Feb 22, 2024
eDNA extraction from water samples filtered through 47 mm diameter filters (NucleoMag DNA/RNA Water Kit - MACHEREY NAGEL).
- Marine Vautier1,
- Cecile Chardon1,
- Cyrielle GALIEGUE1,
- Isabelle Domaizon1
- 1INRAE - Univ. Savoie Mont Blanc - UMR CARRTEL - Pole R&D Ecla
- CARRTEL
Protocol Citation: Marine Vautier, Cecile Chardon, Cyrielle GALIEGUE, Isabelle Domaizon 2024. eDNA extraction from water samples filtered through 47 mm diameter filters (NucleoMag DNA/RNA Water Kit - MACHEREY NAGEL).. protocols.io https://dx.doi.org/10.17504/protocols.io.j8nlkox7dv5r/v1
License: This is an open access protocol distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Protocol status: Working
We use this protocol and it's working
Created: February 22, 2024
Last Modified: February 22, 2024
Protocol Integer ID: 95601
Keywords: eDNA, water, Sterivex, DNA, extraction, filter, rare DNA, magnetapure 32 nucleic acid purification system, dna extraction, nucleic acid purification system, nucleic acid purification, reversible adsorption of nucleic acid, extraction from water sample, rna water kit, environmental dna, nucleomag dna, nucleic acid, nucleomagdna, extraction, water sample, dna, purification, rna, molecular biology analysis
Abstract
The objective of this protocol is the environmental DNA (eDNA) extraction from water samples filtered through 47 mm diameter filters. This protocol can be performed from filters preserved in tubes prefilled or not with preservation buffer.
DNA extraction is performed using a MagnetaPure 32 Nucleic Acid Purification System (Dutscher) and with the NucleoMagDNA/RNA Water Kit (Macherey Nagel).
The procedure is based on reversible adsorption of nucleic acids to paramagnetic beads under appropriate buffer conditions.
The benefits of using the MagnetaPure 32 Nucleic Acid Purification System (Dutscher) are increased productivity and repeatability, as well as eliminating human error and the pain of repetitive work.
This protocol is used prior to molecular biology analysis (e.g. qPCR, metabarcoding, ddPCR) to specifically target both macro- and micro-organisms eDNA extracted from water samples.
This protocol is optimised for rare eDNA and the suggested elution volumes are therefore low (between 50 and 65 µL), but can be increased if targets are more abundant.
Image Attribution
Marine Vautier
Guidelines
The main steps of the protocol are:
- Material preparation
- Plate preparation
- Sample lysis
- Extraction with the MagnetaPure 32 System (Dutscher)
- DNA elution
Materials
- Materials:
- 1000 µL pipette
- 100 µL pipette
- Scissors
- Vortex + benchtop centrifuge for 5 mL tubes
- Horizontal vortex with 5 mL tube holder (15 mL tube holders)
- Centrifuge for 2 mL tubes (relative centrifugal force needed: 11,000 x g)
- MagnetaPure 32 Nucleic Acid Purification System (Dutscher)
- Specific DNA-workstation (sterile area equipped with air filtration and UV systems)
- Consumables:
All tubes and tips must be sterile
- 1000 µL tips with filter
- 100 µL tips with filter
- 50 mL tubes: 4 to prepare aliquots and 3 for scissors decontamination
- 5 mL tubes: 1 per 8 samples to prepare NucleoMag B-Beads and MWA2 mix
- 2 mL tubes: 1 per sample to transfer lysate + 2 to prepare aliquots
- 1.5 mL tubes: 1 per sample to transfer eluted DNA
- 96-well plate with 2 mL deep-wells, U-Bottom (Macherey Nagel - 746032.DEEP): 1 per 16 samples
- Magnetic rod coverfor MagnetaPure 32 (Macherey Nagel – 747032.TC): 1 per 8 samples
- Plastic film to protect the 96-well plate
- Gloves
For any manipulation in a rare DNA room, provide complete equipment (disposable coat, cap, mask, shoe covers & gloves).
- Reagents:
- NucleoMag DNA/RNA Water kit (Macherey Nagel)
Note: shelf life of reagents for 24 months from production
- To clean the scissors:
o Solution to remove DNA (e.g.DNA-off, DNA away)
o Ethanol 96% for molecular biology
o Molecular biology grade water
- Samples to be extracted:
- Filters in 5 mL tubes prefilled with MWA1 buffer or not
Troubleshooting
Before start
- Filtration and preservation of the water samples through filters
This protocol can be performed from filters preserved in tubes prefilled or not with preservation buffer (e.g. MWA1). If the filter is not prefilled with buffer, it should be frozen immediately after water filtration and until DNA extraction.
Note: If the filters are preserved with MWA1 buffer, the extraction can be performed directly, but for other preservation buffers such as Longmire and CTAB, the protocol proposed here will work, but upstream precipitation is recommended to increase the extraction efficiency.
This protocole is suitable for the DNA extraction from different types of 47 mm diameter filters:
| Filter Type | |
| Polyethersulfone (PES) | |
| Polycarbonate (PC) | |
| Cellulose nitrate (NC) | |
| Cellulose mixed esters (CM) | |
| Cellulose acetate (CA) |
The filters should be preserved in 5 mL tubes for this DNA extraction protocol.
- The following precautions must be applied:
- Wear gloves throughout the extraction process
- Clean the bench with a DNA-removing solution (e.g. DNA-off, DNA away).
- Use tips with filters to avoid contaminations
- All steps have to be performed under a specific DNA-work station (sterile area equipped with air filtration and UV systems)
For any manipulation in a rare DNA room, provide complete equipment (disposable coat, cap, mask, shoe covers & gloves).
- Pre and post extraction equipment decontamination:
- Clean a specific DNA work station and apply UV
- MagnetaPure 32 System (Dutscher): Visual check for residues to be removed and UV decontamination – see instrument manual
- Scissors decontamination (to be done before starting the protocol, and between each filter cutting)
- Prepare :
- one 50 mL tube with DNA-removing solution (e.g. DNA-off, DNA away)
- one 50 mL tube with molecular biology grade water
- one 50 mL tube with ethanol
- Successively dip the scissors into each tube, opening and closing the scissors in each tube.
Note: The cutting of filters is not a requirement, but it does have an impact on the extraction efficiency.
Material preparation
- To limit contamination of the kit buffers, it is recommended to aliquote them:
- Into 50 mL tubes for MWA1, MWA2, MWA3 and MWA4
- Into 2 mL tubes for NucleoMag B-Beads solution and DNase-free H2O
- Tubes annotation
- one 2 mL tube per sample for lysate collection
- one 1.5 mL tube per sample for DNA collection
- one 5 mL tube per 8 samples for the NucleoMag B-Beads and MWA2 mix preparation
- Scissors decontamination (to be done before starting the protocole, and between each filter cutting)
- Prepare :
- one 50 mL tube with DNA-removing solution (e.g. DNA-off, DNA away)
- one 50 mL tube with molecular biology grade water
- one 50 mL tube with ethanol
- Successively dip the scissors into each tube, opening and closing the scissors in each tube.
Note: The cutting of filters is not a requirement, but it does have an impact on the extraction efficiency.
Plate preparation 1/2
In this step, the buffers provided by the kit are distributed in a 96-well plate.
For DNA extraction from filtered water samples, the 12 columns of the plate are divided into 2 sections of 6 columns each, allowing up to 16 samples to be extracted per plate.
- Annotate the 96-well plate as recommended below:
Table 1: Recommended plaque annotation
Note: It is useful to mark the dividing line between columns 6 and 7 with a marker pen to provide a visual cue for filling the plate.
- Add the appropriate buffers into the appropriate wells of the plate.
1stcolumn / 7thcolumn: Will be filled during plate preparation 2/2
2ndcolumn / 8thcolumn: 850 µL of MWA3 (1st wash)
3rdcolumn / 9thcolumn: 850 µL of MWA3 (2nd wash)
4thcolumn /10thcolumn: 850 µL of MWA4 (3rd wash and bead drying)
5thcolumn / 11thcolumn: not used
6thcolumn / 12thcolumn: 50 µL or 65 µL of DNase-free H2O (DNA elution)
Note: The choice of elution volume is based on the expected eDNA amount. The smaller the amount, the smaller the elution volume in order to obtain more concentrated DNA.
Table 2: Plate preparation 1/2
- Film and reserve the plate at Room temperature
30m
- Preparation of the NucleoMag B-Beads and MWA2 mix:
- Prepare one 5 mL tube / maximum 8 samples
- Add MWA2 only, the NucleoMag B-beads will be added during plate preparation 2/2 (allow a margin of one sample for the mix preparation. For example: plan a mix for 9 samples if 8 samples are to be extracted)
Table 3: Volume required to prepare NucleoMag B-beads and MWA2 mix (no margin)
5m
Sample Lysis
During this step, a mechanical and chemical lysis of the sample is performed.
- For samples prefilled with buffer:
- Collect the 5 mL tubes containing the filters
Note: If the tubes containing the filters are frozen, defrost them 00:10:00 atRoom temperature
- Cut the filter into small pieces directly into the tube using decontaminated scissors
Note: Scissors must be decontaminated between each sample (see section 1 "material preparation")
- Place the tubes on the vertical vortex 00:00:05 at median speed
- Place the tubes on the horizontal vortex 00:00:05 at maximum speed
- Place the tubes into the benchtop centrifuge
- Pipette the lysate from the tube and transfer it into a 2 mL tube
- Centrifuge at 11000 x g, 00:00:30
- Replace the tubes into the rack and reserve them at Room temperature until their distribution into the 96-well plate
- For samples without buffer:
- Collect the 5mL tubes containing the filters from the freezer and place On ice
- Add immediately 750 µL of MWA1 buffer into each tube
- Cut the filter into small pieces directly into each tube using decontaminated scissors
Note: Scissors must be decontaminated between each sample (see section 1 "material preparation")
- Place the tubes on the vertical vortex 00:00:05 at median speed
- Place the tubes on the horizontal vortex 00:00:05 at maximum speed
- Place the 5 mL tubes into the benchtop centrifuge
- Pipette the lysate from the tube (approximately 650 µL ) and transfer it into a 2 mL tube
- Centrifuge at 11000 x g, 00:00:30
- Replace the tubes into the rack and reserve them at Room temperature until their distribution into the 96-well plate
10m 20s
Plate preparation 2/2
- Preparation of the NucleoMag B-Beads and MWA2 mix
NucleoMag B-Beads and MWA2 mix sediment quickly, vortex between each samples to ensure homogeneity
- Vigorously vortex NucleoMag B-Beads tube
- For each tube containing MWA2 buffer (previously prepared), add the appropriate volume of NucleoMag B-Beads (see Table 3 above)
- Vortex
- NucleoMag B-Beads - MWA2 mix and lysate distribution
- Remove the film from the plate
- Add the appropriate solution into each well of the plate
1stcolumn / 7thcolumn:
500 µL of NucleoMag B-Beads and MWA2 mix
450 µL of Lysate (supernatant from the 2 mL tubes)
Table 4: Plate preparation 2/2
15m
Extraction step performed in the MagnetaPure 32 System
- Place the plate into the MagnetaPure 32 System and insert the magnetic rod coverfor – see instrument manual
- Select the appropriate program to the chosen elution volume and elution temperature
Table 5: MagnetaPure 32 System program for NucleoMag DNA/RNA Water Kit DNA extraction
Note: Heating to 56°C during elution gives a higher yield of DNA, but there is a risk of evaporation which reduces the volume of eluted DNA recovered
- Start the run (The run lasts approximately 00:40:00 )
40m
Transfer of DNA extracts
30m
- At the end of the run, remove the plate and place it into the DNA-workstation
- Remove the magnetic rod cover and start UV for decontamination – see instrument manual
- In the DNA-workstation, transfer each DNA extract into a 1.5 mL tube previously annotated
Note: DNA concentration and quality can be measured at this step (e.g. Nanodrop)
- Store DNA extracts at 4 °C for immediate use, or at -20 °C or -80 °C for long-term preservation
Protocol references
NucleoMag DNA/RNA Water kit (Macherey Nagel) manual : https://www.mn-net.com/media/pdf/ce/b5/38/Instruction-NucleoMag-DNA-RNA-Water.pdf
MagnetaPure 32 Nucleic Acid Purification System (Dutscher) manual : https://pdf.dutscher.com/doc/255743/255743_MEen.pdf