RNA extraction from wastewater for detection of SARS-CoV-2
Livia C T Scorza, David Findlay, Julie Bolland, Brindusa Cerghizan, Kirsty Campbell, David Thomson, Alexander Corbishley, David Gally, Stephen Fitzgerald, Alison Tidswell, Sean McAteer
Wastewater-based epidemiology
Infectious diseases
Public health
RNA extraction
RNA viruses
Covid-19
SARS-CoV-2
Abstract
As part of the global response to the 2019 novel Coronavirus (SARS-CoV-2) pandemic, it was determined that SARS-CoV-2 RNA was detectable in the faeces of both symptomatic and asymptomatic patients (1). Further analysis demonstrated that a wastewater epidemiological (WWE) approach, similar to that used to track other viruses (i.e. Poliovirus), could be employed to monitor the spread of SARS-CoV-2. The presence of, or changes in concentration of viral RNA within the wastewater network can assist in monitoring the emergence of further viral peaks (2). Thus, monitoring the spread of Covid-19 using the WWE approach has been extensively explored in several countries (3). This procedure, developed by the Scottish Environment Protection Agency (SEPA) based upon work of the Corbishley group at the Roslin Institute, University of Edinburgh, outlines the method for the concentration of viral RNA in wastewater, as well as in other types of environmental and potable water samples.In this method, a known volume of sample is concentrated using a centrifugal filter to allow further extraction and detection of SARS-CoV-2 RNA.For further analysis using RT-qPCR please search for "RT-qPCR for detection of SARS-CoV-2 in wastewater" by the same authors of this protocol on protocols.io References:1. Jones, D. L., Baluja, M. Q., Graham, D. W., Corbishley, A., McDonald, J. E., Malham, S. K., Hillary, L. S., Connor, T. R., Gaze , W. H., Moura , I. B., Wilcox, M. H., & Farkas , K. (2020).Shedding of SARS-CoV-2 in feces and urine and its potential role in person-to-person transmission and the environment-based spread of COVID-19. Science of the Total Environment .https://doi.org/10.1016/j.scitotenv.2020.1413644.2. Fitzgerald, S., Rossi, G., Low, A., McAteer, S., O’Keefe, B., Findlay, D., Cameron, G. J., Pollard, P., Singleton, P. T. R., Ponton, G., Singer, A. C., Farkas, K., Jones, D., Graham, D. W., Quintela-Baluja, M., Tait-Burkard, C., Gally, D., Kao, R., & Corbishley, A.(2021).Site specific relationships between COVID-19 cases and SARS-CoV-2 viral load in wastewater treatment plant influent. Environmental Science and Technology . https://doi.org/10.1021/acs.est.1c050293. Wastewater SARS Public Health Environmental Response (W-SPHERE). https://sphere.waterpathogens.org/about
Before start
All sample processing is to be carried out within a Class II microbiological safety cabinet . * For all centrifugation steps, samples must be placed in centrifuge buckets or directly into a rotor and sealed prior to removal from the cabinet.
- All spin steps to be carried out at 4 ºC unless otherwise stated.
- Samples should be processed as soon as possible after collection but if this is not possible may be stored at 4˚C for up to 72 hrs . Upon receipt, samples are aliquoted (2x 50ml) and stored at -80˚C , to protect nucleic acid integrity, until ready for analysis.
Steps
Sample preparation
Clean all surfaces with 0.5% Sodium Hypochlorite (10% bleach) before and after use. Rinse with water to remove any residue.
If necessary defrost samples at 4°C
Add a known quantity of Sample Process Control RNA (PRRS) to each sample (view guidelines for more information).
Remove solid matter from wastewater samples by centrifugation at 4669x g,4°C
Carefully transfer the supernatant to a clean tube taking care not to disturb the pellet. Discard pellet.
RNA Concentration
Transfer 15ml of the clarified supernatant from the previous step to a 15 ml Amicon/Centricon Filter (10kDa)
Concentrate samples ~ by centrifugation (1500x g,4°C)
Check the level of the concentrate in the filter device by transferring the concentrate to a pre-weighed tube and re-weighing the tube to determine the concentrate volume
If <250 uL proceed to RNA extraction
If >250 uL and < 1ml give tubes a further 10 minutes at 4000 x g.
If >1ml give tubes a further 15minutes at 4000 x g.
Remove concentrated sample, using a side to side pipettor motion to ensure maximum recovery, and transfer to a pre-weighed 2ml tube
Weight tube plus concentrate and record concentrate volume.
Samples should be processed immediately after concentration. If this is not possible then they must be stored, immediately at -80°C until extraction can be carried out.
Extract viral RNA using QA_Viral_RNA_Mini.pdf according to next steps guidelines. Final elution in 60 µl AE buffer
Viral RNA Purification (Spin Protocol- QIAamp Viral RNA Mini Kit)
Prepare the reagents supplied in the kit according to manufacturer's guidelines and equilibrate buffers and sample at room temperature before starting:
Carrier RNA preparation:* Add 310 µl Buffer AVE to carrier RNA to obtain 1 µg/µl solution.
- Divide into 100 µl, single-use aliquots and store at -20°C. Do not freeze/thaw more than 3 times.
- 5.6 µl of carrier RNA-AVE is required per sample.
- For one sample, add 5.6 µl of carrier RNA-AVE to 0.56 ml of AVL buffer.
- For more than one sample, calculate the volume of Buffer AVL–carrier RNA mix needed per batch of samples (check Table 1 of QIAamp® Viral RNA Mini Handbook)
Resuspend buffer AW1 in ethanol (96-100%) – 130ml for 250 prep kit, 25ml for 50 prep kit.
Resuspend buffer AW2 in ethanol (96-100%) – 160ml for 250 prep kit, 30ml for 50 prep kit.
Before starting, ensure that buffer AVE and samples are equilibrated toRoom temperature
*Add an extraction blank as part of each analytical run .
*An optional positive control containing know quantities of SARS-CoV-2 and PRRS RNA can be included to determine extraction efficiency.
Transfer sample concentrate (to a maximum volume of 560µL) to a 1.5 ml tube, add 4x concentrate volume of AVL buffer containing carrier RNA and pulse-vortex for 15 seconds.
Incubate at room temperature for 10 minutes. Room temperature
Add same volume of ethanol, as AVL, per sample and pulse-vortex to mix for 15 seconds.
Carefully transfer up to 700 µl to QIAamp mini column (in 2ml collection tube) without wetting the rim. Close cap and spin at 6000x g
Discarding flow-through after each spin, repeating the previous step until sample is fully processed.
Carefully add 500 µl buffer AW1 to the mini columns. Close cap and spin at 6000x g. Discard the flow-through.
Add 500 µl of buffer AW2 to the mini columns. Close cap and spin at maximum speed for 0h 3m 0s
Transfer the mini-columns to a clean collection tube and spin at maximum speed for 0h 1m 0s .
Transfer to a clean tube and add 60 µl (1 spin) or 40µl (2 spins) of AVE and incubate at room temperature for 0h 1m 0s
Centrifuge at6000x g (or up to 13000 g)
If performing a 2x 40 µl spin elution, repeat steps 22 and 23.
RNA is now ready for RT-qPCR.
NB Performing a single-spin elution should generate ~50µl of RNA in suspension whereas 2 spins should produce ~70 µl and may increase RNA yield by up to 10%.
Record final elution volume.
Determination of yield
"Yields of viral RNA isolated from biological samples are normally less than 1 µg and therefore difficult to determine photometrically. Keep in mind that the carrier RNA (5.6 µg per 140 µl sample) will account for most of the RNA present. Quantitative RT-PCR is recommended for determination of viral RNA yield" (from QIAamp® Viral RNA Mini Handbook)
Proceed with RT-qPCR for detection of SARS-CoV-2.
For further analysis using RT-qPCR please search for "RT-qPCR for detection of SARS-CoV-2 in wastewater" by the same authors of this protocol on protocols.io
