml conical tube
Frosted microscope slides (size: 1 x 3” ; thickness: 1-2 mm) (UltiDent Scientific, catalog number: 170-7107A )
Microscope cover glass (size: 22 x 22 #1.5) (Fisher Scientific, catalog number: 12-541B )
Platinum wire (Thomas Scientific, catalog number: 1233S71 )
Pasteur pipet (Fisher Scientific, catalog number: 13-678-20C )
E. coli bacteria HT115^DE3 with the plasmid pL4440-empty vector
E. coli bacteria HT115^DE3 with the plasmid pL4440-oct-1 (Ahringer’s collection). Sequence verified
E. coli bacteria HT115^DE3with the plasmid pL4440-oct-2 (Ahringer’s collection). Sequence verified
Bristol N2 (wild type) and RB1084 [oct-1(ok1051) I] from Caenorhabditis Genetic Center
Ampicillin (Sigma-Aldrich, catalog number: A9518 )
Potassium phosphate monobasic (KH₂PO₄) (Bio Basic, catalog number: PB0445 )
Magnesium sulfate (MgSO₄) (Bio Basic, catalog number: MRB0329 )
Calcium chloride dihydrate (CaCl₂) (Fisher Scientific, catalog number: C79-500 )
Cholesterol (Sigma-Aldrich, catalog number: C8503 )
Ethanol 100% (works from any company)
Doxorubicin (for Research from Hôpital Maisonneuve-Rosemont, Montreal, Canada). Stock concentration at 2 mg/ml
IPTG (Bio Basic, catalog number: PRB0447 )
Levamisol hydrochloride (MP Biomedical, catalog number: 155228 )
Clear nail polish from Wild Shine from Dollarama
Tryptone (Bio Basic, catalog number: TG217 (G211)) for Luria Broth (LB) media
Yeast extract (Wisent Bioproducts, catalog number: 800-150-LG ) for LB media
Sodium chloride (NaCl) (Wisent Bioproducts, catalog number: 600-082 )
Bacteriological agar (Wisent Bioproducts, catalog number: 800-010-CG )
Peptone (Wisent Bioproducts, catalog number: 800-157-LG ) for nematode grown media (NGM)
Agarose (Wisent Bioproducts, catalog number: 800-015-CG )
Sodium hydroxide (NaOH) (Bio Basic, catalog number: SB0617 )
Bleach Lavo Pro6 (Lavo Inc, Montreal, Canada)
Sodium phosphate dibasic (Na₂HPO₄) (Bio Basic, catalog number: S0404 )
LB solution (see Recipes)
Nematode growth media (NGM) (see Recipes)
Agar pad (see Recipes)
Alkaline Hypochlorite solution for bleaching the worms (see Recipes)
M9 buffer (see Recipes)

Equipment

Incubator at 20 °C, but with a range from 15 to 37 °C (SHEL LAB, model: 2020 )
37 °C incubator (Panasonic Healthcare, model: Mir-262 )
37 °C shaker (Inforst, model: Multitron Standard )
500 ml glass bottle (Wheaton graduated glass media bottles with lined caps)
Microwave (inverter model, Panasonic Healthcare)
55 °C water bath (Precision Scientific, catalog number: 66800 )
Metal spatula (VWR)
Flame
Neutrex culture tubes 16 x 15 mm
Pyrex Erlenmeyer flask different sizes for bacteria culturing
Autoclave
Stereomicroscope Leica MZ 8 (Leica 10445538 Plan Microscope Objective Lens 1.0x) (Leica, model: MZ 8 )
DeltaVision Elite Restoration System (GE Healthcare, model: DeltaVision Elite High Resolution Microscope ) and the DeltaVision imaging system user’s manual
Fisher Vortex Genie 2 (Fisher Scientific, catalog number: 12-812 )
Eppendorf 5810 R centrifuge (Eppendorf, model: 5810 R )
VWR rocking platform shakers basic (VWR)
Ptc-100 Programmable Thermal Controller 96 Well (Bio-Rad Laboratories, model: Ptc-100^® Programmable Thermal Controller )
Centrifuge (Sigma Centrifuge, model: Sigma 1-14 )

Software

ImageJ imaging software
SoftWorx software

Procedure

Preparation of bacteria and media for worm growth
1. Bacteria preparation (C. elegans food)
2. C. elegans growth media preparation
  1. Melt the solid NGM contained in a glass bottle (500 ml) using a microwave (power level 2 for 25 min).
  2. Keep the melted medium at 55 °C in a water bath for 15-20 min.
  3. Before usage, add:
    12.5 ml of 1 M KH₂PO₄ pH 6
    500 µl of 1 M MgSO₄
    500 µl of 1 M CaCl₂
    500 µl cholesterol (stock 5 mg/ml in 95% ethanol)
    500 µl of ampicillin (stock 100 mg/ml), if using knockdown bacteria strain HT115^DE3 carrying the L4440 vector or the target gene.
  4. Gently invert the bottle a few times to mix all the ingredients and then pour 6 ml of the medium into each of 60 x 15 mm Petri dish.
  5. Let it dry at room temperature for around 1 h.
  6. Once dried, using a sterilized bacterial plating rod spread 70 µl of bacteria prepared in step A1 above to form a lawn. The optical density OD₆₀₀ of the bacteria is approximately 1.0. Alternatively, the bacteria can be added as 3 drops distributed onto the plate.
  7. Incubate the plate overnight at 37 °C.
3. Worm growth
Worm synchronisation
1. The 4 plates are expected to be filled with adult worms, visualized through a stereomicroscope, and at which point the synchronization can be done. An alternative method to obtain a huge amount of worms is to grow them in liquid media (NGM medium without agar).
2. Add 2 ml of alkaline hypochlorite solution (bleaching solution) to each plate and rapidly collect the worms by pipetting (about 10 sec per plate) in a sterile 15 ml conical tube. Date and label the tube with the name of the worm strain. Alternatively, harvest the worms with 1 ml of M9 buffer and collect them into 15 ml conical tubes. Centrifuge in the Eppendorf 5810 R centrifuge, using swing bucket rotor (A-4-81) with adapters for 15 ml conical tubes at 1,740 x g for 2 min at 4 °C. Discard the M9 buffer and add 2 ml of the bleaching solution. In this way the worms are washed once.
3. Quickly start to vortex the worms for 7 min at setting 8 on the vortex and check under the stereomicroscope if the adult worms are lysed and only the eggs are present.
  Note: Steps B2 and B3 must be carried out with care as they are critical for the eggs to hatch.
4. Without any delay, centrifuge in the Eppendorf 5810 R centrifuge at 1,740 x g for 2 min at 4 °C.
5. Aspirate the supernatant, but leave approximately 1 ml of the solution.
6. Adding 5 ml of M9 buffer and repeat the centrifugation and aspiration as in steps B4 and B5.
7. Repeat 4 more times step B6, in order to remove any trace of the bleaching solution.
8. Incubate the eggs in the final 1 ml of M9 buffer overnight at 20 °C. During this time the eggs will hatch and produce L1 stage worms.
Worm under treatment
1. Bacteria preparation
  1. In 3 different tubes, add 10 ml LB medium and 10 µl ampicillin (100 mg/ml).
  2. In the 1^st tube, add a few colonies of E. coli HT115^DE3/empty vector L4440.
  3. In the 2^nd tube, add a few colonies of E. coli HT115^DE3/pL4440-oct-1.
  4. In the 3^rd tube, add a few colonies of E. coli HT115^DE3/pL4440-oct-2.
  5. Incubate all the tubes for 5 h in a 37 °C orbital shaker.
2. Drug plate preparation
  1. Melt a bottle of 500 ml of solid NGM as above (see C. elegans growth media preparation above).
  2. For normal drug plates-no knockdown
    1. Transfer 30 ml of melted NGM media kept at 55 °C into a small sterile bottle. This will make 3 Petri dishes (60 x 15 mm) each containing ~10 ml of NGM media for triplicate assays.
    2. Add the doxorubicin (stock 2 mg/ml) to the desired final concentrations for each 6 ml of NGM media and pour onto the 60 x 15 mm Petri dish. For doxorubicin use between 0.1 to 100 µM depending on the strains. Uptake was observed with as low as 0.5 µM of doxorubicin.
      IMPORTANT: Do not forget to prepare a plate without drug.
    3. Leave plates for at least 15 min at room temperature for the medium to solidify.
    4. Add 70 µl E. coli HT115^DE3/pL4440-empty vector bacteria.
    5. Incubate the plates overnight at 37 °C.
  3. For knockdown drug plates
3. Now all the plates are ready to add 50 µl of the L1 synchronized worms.
4. Verify if there are nearly 50 L1-staged worms on the plates under the stereomicroscope.
5. Incubate the plates at 20 °C for 3 days.
Microscope visualisation
1. Preparation of slides
  1. On a frosted microscope slide add one drop (~50 µl) of 3% agarose and squeeze it with another slide to form a sandwich. After 10 sec, remove one of the slide to expose the agarose.
  2. Dry the slide with the agarose at 65 °C around 15-30 min using a Programmable Thermal Controller 96 Well.
2. Mounting the worms
  1. Add 7 µl of 1 M levamisol onto the surface of the dried agar on the slide.
  2. To each slide, add 10-15 young adult worms from a single treatment condition by using a platinum wire to transfer the worms.
  3. Sterilize the platinum wire using a flame before transferring the next 10-15 worms from a different treatment condition onto a new slide.
  4. Add the coverslip and seal around the slide and coverslip with clear nail polish.
3. Microscopy visualisation
  The slide containing the worm is ready to be visualised. Place the slide on the stage of an epifluorescence microscope.
  1^st Adjust the objectives
  2^nd Select the filters and adjust all the necessary parameters
  3^rd Once everything is ready, start capturing the images
  4^th Save the images
  Below is a detail description to visualize the worms using a DeltaVision microscope.
  1. Add a small drop of DeltaVision Immersion oil 1.534 onto the slide in order to use objective 40x.
  2. Place the mounted slide on the microscope by inverting it.
  3. Adjust the eyepiece filter roll to POL filter.
  4. Open the SoftWorx software . See GE Healthcare manual (GE Healthcare, 2014).
  5. Press on the microscope.
    3 windows will be opened (Figure 1).
    
    Figure 1. SoftWorx desktop display. The Resolve3D window includes acquisition parameters and controls for moving the stage, the Data Collection window displays images as they are acquired, and the Filter Monitor displays the filters currently selected.
  6. On the window called Resolve3D (Figure 1).
  7. Press on the gear wheel (setting) to open Resolve3D setting window (Figure 2).
    
    Figure 2. Resolve3D window setting
  8. In the Resolve3D window (Figure 1), set the following parameters in Figure 4.
    
    Figure 4. Setting the parameters
    1. Excitation: POL.
    2. Emission: POL.
    3. % T: 32%.
    4. Exposure: 0.025.
    5. Lens: 40x.
  9. Press on the Erlenmeyer.
  10. A window called Design/Run Experiment window will be opened (Figure 5).
    
    Figure 5. Design and Run experiment window
4. Result analysis

Data analysis

The result is representative of a single worm from an experiment where 10 worms were placed onto the slide (Figure 8). The experiment was repeated three times with identical data. Fluorescence posterior to the pharynx is autofluorescence detected from the intestine (Figure 8). The data were quantified using ImageJ according to Papaluca and Ramotar (2016).

Figure 8. Uptake of doxorubicin in the N2 wild type animals downregulated for oct-1 that causes upregulation of OCT-2. Previously, we showed that downregulation stimulated expression of oct-2, which drives uptake of drugs into C. elegans (Papaluca and Ramotar, 2016). A. Untreated; the absence of doxorubicin is illustrated by the lack of yellow fluorescence and the green background is autofluorescence from ingestion of food by the animal. B. Treated with doxorubicin (1 µM). Doxorubicin uptake is visible as yellow due to the merge of the green autofluorescence and red fluorescence from the drug. Circles show the location of the pharynx. Scale bars = 50 µm. See Data analysis for additional details.

Notes

Instead of using frozen bacteria as worm food, we typically use fresh culture of the bacteria.
Always work under sterile conditions. Be on the watch for fungus (white to black like spider net) and rarely mushroom (brownish spots). If this is the case, the best solution will be to bleach the worms and collect the eggs for new larvae.

Recipes

LB solution
5 g tryptone
2.5 g yeast extract
5 g NaCl
ddH₂O up to 500 ml
Add 7.5 g of agar, if making solid media plates
Nematode growth media (NGM)
1.25 g peptone
1.5 g NaCl
8.75 g agar
ddH₂O up to 500 ml
Autoclave
When the media is between 50 to 55 °C, add the following constituents before pouring the plates:
12.5 ml of 1 M KH₂PO₄ pH 6
500 µl of 1 M MgSO₄
500 µl of 1 M CaCl₂
500 µl cholesterol (stock 5 mg/ml in 95% ethanol)
500 µl of ampicillin (stock 100 mg/ml), if using the plasmid containing bacteria HT115^DE3
Agar pad
3% agarose in MilliQ water
Melt when needed
Alkaline hypochlorite solution (bleaching solution) (make fresh monthly)
8.25 ml ddH₂O
3.75 ml 1 N NaOH
3.00 ml Bleach (Javel)
M9 buffer (1 L)
6 g Na₂HPO₄
3 g KH₂PO₄
5 g NaCl
0.25 g MgSO₄·7H₂O
Sterilized by autoclaving

Acknowledgments

This work was funded by the research grant (RGPIN/202432-2012) to D.R. from the Natural Science and Engineering Research Council of Canada. A brief version of this protocol was previously described (Papaluca and Ramotar, 2016).

References

Burns, A. R., Wallace, I. M., Wildenhain, J., Tyers, M., Giaever, G., Bader, G. D., Nislow, C., Cutler, S. R. and Roy, P. J. (2010). A predictive model for drug bioaccumulation and bioactivity in Caenorhabditis elegans. Nat Chem Biol 6(7): 549-557.
Cesar-Razquin, A., Snijder, B., Frappier-Brinton, T., Isserlin, R., Gyimesi, G., Bai, X., Reithmeier, R. A., Hepworth, D., Hediger, M. A., Edwards, A. M. and Superti-Furga, G. (2015). A call for systematic research on solute carriers. Cell 162(3): 478-487.
Cheah, I. K., Ong, R. L., Gruber, J., Yew, T. S., Ng, L. F., Chen, C. B. and Halliwell, B. (2013). Knockout of a putative ergothioneine transporter in Caenorhabditis elegans decreases lifespan and increases susceptibility to oxidative damage. Free Radic Res 47(12): 1036-1045.
GE Healthcare (2014). DeltaVision Imaging System User’s Manual. PN 29087880 AB.
O’Reilly, L. P., Luke, C. J., Perlmutter, D. H., Silverman, G. A. and Pak, S. C. (2014). C. elegans in high-throughput drug discovery. Adv Drug Deliv Rev 69-70: 247-253.
Papaluca, A. and Ramotar, D. (2016). A novel approach using C. elegans DNA damage-induced apoptosis to characterize the dynamics of uptake transporters for therapeutic drug discoveries. Sci Rep 6: 36026.
Wu, X., Fei, Y. J., Huang, W., Chancy, C., Leibach, F. H. and Ganapathy, V. (1999). Identity of the F52F12.1 gene product in Caenorhabditis elegans as an organic cation transporter. Biochim Biophys Acta 1418(1): 239-244.