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Virus concentration from environmental water and wastewater samples is a challenging task, carried out primarily for the identification and quantification of viruses. While several virus concentration methods have been developed and tested, we demonstrate here the effectiveness of ultrafiltration and skimmed milk flocculation for RNA viruses with different sample types.
Water and wastewater-based epidemiology have emerged as alternative methods to monitor and predict the course of outbreaks in communities. The recovery of microbial fractions, including viruses, bacteria, and microeukaryotes from wastewater and environmental water samples is one of the challenging steps in these approaches. In this study, we focused on the recovery efficiency of sequential ultrafiltration and skimmed milk flocculation (SMF) methods using Armored RNA as a test virus, which is also used as a control by some other studies. Prefiltration with 0.45 µm and 0.2 µm membrane disc filters were applied to eliminate solid particles before ultrafiltration to prevent the clogging of ultrafiltration devices. Test samples, processed with the sequential ultrafiltration method, were centrifuged at two different speeds. An increased speed resulted in lower recovery and positivity rates of Armored RNA. On the other hand, SMF resulted in relatively consistent recovery and positivity rates of Armored RNA. Additional tests conducted with environmental water samples demonstrated the utility of SMF to concentrate other microbial fractions. The partitioning of viruses into solid particles might have an impact on the overall recovery rates, considering the prefiltration step applied before the ultrafiltration of wastewater samples. SMF with prefiltration performed better when applied to environmental water samples due to lower solid concentrations in the samples and thus lower partitioning rates to solids. In the present study, the idea of using a sequential ultrafiltration method arose from the necessity to decrease the final volume of the viral concentrates during the COVID-19 pandemic, when the supply of the commonly used ultrafiltration devices was limited, and there was a need for the development of alternative viral concentration methods.
Determining the effective concentration of microorganisms in surface and wastewater samples for microbial community analysis and epidemiology studies, is one of the important steps for monitoring and predicting the course of outbreaks in communities1,2. The COVID-19 pandemic, unfolded the importance of improving concentration methods. COVID-19 emerged in late 2019 and, as of March 2023, still poses a threat to human health, social life, and the economy. Effective surveillance and control strategies to alleviate the impacts of COVID-19 outbreaks in communities have become an important research topic, ....
1. Comparison of serial ultrafiltration and skimmed milk flocculation to concentrate viruses in wastewater samples
Evaluation of viral RNA concentration methods
All six samples processed with UF-3k x g were positive and resulted in a 13.38% ± 8.14% recovery (Figure 1). Only one sample was positive when the samples were processed with UF-7.5k x g. All samples processed with SMF were positive and resulted in a 15.27% ± 2.65% recovery (Figure 1). The average recovery rates of UF-3K x g and SMF were significantly and co.......
One of the critical steps in this study is the elimination of solid particles by applying a prefiltration step with 0.2 µm and 0.45 µm membrane filters. Considering the partitioning of viruses into solid particles, especially enveloped viruses, prefiltration can cause a significant loss in viral recovery30. While a prefiltration step for ultrafiltration methods is almost always necessary for environmental and wastewater samples to prevent ultrafiltration devices from clogging, prefiltrat.......
This work was supported by NSERC Alliance Covid-19 Grant (Award No. 431401363, 2020-2021, Drs. Yuan and Uyaguari-Díaz). MUD would like to thank the University Research Grants Program (Award No. 325201). Both JF and JZA are supported by the Visual and Automated Disease Analytics (VADA) graduate training program. KY and JF both received fellowships from the Mitacs Accelerate program. MUD and his laboratory members (KY, JF, JZA) are supported by NSERC-DG (RGPIN-2022-04508) and the Research Manitoba New Investigator Operating grant (No 5385). Special thanks to the City of Winnipeg, Manitoba. This research was conducted at the University of Manitoba. We would like to ....
Name | Company | Catalog Number | Comments |
0.2 M sodium phosphate buffer with a pH 7.5 | Alfa Aesar | J62041AP | Fisher Scientific, Fair Lawn, NJ, USA |
0.2 μm 47-mm Supor-200 membrane disc filters | VWR | 66234 | Pall Corporation, Ann Arbor, MI |
0.45 μm 47-mm Supor-200 membrane disc filters | VWR | 60043 | Pall Corporation, Ann Arbor, MI |
4X TaqMan Fast Virus 1-Step Master Mix | Thermo Fisher Scientific | 4444432 | Life Technologies, Carlsbad, CA, USA |
Armored RNA Quant IPC-1 Processing Control | Asuragen | 49650 | Asuragen, Austin, TX, USA |
Brand A, Jumbosep Centrifugal Device, 30-kDa | Pall | OD030C65 | Pall Corporation, Ann Arbor, MI |
Brand B, Microsep Advance Centrifugal Device, 30-kDa | Pall | MCP010C46 | Pall Corporation, Ann Arbor, MI |
Centrifuge tubes (50 ml) | Nalgene | 3119-0050PK | Thermo Fisher Scientific |
DNAse I | Invitrogen | 18047019 | Thermo Fisher Scientific |
Dyna Mag-2 | Invitrogen | 12027 | Thermo Fisher Scientific |
GWV High Capacity Groundwater Sampling Capsules - 0.45 µm | Pall | 12179 | Pall Corporation, Ann Arbor, MI |
Hydrochloric acid, 1N standard solution | Thermo Fisher Scientific | AC124210025 | Fisher Scientific, Fair Lawn, NJ, USA |
MagMAX Microbiome Ultra Nucleic Acid Isolation Kit | Applied biosystems | A42358 | Thermo Fisher Scientific |
Nuclease free water | Promega | P1197 | Promega Corporation, Fitchburg, WI, USA |
Peristaltic pump | Masterflex, Cole-Parmer instrument | 7553-20 | Thermo Fisher Scientific |
pH meter | Denver instrument | RK-59503-25 | Cole-Parmer. This product has been discontinued |
Phenol:chloroform:isoamyl alcohol 25:24:1 | Invitrogen | 15593031 | Fisher Scientific, Fair Lawn, NJ, USA |
Primers and probe sets | IDT | Integrated DNA Technologies, Inc., Coralville, IA, USA | |
Qiagen All-prep DNA/RNA power microbiome kit | Qiagen | Qiagen Sciences, Inc., Germantown, MD, USA | |
QuantStudio 5 Real-Time PCR System | Thermo Fisher Scientific | A34322 | Life Technologies, Carlsbad, CA, USA |
Qubit 1X dsDNA High Sensitivity (HS) assay kit | Invitrogen | Q33231 | Thermo Fisher Scientific |
Qubit 4 Fluorometer, with WiFi | Invitrogen | Q33238 | Thermo Fisher Scientific |
Qubit RNA High Sensitivity (HS) assay kit | Invitrogen | Q32855 | Thermo Fisher Scientific |
RNAse A | Invitrogen | EN0531 | Thermo Fisher Scientific |
RNeasy PowerMicrobiome Kit | Qiagen | 26000-50 | Qiagen Sciences, Inc., Germantown, MD, USA |
Skim milk powder | Difco (BD Life Sciences) | DF0032173 | Fisher Scientific, Fair Lawn, NJ, USA |
Sodium phosphate buffer | Alfa Aesar | Alfa Aesar, Ottawa, ON, Canada | |
Synthetic seawater | VWR | RC8363-1 | RICCA chemical company |
Synthetic single-stranded DNA gBlock | IDT | Integrated DNA Technologies, Inc., Coralville, IA, USA | |
VacuCap 90 Vacuum Filtration Devices - 0.1 µm, 90 mm, gamma-irradiated | Pall | 4621 | Pall Corporation, Ann Arbor, MI |
VacuCap 90 Vacuum Filtration Devices - 0.2 µm, 90 mm, gamma-irradiated | Pall | 4622 | Pall Corporation, Ann Arbor, MI |
β-mercaptoethanol | Gibco | 21985023 | Fisher Scientific, Fair Lawn, NJ, USA |
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