Sample collection and eDNA extraction from Sterivex filter units

A portable peristaltic pump (Vampire sampler; Buerkle) is used for sampling at an approximate 30-50 mL/min flow rate. The tubing inserted in the unit's head has a suction hose (Marprene; 4.8 mm inner diameter), connected to a flexible silicone hose. A suitable adapter connects both hoses.

A Sterivex filter unit (0.22 µm pore size) is attached to the suction hose by a stainless steel male Luer-lock ring hose barb (1/4'). We recommend using a hose clip (9-10 mm; Buerkle cat. no. BURK8678-000) to firmly tight the Luer-lock ring to the hose. Each filter can process up to 2L of water depending on the amount of the suspended material.

Once the water sample is filtered, remove the remaining liquid from the Sterivex unit using a 5 mL sterilized syringe or similar by pushing air.

Cap both ends of the Sterivex. If the units have a male tip outlet, Parafilm can be used to cap them. Be aware of potential leakage, and make sure the Sterivex is dried and well sealed.

Now that the samples are ready and sealed, do not forget to identify them accordingly. A good rule of thumb is to write down ID, date, replicate number, filtered volume and station on the filter. Do the same on the sample bags, especially if there are more filters per site or replicate. The samples are store at -20°C degrees.

Place the Sterivex vertically (with the inlet cap upward) and load 900µLof ST1B buffer. ST1B is stored at 4°C. Be careful putting the pipette tip through the inlet (orange cap). Dispense the buffer slowly; a fraction of the volume can be lost.

Allow mixing in a vortex with a horizontal adapter (Qiagen, Cat. No. 13000-V1-5) for 00:05:00 at the minimum speed. Set the filters with the inlet facing out and check for potential leakage from the outlet sealed with Parafilm.

Rotate the Sterivex in 90 degrees and vortex for 0h 5m 0s at the minimum speed. Repeat the previous step 2 more times (4 times x 0h 5m 0s each filter)

Add 900µL of solution MBL. Dispense slowly; a fraction of the volume can be lost.

Before use, heat the MBL solution at 65°C for 0h 10m 0sas is suggested by the manufacturer.

Incubate the filter units vertically with the inlet upward at 90°Cfor 0h 5m 0sin an oven. Before and after the incubation, check for any leakage in the Parafilm; replace it if needed.

Let the filters cool down at room temperature for 0h 2m 0s, and re-tight the caps and check the Parafilm. Then, vortex at maximum speed for 0h 5m 0s. While mixing, check that the filters stay in place. If not, lower the speed.

Transfer the lysate from the filter unit to a 3-5mLsyringe; push 1 mL of air into the filter while it is vertical, and then release the plunger. Continue pulling back until the lysate is recovered in the syringe.

Pour the lysate into a 5mLPowerbeat tube and vortex horizontally for 0h 5m 0s at maximum speed

Centrifuge the tube at 4000x g,0h 0m 0sfor 0h 1m 0s

Carefully transfer the lysate to a clean 2.2mL collection tube. Then, add 1,6µL of RNAse (final concentration 100mg/mL). Incubate the samples at 37°C x 0h 30m 0s in a heating block or a water bath.

Add 300µL IRS solution to the tube and vortex. Then incubate at 4°C for 0h 5m 0s.

Centrifuge the tube at 13000x g,0h 0m 0sfor 0h 1m 0s

Transfer the supernatant to a 5mL collection tube, avoiding the pellet, and add 3mL of MR solution and vortex. Heat the MR solution at 65°Cfor 0h 10m 0s before using it.

A VacValve vacuum system and a vacuum pump are used for the following steps.

Load the supernatant (4,5mL) into a tube extender and MB spin column. Filtrate at low pressure. The column is attached to the VacValve vacuum system, as shown below.

Once the lysate passes through, the column extender is carefully removed. Next, wash the spin column with 800µLof ethanol. Keep the columns open.

Now, wash the spin column with 800µLof PW solution. Keep the columns open.

Allow the membrane to dry by keeping the vacuum pump running for 1 min.

Repeat step 21, and wash the spin column adding 800µLof ethanol. Allow the membrane to dry as before.

Place the spin column in a clean collection tube and dry it out by centrifugation at 13000x g,0h 0m 0s for

0h 2m 0s

Transfer the spin column to a new clean tube, and add 50-100µLof solution EB (or DNA-free grade

water). Centrifuge at 13000x g,0h 0m 0s for 0h 1m 0s.

Voila! The DNA is in the collection tube, ready for further processing.

The DNA purity is checked with a Nanodrop.

The DNA concentration is quantified by Qubit.