Skip to main content
Elsevier - PMC COVID-19 Collection logoLink to Elsevier - PMC COVID-19 Collection
. 2021 Aug 19;801:149757. doi: 10.1016/j.scitotenv.2021.149757

Wastewater SARS-CoV-2 monitoring as a community-level COVID-19 trend tracker and variants in Ohio, United States

Yuehan Ai a, Angela Davis b, Dan Jones c,e, Stanley Lemeshow d, Huolin Tu c, Fan He a, Peng Ru c, Xiaokang Pan e, Zuzana Bohrerova f, Jiyoung Lee a,b,
PMCID: PMC8373851  PMID: 34467932

Abstract

The global pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has resulted in more than 129 million confirm cases. Many health authorities around the world have implemented wastewater-based epidemiology as a rapid and complementary tool for the COVID-19 surveillance system and more recently for variants of concern emergence tracking. In this study, three SARS-CoV-2 target genes (N1 and N2 gene regions, and E gene) were quantified from wastewater influent samples (n = 250) obtained from the capital city and 7 other cities in various size in central Ohio from July 2020 to January 2021. To determine human-specific fecal strength in wastewater samples more accurately, two human fecal viruses (PMMoV and crAssphage) were quantified to normalize the SARS-CoV-2 gene concentrations in wastewater. To estimate the trend of new case numbers from SARS-CoV-2 gene levels, different statistical models were built and evaluated. From the longitudinal data, SARS-CoV-2 gene concentrations in wastewater strongly correlated with daily new confirmed COVID-19 cases (average Spearman's r = 0.70, p < 0.05), with the N2 gene region being the best predictor of the trend of confirmed cases. Moreover, average daily case numbers can help reduce the noise and variation from the clinical data. Among the models tested, the quadratic polynomial model performed best in correlating and predicting COVID-19 cases from the wastewater surveillance data, which can be used to track the effectiveness of vaccination in the later stage of the pandemic. Interestingly, neither of the normalization methods using PMMoV or crAssphage significantly enhanced the correlation with new case numbers, nor improved the estimation models. Viral sequencing showed that shifts in strain-defining variants of SARS-CoV-2 in wastewater samples matched those in clinical isolates from the same time periods. The findings from this study support that wastewater surveillance is effective in COVID-19 trend tracking and provide sentinel warning of variant emergence and transmission within various types of communities.

Keywords: Wastewater-based epidemiology, PMMoV, crAssphage, Quadratic polynomial model, N501Y, B.1.427/429, D614G

Graphical abstract

Unlabelled Image

1. Introduction

Community and intrafamily transmission is one of the most common modes of human-to-human transmission of SARS-CoV-2, which can occur before the confirmation of a clinical diagnosis (Hu et al., 2021; World Health Organization (WHO), 2021; Liu et al., 2020; He et al., 2020). For more effective control and timely monitoring of the outbreaks, wastewater-based SARS-CoV-2 surveillance has been implemented as a complementary tool for the COVID-19 surveillance system (Hart and Halden, 2020; Odh, 2021). Wastewater-based epidemiology (WBE) has been employed to monitor a variety of pathogenic viruses around the world such as Polio, Dengue, Norovirus, and SARs-CoV (Sims and Kasprzyk-Hordern, 2020). WBE targets the DNA/RNA residue from viruses, which serve as a population biomarker of the pathogen. Not like other respiratory viruses, SARS-CoV-2 is found in the gastrointestinal tracts and stools of the majority of infected people (Cheung et al., 2020; Wang et al., 2020). The discharged virus has been detected in wastewater streams at the early stages of the pandemic and even before the first recorded case in the population surveyed (Medema et al., 2020; Nemudryi et al., 2020; Randazzo et al., 2020; Wurtzer et al., 2020). With the analysis of viral signals in population-pooled wastewater samples, WBE can provide early warnings of COVID-19 emergence at a community level (Ahmed et al., 2020a; Lodder and Husman, 2020; G.L. Rosa M. Iaconelli P. Mancini G.B. Ferraro L. Bonadonna L. Lucentini E Suffredini, n.d.; F. Wu J. Zhang A. Xiao X. Gu W.L. Lee F. Armas K. Kauffman W. Hanage M. Matus N. Ghaeli N. Endo C. Duvallet M. Poyet K. Moniz A.D. Washburne T.B. Erickson P.R. Chai J. Thompson E.J. Alm, 2020).

The WBE surveillance of COVID-19 is advantageous in many other ways. Firstly, with approximately 105,600 wastewater treatment plants operating globally, 27% of the global population can benefit from health information provided by WBE (Hart and Halden, 2020). Wastewater can capture signals from symptomatic as well as pre-symptomatic/asymptomatic carriers, which tend to be under-detected by clinical tests. Secondly, wastewater provides a longer detection window for the SARS-CoV-2 carriers since RNA signals in fecal samples showed longer persistency than in oropharyngeal swabs (Wang et al., 2020). Thirdly, it is hard to gain a “real-time” picture of the pandemic from clinical screening due to backlogs of test results up to 10 days (Kevin, 2020; Richterich, 2020). WBE is capable of generating results in a real-time manner with a relatively low cost compared to individual clinical testing, enabling the decision-makers to identify outbreak hotspots and take timely actions (Ahmed et al., 2021). Moreover, WBE can aid in monitoring the epidemic progression by giving reliable information on the effectiveness of intervention strategies. As several SARS-CoV-2 variants have emerged, some studies successfully employed WBE to investigate the circulating viral variants in the wastewater through high-throughput sequencing (Fontenele et al., 2021; Jahn et al., 2021; Martin et al., 2020). Therefore, WBE has been adopted as a COVID-19 trend tracker and more recently for detecting variants by public health authorities in the United States.

At present, most wastewater-associated studies have focused on municipal wastewater and covered a relatively short period of time at the early stages of the pandemic. In an effort to help with the long-term monitoring of the spread of COVID-19 across the state of Ohio, the Ohio Department of Health (ODH), the Ohio Environmental Protection Agency (Ohio EPA), and Ohio Water Resources Center (Ohio WRC) at The Ohio State University established the Ohio Coronavirus Wastewater Monitoring Network (Odh, 2021) using participating laboratories in Ohio. The present study contributes to the network by generating critical wastewater-based information for the populations in nine sewage catchments in central Ohio, including the largest city, Columbus, and other urban and rural areas. A quantitative method was developed and validated for the measurement of SARS-CoV-2 gene targets in wastewater samples. To further evaluate the feasibility of using WBE as a predicting/modeling tool for the COVID-19 outbreak dynamics, correlations between the concentrations of SARS-CoV-2 genes in wastewater and the clinical COVID-19 case numbers in their corresponding sewershed areas were investigated. In order to compensate for the fluctuation in fecal material caused by dilution, we investigated normalization methods with two of the most prevalent human fecal viral indicators, pepper mild mottle virus (PMMoV) and cross-assembly phage (crAssphage) (Jahn et al., 2021; Daughton, 2012; Greaves et al., 2020; Hamza et al., 2011; Malla et al., 2019; Symonds et al., 2018). Moreover, this study explored whether the wastewater matrix can serve as a sentinel piece for detecting SARS-CoV-2 variants of concern within a community.

2. Materials and methods

2.1. Sampling sites and wastewater collection

Nine wastewater treatment plants (WWTPs) in central Ohio were involved in this study. Two of the WWTPs (Jackson Pike and Southerly) serve different catchments in Columbus, which is the largest city in Ohio with a population of around 900,000 (U.S. Department of Commerce, 2019). The sewersheds of the other wastewater facilities cover 7 smaller Ohio cities (Athens, Circleville, Lancaster, Marietta, Marysville, Newark, and Zanesville) in urban and rural areas with population ranges from 14,000 to 49,000 (U.S. Department of Commerce, 2019). Confirmed COVID-19 case numbers and the boundaries of all 9 sewershed catchments vary (Fig. 1 ), and details on the serving population and operating characteristics of the WWTPs are summarized (Table 1 ). Approximately one liter of 24-h composite samples were collected from the WWTPs twice a week, representing the untreated wastewater influent of Sunday and Tuesday. The sampling period started in late July 2020, with varied starting dates among sites, and ended at the first week of January 2021. Wastewater samples obtained from Jackson Pike, Southerly, and Newark WWTPs were delivered to the lab and processed on the sampling day. Samples from the other utilities were shipped on ice overnight and processed on the following day. Samples were immediately stored at 4 °C until further processing. Samples that were delayed in their shipment and subjected to temperature abuse (>10 °C) were not processed.

Fig. 1.

Fig. 1

Geographic boundaries and locations of nine sewersheds and cumulative confirmed COVID-19 case numbers.

Table 1.

Summary of WWTP operating characteristics and each sewershed population with confirmed case numbers during the study period.

WWTP name City County Sewer type Average flowrate (MGD) Population served Cumulative confirmed casesa Cumulative incidence (cases /100,000 residents)
Jackson Pike Columbus Franklin Combined 82 645,940 41,557 6434
Southerly Columbus Franklin Combined 130.4 654,817 46,248 7063
Athens Athens Athens Separate 2.6 24,536 1523 6207
Circleville Circleville Pickaway Separate 2.01 13,965 692 4955
Lancaster Lancaster Fairfield Combined 7.67 24,303 2616 10,764
Marysville Marysville Union Separate 4.37 24,677 2166 8777
Marietta Marietta Washington Separate 2.84 15,284 842 5509
Newark Newark Licking Combined 9 45,000 2889 6420
Zanesville Zanesville Muskingum Combined 5.8 47,500 2653 5585
a

Cumulative confirmed cases from the beginning of the pandemic to 01/02/2021.

2.2. Wastewater processing: virus filtration and concentration

To concentrate virus from wastewater samples, two approaches were used after optimization. Initially, an adsorption-precipitation-based method was adopted. Virus was first adsorbed and eluted from a positively charged filter unit (ViroCap, Scientific Methods, Inc., Granger, IN, USA), followed by concentrating via organic flocculation and centrifugal ultrafiltration (Supplementary Method S1) (Bennett et al., 2010). For faster turnaround, from the second month of the study, we employed a protocol consisting of solid removal and viral concentration. Each wastewater sample was processed in duplicate. First, 100 mL of raw wastewater with 0.05% Tween-20 were centrifuged at 4 °C, 2,500 × g for 10 min for large solid removal. Small debris and bacteria were further removed by filtering the supernatant using a 0.45 μM sterile filter unit (Milipore, Burlington, MA, USA). Then, the filtrate was concentrated using a 0.05 μm Hollow Fiber Polysulfone Concentrating Pipette Select tips (Innovaprep, Drexel, MO, USA). Approximately 200 μL of viral concentrate was then eluted following the manufacturer's instruction with some modifications (Innovaprep, 2020): valve open for 600 ms, 1 pulse, foam factor of 10, valve start time of 3.0 s, flow end of 10 s, flow minimum start time of 40 s, delay of 3.0 s, pump at 25%, pump delay time of 1 s, and stored at −80 °C for downstream analysis. Recovery efficiency of the method was evaluated by spiking with three different surrogates: male specific coliphage MS2 (ATCC cat. No. 15597-B1), bovine coronavirus (BCoV strain ML-6 mebus), and human coronavirus OC43 (ATCC cat. No. VR-1558) (Bae and Schwab, 2008; Cimolai, 2020).

2.3. RNA/DNA extraction and RT-ddPCR analysis

Nucleic acid was extracted from the viral concentrate using an RNeasy PowerMicrobiome Kit (QIAGEN, Germantown, MD, USA). Reverse transcription was conducted with the High-Capacity cDNA Reverse Transcription Kit (Applied Biosystems, Pittsburgh, PA, USA). 3 μL cDNA was applied to the quantification of SARS-CoV-2 genome equivalents using a droplet digital PCR (ddPCR) platform (Bio-rad QX200 system). Three ddPCR assays were developed to target two nucleocapsid (N) gene regions and the envelope (E) gene of SARS-CoV-2. The N gene region assays employed two primers/probe sets from U.S. Centers for Disease Control and Prevention (CDC), amplifying the N1 and N2 regions (Hirotsu et al., 2020; Jung et al., 2020). The E gene assay is based on the E_Sarbeco primers/probe set recommended by WHO (Corman et al., 2020). Quantifications for three SARS-CoV-2 surrogates (MS2, BCoV, and OC43) and two human fecal indicators (PMMoV and crAssphage) were also conducted with diluted cDNA (Dare et al., 2007; Decaro et al., 2008; Haramoto et al., 2013; Ogorzaly and Gantzer, 2006; Stachler et al., 2017). The reaction mixture (20 μL) contains ddPCR supermix for probes (Bio-Rad, Hercules, CA, USA), DNase- & RNase-free water, 900 nM of forward and reverse primers, 250 nM of probe, and templates. Firefly (Coleoptera) Luciferase control RNA (Promega, Madison, WI, USA) was implemented as an internal amplification control for the detection of PCR inhibition (Johnson et al., 2005). ddPCR mixture with or without wastewater cDNA template were spiked with an equal titer of Luciferase cDNA. PCR inhibition was assessed by comparing the difference in Luciferase gene amplification. Primer/probe sequences and ddPCR parameters used in this study are summarized (Table S1). Briefly, after droplet generation using the QX200 Droplet Generator, target genes were amplified with a Bio-Rad C1000 Touch Thermal Cycler. The cycling conditions included an initial denaturing step at 94 °C for 10 min, followed by 40–45 cycles of 94 °C for 30 s and annealing for 60 s. A final incubation step was performed at 98 °C for 10 min and then a final hold of 4 °C. After amplification, gene concentrations were quantified using a QX200 droplet reader and QuantaSoft (V 1.7; Bio-Rad). Two technical replicates were performed for each ddPCR assay.

2.4. Quantification and statistical analysis

COVID-19 case numbers were retrieved from ODH COVID-19 Dashboard (Odh, 2021), reflecting the absolute confirmed case counts of the sewersheds targeted by the estimated symptom onset date. The boundaries of the sewersheds were mapped with Tableau (V 2020.1) (Fig. 1). 3-day, 5-day, and 7-day moving averages were calculated from the case numbers using “zoo” package in RStudio (V 1.3.1093). All other plots were generated with “ggplot” package in Rstudio. Target gene copy numbers were calculated as the mean of four replicates (two biological and two technical replicates). The limit of quantification (LOQ) of ddPCR assay is two gene copies/reaction. For detectable-but-not-quantifiable measurements, the results are recorded as one-half of the LOQ. All statistical analyses were performed in RStudio using “ggpubr”, “stats”, and “rstatix” packages. A p-value < 0.05 is considered statistically significant. The strength of a linear association was first assessed through a Pearson correlation coefficient. All essential assumptions were examined (normality and linearity). SARS-CoV-2 RNA concentrations and case counts were fitted into a linear model. Spearman's non-parametric correlation coefficients were also computed since they were less dependent on the underlying distributions being normal. Additionally, polynomial regressions models were fit. Significance of regression models was assessed via the F-test.

2.5. SARS-CoV-2 genome sequencing and variant analysis

A subset of samples of early January 2021 was selected for next-generation sequencing (NGS) by hybridization and/or amplicon methods. For probe-bait NGS, extracted RNA underwent 1st and 2nd strand cDNA synthesis (NEBNext® Ultra# II Non-Directional RNA Second Strand Synthesis Module, NEB, Ipswich, MA). Library construction was performed with KAPA Hyper Prep with KAPA HiFi HotStart Library Amplification Kit (Roche Diagnostics, Indianapolis, IN), with subsequent hybridization with SARS-CoV-2 bait probes (IDT, Coralville, CA) and were then sequenced on NextSeq (Illumina, San Diego, CA). Amplicon sequencing was performed using the CovidSeq kit and sequenced on NextSeq. Analysis tools include custom pipelines utilizing GATK and Mutect2 (Broad Institute) and Dragen SARS-COVID variant detection (Illumina). Viral sequences were strain-typed using Pangolin (Rambaut et al., 2020) and NextStrain criteria (T. Bedford E. Hodcroft R. Neher, n.d.).

For comparison with wastewater findings, sequencing of nasal or nasopharyngeal swab extracted RNA from SARS-CoV-2 positive PCR samples from The Ohio State University Wexner Medical Center was performed. The laboratory received samples from sites across central Ohio, including all sites in this survey except Athens and Marietta. NGS was performed with CovidSeq as above or using the AmpliSeq SARS-CoV-2 Research Panel on Ion Chef-S5 instruments (Thermofisher, Waltham, MA). The lower limit of detection of a variant for the amplicon methods was approximately 5% variant fraction at a mean depth of 200-1000 reads.

3. Results and discussion

3.1. Performance of the wastewater concentrating and detection methods

A variety of methods have been adopted around the world to concentrate and quantify SARS-CoV-2 from wastewater. The reliability, reproducibility, and sensitivity of these methods needs to be validated to make better use of wastewater data (Consortium, S.-C.-2 I, et al., 2021). The performance of the two viral filtration and concentration methods in this study was evaluated by monthly recovery efficiency tests with three SARS-CoV-2 surrogates. MS2 is a non-enveloped bacteriophage widely used as a surrogate for viral pathogens (Dawson et al., 2005; Lin and Marr, 2017). For a better understanding of the efficiency of the methods on SARS-CoV-2, two other enveloped coronaviruses (BCoV and OC43) were used in this study. The Concentrating Pipette (CP)-based concentration method was more effective than the ViroCap-based method, especially in recovery efficiency and speed. The time needed for the CP protocol was ten times shorter than the ViroCap-based method. The recovery efficiency of MS2 with the CP method (53.6%) was two times higher than that with the ViroCap-based method (24.7%). ViroCap was less effective in recovering enveloped coronaviruses from wastewater (BCoV: 7.2%). The recovery efficiency of BCoV with the CP-based method varied among the samples tested (ranged from 16.8% to 53.2%), indicating that the efficiency may be dependent on the characteristics of the wastewater matrix, such as the solid contends (Ahmed et al., 2020b). To enhance the recovery efficiency and shorten the processing time, we switched to the CP-based protocol after the first month. One potential concern of this rapid CP method was that solids are removed prior to virus concentration. Since a previous study found that enveloped viruses tend to be more associated with the surface of solids in wastewater than non-enveloped viruses (Ye et al., 2016), the partitioning of the coronavirus surrogates in sample fractions was investigated for our methods. In the spiking test, only <0.2% of the BCoV was recovered from the pellet after centrifugation. Compared to the spiked BCoV, SARS-CoV-2 probably had longer residence time in wastewater, thus, higher percentage of SARS-CoV-2 (~10%) was found in the pellet portion. Since the majority (~90%) of SARS-CoV-2 RNA signal was detected in the viral concentrate, the virus in the solid (pellet) portion of wastewater was not included in this study.

For accurate quantification of SARS-CoV-2 gene concentration, presence of PCR inhibition in the samples should be checked. In our study, no PCR inhibition was detected. It might be due to two reasons: the Qiagen kit used for RNA extraction includes several inhibitor removal steps; and ddPCR is more robust in handling inhibition-prone environmental samples than conventional quantitative PCR (Sedlak et al., 2014).

3.2. SARS-CoV-2 gene concentrations in wastewater

During this 5-month study, three SARS-CoV-2 genes (N1 and N2 gene regions, and E gene) were detected in all 250 wastewater influents, with concentrations ranging from 1 × 102 to 1 × 105 gene copies/L of wastewater. The overall observed trend was that the SARS-CoV-2 gene concentrations stayed relatively stable at the initial stages of the study, increased rapidly in mid-October, peaked in late-November, and plateaued in December. This trend agrees with the COVID-19 daily new confirmed case trend seen in Ohio (CDC, 2020a).

In general, wastewater from Jackson Pike and Southerly, the two Columbus WWTPs, showed 1-15 times higher viral concentrations than that from the other utilities in smaller cities (Fig. 2 ). By the end of 2020, Columbus had about 15-60 times more confirmed COVID-19 cases than the other 7 cities, while the cumulative case incidence was at the same magnitude among all the sites (5000-10,000 cases per million residents, Table 1). It is important to note that the variation of SARS-CoV-2 RNA concentration in wastewater among the sewersheds was not proportional to the variation in confirmed cases nor incidence. This finding suggests that wastewater is a complex matrix due to the variation in many factors, such as individual viral shedding amount and duration, RNA degradation rates, and migration of carriers. A previous study proposed an estimation of the prevalence of COVID-19 infection within a catchment from SARS-CoV-2 gene copies in wastewater (Ahmed et al., 2020a). Their model embedded other parameters of high uncertainty and variability, including flow rate and per capita production of wastewater, as well as viral shedding rate (Ahmed et al., 2020a). Despite these potential uncertainties, we postulate that WBE is still a powerful tool in capturing the real-time infection trend in communities.

Fig. 2.

Fig. 2

Longitudinal SARS-CoV-2 concentration trend in wastewater measured by N1, N2 and E genes from 9 wastewater catchments in Ohio in 2020.

3.3. Correlations between wastewater SARS-CoV-2 concentrations and COVID-19 cases

It is notable that the increased concentration of SARS-CoV-2 genes in wastewater during November and December 2020 coincided with the post-holiday COVID-19 surge, resulting from increased family gathering and travel. This result shows the usefulness of WBE in pinpointing epidemic hotspots (Hart and Halden, 2020). We hypothesized that the level of SARS-CoV-2 genes in wastewater correlate with the COVID-19 confirmed cases, so regression analyses were conducted for the nine sewersheds individually. As absolute case counts implicated the variation among the sites better than the incidences, absolute case numbers were employed in all the correlation tests in this study. Significant positive linear relationships were found between the wastewater SARS-CoV-2 concentrations and the case numbers reported on the sampling date for all the sites, except Athens (Pearson's correlation coefficients ranged from 0.38 to 0.89, Fig. S2h, Athens' data excluded from all correlation coefficients presented). Since both viral concentration and case data were highly skewed, violating the assumption of normality underlying the computation of the Pearson correlation coefficient (Fig. S1), the non-parametric Spearman rank correlation coefficients were also computed. The correlation coefficients of COVID-19 case counts and the three different SARS-CoV-2 gene concentrations were presented in a heatmap (Fig. 3c). The concentrations of all three SARS-CoV-2 genes were significantly, positively correlated with the daily confirmed cases for all sites, except Athens (Spearman's r ranged from 0.48 to 0.87, all p < 0.05), among which the N2 gene region achieved the best performance, indicated by its highest average Spearman rank correlation coefficients (Spearman's r = 0.70). The robustness of the N2 primer set in quantitative PCR is also shown in other studies, reporting that the primer binding region of the N2 gene region is less prone to mutation (Rahman et al., 2021). Therefore, the N2 gene region concentrations were used for further statistical analysis.

Fig. 3.

Fig. 3

Relationships between SARS-CoV-2 gene concentration in wastewater and new confirmed cases. Overlaid trend plots of SARS-CoV-2 N2 gene concentrations in wastewater and case number of different averaging methods in: a) Southerly sewershed population; b) Marietta sewershed population; c) Spearman correlations of all sites by different genes; and d) Spearman correlations of all sites by case number of different averaging methods. Significant correlations (Spearman) were highlighted with two asterisks and one asterisk for p-value < 0.05 and 0.05 < p-value < 0.1, respectively.

During an emerging epidemic, a time lag of 3-9 days is typically observed from the onset of symptoms to case reporting, depending on the testing capacity, testing method, care-seeking behavior, and reporting speed (Nemudryi et al., 2020; Garg et al., 2020; Silverman et al., 2020). In addition, the duration of viral shedding in human feces may vary among individuals (He et al., 2020; Xiao et al., 2020). To overcome these potential uncertainties, the case count obtained was based on the symptom onset date and the rolling averages of the confirmed new case data were calculated in replacement of the daily case numbers in this study. After averaging, the trend of case numbers was smoother and less noisy than the raw case numbers. This was observed in data from both big city, such as Southerly catchment of Columbus (Fig. 3a), and small cities like Marietta (Fig. 3b). Overlaid trend plots revealed good agreements between wastewater SARS-CoV-2 gene concentrations and new case numbers (Fig. S2a-S2g). Pearson (Fig. S2i) and Spearman (Fig. 3d) correlation coefficients both suggest that the averaged case numbers enhance the extent of relationships between the SARS-CoV-2 gene concentrations and reported COVID-19 cases. The sampling-date case number had the lowest coefficients among the four case types (averaged Spearman's r of all 9 sites = 0.70). The 5-day rolling average of case number showed the highest Spearman rank correlation coefficient (average Spearman's r = 0.77), followed by 7-day (averaged Spearman's r = 0.76) and 3-day averages (average Spearman's r = 0.75). As other studies pointed out that SARS-CoV-2 titers in wastewater may foreshadow the clinical results by 0-4 days, we staggered our WBE trend by 3 days, but found no improvement in the correlations (Nemudryi et al., 2020; Peccia et al., 2020; F. Wu A. Xiao J. Zhang K. Moniz N. Endo F. Armas R. Bonneau M.A. Brown M. Bushman P.R. Chai C. Duvallet T.B. Erickson K. Foppe N. Ghaeli X. Gu W.P. Hanage K.H. Huang W.L. Lee M. Matus K.A. McElroy J. Nagler S.F. Rhode M. Santillana J.A. Tucker S. Wuertz S. Zhao J. Thompson E.J. Alm, 2020). It is important to note that the Ohio positive cases are assigned a date of the estimate of disease onset, instead of the test date or the test result date. Considering both sensitivity and precision, the 5-day rolling average of the confirmed new cases was used for understanding the effectiveness of estimating COVID-19 prevalence from wastewater viral concentrations.

The only non-correlating community, Athens, is a small college town with students accounting for 80% population during a university semester. The confirmed case in Athens showed a different trend compared to other communities, with peak infection rates in mid-September and early October when students returned to campus, declined after that and much lower new case rate in November and December as students left campus by Thanksgiving holiday. Since most college students stay asymptomatic, the discrepancy between the wastewater data and new case data might be explained by an underestimation of the cases in the community, although more testing and analysis would have to be performed to confirm this hypothesis.

Among the nine sewersheds investigated, the wastewater data from four cities correlated remarkably well with the 5-day averaged new case numbers: Circleville WWTP (Spearman's r = 0.88), Newark WWTP (Spearman's r = 0.86), Marietta WWTP (Spearman's r = 0.85), and Jackson Pike WWTP (Spearman's r = 0.81). These findings demonstrate that the wastewater can be used to monitor the dynamic trend of COVID-19 disease in a community, regardless of the population size and magnitude of confirmed cases.

3.4. Estimation of COVID-19 cases via wastewater surveillance

Although WBE can provide unbiased samples of the community by aggregating population health information, wastewater is known to have relatively high day-to-day variation in sewage flow and fecal strength (J. Peccia A. Zulli D.E. Brackney, n.d.). To account for the varying estimated fecal load over time and possible dilution due to rain, two human-specific fecal viruses, PMMoV and crAssphage, were quantified from Columbus wastewater to normalize the SARS-CoV-2 concentrations. These two viruses have been used as an internal reference for method validation due to their high persistence in water compared to other bacterial fecal indicators (Greaves et al., 2020). Wastewater from the two Columbus sewersheds are a combined sewer (Table 1), which is more prone to dilution by stormwater events. For each sample analyzed, SARS-CoV-2 RNA concentrations were normalized with the concentrations of PMMoV (mean RNA concentration across the samples: ~1 × 106 gene copies/L of wastewater) and crAssphage (mean DNA concentration across the samples: ~1 × 108 gene copies/L of wastewater). Both normalization approaches improved the agreement of the viral concentration and the case counts visually, especially before the change of method (first month) (Fig. 4a). According to the Spearman rank correlation, the correlation between the viral titers and 5-day averaged case numbers was only marginally improved by the PMMoV-based normalization but not significant, whereas crAssphage-based normalization led to much weaker correlation.

Fig. 4.

Fig. 4

The effect of normalization with human fecal virus indicators on the relationships between SARS-CoV-2 N2 gene concentration in wastewater and 5-day-rolling averages of new confirmed cases. a) Overlaid trend plots of Southerly sewershed population; b) Linear regression model; and c) Quadratic polynomial model.

Our data showed that normalization did not significantly improve wastewater signal correlation with cases during the study period. Although our sites represent a mixture of facilities with separate and combined sewers, during the sampling period we only observed one to three instances per facility where the flows were significantly increased (doubled) compared to the lowest flow recorded during sampling. This primarily occurred in December due to snowmelt (peak of new cases per day), or in August during rain events (new cases close to zero). We ponder that these low frequency precipitation events did not affect the sewer system much, thus normalization of SARS-CoV-2 gene concentrations with human fecal strength did not improve the correlations. In this regard, assumptions can be made that longitudinal wastewater data is robust to the variations in sewage flow and fecal strength when extreme precipitation events are infrequent. Our results agreed with the findings from other studies, which concluded that the PMMoV-normalized SARS-CoV-2 signal had lower background noise and showed the strongest correlation with active cases (F. Wu A. Xiao J. Zhang K. Moniz N. Endo F. Armas R. Bonneau M.A. Brown M. Bushman P.R. Chai C. Duvallet T.B. Erickson K. Foppe N. Ghaeli X. Gu W.P. Hanage K.H. Huang W.L. Lee M. Matus K.A. McElroy J. Nagler S.F. Rhode M. Santillana J.A. Tucker S. Wuertz S. Zhao J. Thompson E.J. Alm, 2020; D'Aoust et al., 2021). For future studies where normalization is required, combined markers of viral indicators, solid contents, and other volumetric parameters are recommended (Neault et al., 2020).

While clinical test results tend to be highly delayed and underestimated, wastewater enables the temporal mapping of the outbreak in a more timely and accurate manner (Garg et al., 2020). As more and more efforts are put into wastewater surveillance, population health data from wastewater is accumulating worldwide. To make better use of these wastewater information, we tested different models to help estimate COVID-19 prevalence from wastewater viral loads. First, a linear model was built (R 2 based on raw N2 gene region concentration in Southerly wastewater and 5-day averaged case number = 0.84). Surprisingly, neither normalization approaches enhanced the model (Fig. 4b). As mentioned prior, the linear model is not ideal for our dataset and data transformation hardly improved the normality. For a better estimation, polynomial models were built and evaluated. Both quadratic and cubic polynomial models achieved higher R 2 than the corresponding linear model. Using the Southerly data as an example, R 2 of 0.88 and 0.89, respectively were achieved (Fig. 4c). The polynomial models also showed better adherence to normality. However, regression analysis indicated that the cubic polynomial model is not significantly superior to the quadratic model (p < 0.05). Based on these results, it can be concluded that the quadratic model gave the best description of the relationship of new COVID-19 cases and viral titers in wastewater, while minimizing overfitting and the violation of normality. Similar to the case in the linear model, normalization did not improve the quadratic model (Fig. 4c).

These results demonstrate that dynamic trend of COVID-19 within a community can be well estimated from longitudinal SARS-CoV-2 gene concentrations in wastewater. Polynomial models were built and optimized for the wastewater data from eight of the nine sewersheds. It has been reported that the viral titer in wastewater is more associated with the demographic variables, the household income and medical spend for example, than with population size (F. Wu A. Xiao J. Zhang K. Moniz N. Endo F. Armas R. Bonneau M.A. Brown M. Bushman P.R. Chai C. Duvallet T.B. Erickson K. Foppe N. Ghaeli X. Gu W.P. Hanage K.H. Huang W.L. Lee M. Matus K.A. McElroy J. Nagler S.F. Rhode M. Santillana J.A. Tucker S. Wuertz S. Zhao J. Thompson E.J. Alm, 2020). This may help explain the failure of estimating the disease prevalence with WBE data from Athens. For low-income areas with limited testing capability, it is recommended to take more demographic variables into account when using the WBE as a surveillance tool for the pandemic. Furthermore, recent studies and our preliminary data generated at the early stage of the pandemic (March to May; data now shown) suggested that WBE can be applied to communities of low prevalence (Randazzo et al., 2020). As new confirmed cases have been decreasing worldwide due to the implementation of vaccinations, more sensitive and robust methods will perform better in determining SARS-CoV-2 genetic signals in wastewater in the areas with lower COVID-19 prevalence than before.

3.5. SARS-CoV-2 variant identification in wastewater

Sequencing of the entire SARS-CoV-2 genome was performed on a subset of wastewater samples. Sequencing results differed among the 8 sites where wastewater samples were obtained over a 3-day period in early January 2021 (Table 2 ). The Spike (S) D614G variant has dominated the global pandemic since March 2020, showing increased infectivity and viral shedding (Korber et al., 2020), and all wastewater samples showed nearly 100% D614G. However, there were variations in the levels of some other single nucleotide variants associated with common US-based clades from this time period including 20C/G (bearing ORF3A Q57H), 20B (N R203K), and 20A (N S194L), with a predominance of clade 20C variants in most samples. Detected SARS-CoV-2 variants in wastewater agreed well with the sequencing surveillance performed on SARS-CoV-2-positive nasal swabs (Table 2). For example, during January 2021, S N501Y-bearing 20G virus (Tu et al., 2021) and the B.1.1.429 strain also bearing N501Y (CDC, 2020b) were first detected in a few Columbus Ohio patients and seen at 8% variant fraction in the Columbus Jackson Pike sewershed samples (Table 2). In addition, there were low levels of other variants associated with strains that were first detected in patients from Central and Southern Ohio during late 2020/early 2021, including S L452R (associated with the B.1.427/429 strains), found at 10% variant fraction in Zanesville and 7% in Marietta wastewater samples. This was important information since multiple studies during this period reported increased infectivity and transmissibility as well as decreased antibody neutralization for viruses carrying S L452R and/or S N501Y mutations compared to the D614G alone (Deng et al., 2021; Xie et al., 2021). It is notable that wastewater samples from different sewersheds (Jackson Pike and Southerly) in the same city (Columbus) showed distinct variant patterns which could have reflected local differences during this period of high strain diversity in patients. The limited data in this study thus provides support for the feasibility of identifying low-levels of strain-defining variants indicative of emerging circulating SARS-CoV-2 strains in various communities from wastewater.

Table 2.

Differential detection of SARS-CoV-2 strain-defining mutations by genomic sequencing in wastewater across Ohio over a 3-day period in early January 2021.

Amino acid change Nucleotide change Strain/lineage with mutation Detection frequency in NP swabsc Variant fraction
Marysville Jackson Pike Southerly Athens Marietta Zanesville Circleville Lancaster
S: D614Ga c.1841A > G B.1, clades A,B,C 100% 0.97 0.97 0.98 0.95 0.95 0.96 0.98 0.97
ORF3A: Q57Hb c.171G > T B.1, 20C/G clade 95% 0.88 0.73 0.80 0.43 0.91 0.89 0.77 0.80
N: R203K c.608G > A B.1, 20B clade 3% nd nd nd 0.19 nd nd nd nd
N: S194L c.581C > T B.1, 20A clade 2% nd nd nd 0.24 nd nd 0.14 0.07
S: N501Y c.1501A > T B.1.2/501Y 4% nd 0.08 nd nd nd nd nd nd
S: S477N c.1430G > A B.1.1.298 & B.1.404 <1% nd nd 0.16 nd nd nd 0.08 nd
S: L452R c.1355 T > G B.1.1.427 & B.1.1.429 1% nd nd 0.06 nd 0.07 0.10 nd nd
S: P681H c.2042C > A B.1.1.222 & B.1.1.7 3% nd nd 0.09 nd nd nd 0.18 nd
N: Q9H c.27G > T B.1, 20C subset 4% nd 0.14 nd 0.14 0.08 0.07 nd nd
a

Variant fraction was well-correlated with other B.1 markers including the 5′UTR C241T, nsp3 p.F106F (c.318C > T) and nsp12 p.P323L (c.968C > T).

b

Variant fraction was well-correlated with clade 20C/G marker nsp2 p.T85I (c.254C > T).

c

SARS-CoV-2-positive nasal or nasopharyngeal (NP) swabs collected in January 2021.

3.6. Significance of this work

This study demonstrates the effectiveness of wastewater surveillance in COVID-19 trend tracking in various communities. SARS-CoV-2 gene concentrations in wastewater strongly correlated with the COVID-19 cases. This is the first study proposing the use of a quadratic polynomial model to track COVID-19 cases from wastewater surveillance data, which can benefit the communities with limited human testing capability. In the later stage of the pandemic, WBE can help evaluate the effectiveness of vaccination and prioritize the distribution of human testing resources. Moreover, as sequencing results from wastewater samples in early 2021 at a time of new strain emergence shows an agreement with the sequencing results from clinical nasal swab samples, we suggest that the wastewater matrix is an ideal sample for fast tracking variant emergence and transmission within a community.

CRediT authorship contribution statement

Yuehan Ai: Methodology, Data curation, Formal analysis, Investigation, Visualization, Writing – original draft. Angela Davis: Methodology, Investigation, Validation, Writing – review & editing. Dan Jones: Funding acquisition, Supervision, Writing – review & editing. Stanley Lemeshow: Funding acquisition, Methodology, Writing – review & editing. Huolin Tu: Methodology, Investigation, Writing – review & editing. Fan He: Investigation. Peng Ru: Investigation. Xiaokang Pan: Investigation. Zuzana Bohrerova: Funding acquisition, Project administration, Writing – review & editing. Jiyoung Lee: Conceptualization, Funding acquisition, Methodology, Investigation, Project administration, Resources, Supervision, Writing – review & editing.

Declaration of competing interest

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Acknowledgments

This study was supported by funding from Ohio Environmental Protection Agency's Coronavirus Aid, Relief, and Economic Security (CARES) Act (JL, ZB, SL) and an Interdisciplinary Research Seed Grant from The Ohio State University Infectious Diseases Institute (DJ, HT, JL). Genomic surveillance of nasal swabs was performed under an IRB-approved surveillance protocol (DJ). This research could not be completed without the collaboration with participating wastewater treatment plants in Ohio. We thank Pam Snyder, Sarah Corcoran, and Charlie Andorka at The Ohio State University for their assistance in sample processing and collection and Preeti Pancholi, Sara Koenig and Peter Mohler for logistical support. We appreciate the great support from Rebecca Fugitt at Ohio Department of Health during this study.

Editor: Frederic Coulon

Footnotes

Appendix A

Supplementary data to this article can be found online at https://doi.org/10.1016/j.scitotenv.2021.149757.

Appendix A. Supplementary data

Supplementary material

mmc1.docx (924.3KB, docx)

References

  1. Ahmed W., Angel N., Edson J., Bibby K., Bivins A., O’Brien J.W., Choi P.M., Kitajima M., Simpson S.L., Li J., Tscharke B., Verhagen R., Smith W.J.M., Zaugg J., Dierens L., Hugenholtz P., Thomas K.V., Mueller J.F. First confirmed detection of SARS-CoV-2 in untreated wastewater in Australia: a proof of concept for the wastewater surveillance of COVID-19 in the community. Sci. Total Environ. 2020;728 doi: 10.1016/j.scitotenv.2020.138764. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Ahmed W., Bertsch P.M., Bivins A., Bibby K., Farkas K., Gathercole A., Haramoto E., Gyawali P., Korajkic A., McMinn B.R., Mueller J.F., Simpson S.L., Smith W.J.M., Symonds E.M., Thomas K.V., Verhagen R., Kitajima M. Comparison of virus concentration methods for the RT-qPCR-based recovery of murine hepatitis virus, a surrogate for SARS-CoV-2 from untreated wastewater. Sci. Total Environ. 2020;739 doi: 10.1016/j.scitotenv.2020.139960. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Ahmed W., Tscharke B., Bertsch P.M., Bibby K., Bivins A., Choi P., Clarke L., Dwyer J., Edson J., Nguyen T.M.H., O’Brien J.W., Simpson S.L., Sherman P., Thomas K.V., Verhagen R., Zaugg J., Mueller J.F. SARS-CoV-2 RNA monitoring in wastewater as a potential early warning system for COVID-19 transmission in the community: a temporal case study. Sci. Total Environ. 2021;761 doi: 10.1016/j.scitotenv.2020.144216. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bae J., Schwab K.J. Evaluation of murine norovirus, feline calicivirus, poliovirus, and MS2 as surrogates for human norovirus in a model of viral persistence in surface water and groundwater. Appl. Environ. Microbiol. 2008;74:477–484. doi: 10.1128/AEM.02095-06. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Bennett H.B., O’Dell H.D., Norton G., Shin G., Hsu F.-C., Meschke J.S. Evaluation of a novel electropositive filter for the concentration of viruses from diverse water matrices. Water Sci. Technol. J. Int. Assoc. Water Pollut. Res. 2010;61:317–322. doi: 10.2166/wst.2010.819. [DOI] [PubMed] [Google Scholar]
  6. CDC, 2020a. COVID data tracker [online]. Cent. Dis. Control Prev. URL https://covid.cdc.gov/covid-data-tracker (accessed 3.10.21).
  7. CDC, 2020b. Cases, data, and surveillance [online]. Cent. Dis. Control Prev. URL https://www.cdc.gov/coronavirus/2019-ncov/cases-updates/variant-surveillance/variant-info.html (accessed 3.29.21).
  8. Cheung K.S., Hung I.F.N., Chan P.P.Y., Lung K.C., Tso E., Liu R., Ng Y.Y., Chu M.Y., Chung T.W.H., Tam A.R., Yip C.C.Y., Leung K.-H., Fung A.Y.-F., Zhang R.R., Lin Y., Cheng H.M., Zhang A.J.X., To K.K.W., Chan K.-H., Yuen K.-Y., Leung W.K. Gastrointestinal manifestations of SARS-CoV-2 infection and virus load in fecal samples from a Hong Kong cohort: systematic review and meta-analysis. Gastroenterology. 2020;159:81–95. doi: 10.1053/j.gastro.2020.03.065. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Cimolai N. Environmental and decontamination issues for human coronaviruses and their potential surrogates. J. Med. Virol. 2020;92:2498–2510. doi: 10.1002/jmv.26170. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Consortium, S.-C.-2 I. Pecson B.M., Darby E., Haas C.N., Amha Y.M., Bartolo M., Danielson R., Dearborn Y., Giovanni G.D., Ferguson C., Fevig S., Gaddis E., Gray D., Lukasik G., Mull B., Olivas L., Olivieri A., Qu Y. Reproducibility and sensitivity of 36 methods to quantify the SARS-CoV-2 genetic signal in raw wastewater: findings from an interlaboratory methods evaluation in the U.S. Environ. Sci. Water Res. Technol. 2021 doi: 10.1039/D0EW00946F. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Corman V.M., Landt O., Kaiser M., Molenkamp R., Meijer A., Chu D.K., Bleicker T., Brünink S., Schneider J., Schmidt M.L., Mulders D.G., Haagmans B.L., van der Veer B., van den Brink S., Wijsman L., Goderski G., Romette J.-L., Ellis J., Zambon M., Peiris M., Goossens H., Reusken C., Koopmans M.P., Drosten C. Detection of 2019 novel coronavirus (2019-nCoV) by real-time RT-PCR. Eurosurveillance. 2020;25:2000045. doi: 10.2807/1560-7917.ES.2020.25.3.2000045. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. D’Aoust P.M., Mercier E., Montpetit D., Jia J.-J., Alexandrov I., Neault N., Baig A.T., Mayne J., Zhang X., Alain T., Langlois M.-A., Servos M.R., MacKenzie M., Figeys D., MacKenzie A.E., Graber T.E., Delatolla R. Quantitative analysis of SARS-CoV-2 RNA from wastewater solids in communities with low COVID-19 incidence and prevalence. Water Res. 2021;188 doi: 10.1016/j.watres.2020.116560. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Dare R.K., Fry A.M., Chittaganpitch M., Sawanpanyalert P., Olsen S.J., Erdman D.D. Human coronavirus infections in rural Thailand: a comprehensive study using real-time reverse-transcription polymerase chain reaction assays. J. Infect. Dis. 2007;196:1321–1328. doi: 10.1086/521308. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Daughton C.G. Using biomarkers in sewage to monitor community-wide human health: isoprostanes as conceptual prototype. Sci. Total Environ. 2012;424:16–38. doi: 10.1016/j.scitotenv.2012.02.038. [DOI] [PubMed] [Google Scholar]
  15. Dawson D.J., Paish A., Staffell L.M., Seymour I.J., Appleton H. Survival of viruses on fresh produce, using MS2 as a surrogate for norovirus. J. Appl. Microbiol. 2005;98:203–209. doi: 10.1111/j.1365-2672.2004.02439.x. [DOI] [PubMed] [Google Scholar]
  16. Decaro N., Elia G., Campolo M., Desario C., Mari V., Radogna A., Colaianni M.L., Cirone F., Tempesta M., Buonavoglia C. Detection of bovine coronavirus using a TaqMan-based real-time RT-PCR assay. J. Virol. Methods. 2008;151:167–171. doi: 10.1016/j.jviromet.2008.05.016. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Deng X., Garcia-Knight M.A., Khalid M.M., Servellita V., Wang C., Morris M.K., Sotomayor-González A., Glasner D.R., Reyes K.R., Gliwa A.S., Reddy N.P., Martin C.S.S., Federman S., Cheng J., Balcerek J., Taylor J., Streithorst J.A., Miller S., Kumar G.R., Sreekumar B., Chen P.-Y., Schulze-Gahmen U., Taha T.Y., Hayashi J., Simoneau C.R., McMahon S., Lidsky P.V., Xiao Y., Hemarajata P., Green N.M., Espinosa A., Kath C., Haw M., Bell J., Hacker J.K., Hanson C., Wadford D.A., Anaya C., Ferguson D., Lareau L.F., Frankino P.A., Shivram H., Wyman S.K., Ott M., Andino R., Chiu C.Y. 2021. Transmission, Infectivity, and Antibody Neutralization of an Emerging SARS-CoV-2 Variant in California Carrying a L452R Spike Protein Mutation. medRxiv 2021.03.07.21252647. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. F. Wu A. Xiao J. Zhang K. Moniz N. Endo F. Armas R. Bonneau M.A. Brown M. Bushman P.R. Chai C. Duvallet T.B. Erickson K. Foppe N. Ghaeli X. Gu W.P. Hanage K.H. Huang W.L. Lee M. Matus K.A. McElroy J. Nagler S.F. Rhode M. Santillana J.A. Tucker S. Wuertz S. Zhao J. Thompson E.J. Alm , 2020a. SARS-CoV-2 Titers in Wastewater Foreshadow Dynamics and Clinical Presentation of New COVID-19 Cases. medRxiv. doi:10.1101/2020.06.15.20117747
  19. F. Wu J. Zhang A. Xiao X. Gu W.L. Lee F. Armas K. Kauffman W. Hanage M. Matus N. Ghaeli N. Endo C. Duvallet M. Poyet K. Moniz A.D. Washburne T.B. Erickson P.R. Chai J. Thompson E.J. Alm , 2020b. SARS-CoV-2 titers in wastewater are higher than expected from clinically confirmed cases. mSystems 5. doi:10.1128/mSystems.00614-20 [DOI] [PMC free article] [PubMed]
  20. Fontenele R.S., Kraberger S., Hadfield J., Driver E.M., Bowes D., Holland L.A., Faleye T.O.C., Adhikari S., Kumar R., Inchausti R., Holmes W.K., Deitrick S., Brown P., Duty D., Smith T., Bhatnagar A., Yeager R.A., Holm R.H., Reitzenstein N.H.von, Wheeler E., Dixon K., Constantine T., Wilson M.A., Lim E.S., Jiang X., Halden R.U., Scotch M., Varsani A. 2021. High-throughput Sequencing of SARS-CoV-2 in Wastewater Provides Insights Into Circulating Variants. medRxiv 2021.01.22.21250320. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. G.L. Rosa M. Iaconelli P. Mancini G.B. Ferraro L. Bonadonna L. Lucentini E Suffredini ., n.d. First Detection of SARS-COV-2 in Untreated Wastewaters in Italy 17. [DOI] [PMC free article] [PubMed]
  22. Garg S., Kim L., Whitaker M., O’Halloran A., Cummings C., Holstein R., Prill M., Chai S.J., Kirley P.D., Alden N.B., Kawasaki B., Yousey-Hindes K., Niccolai L., Anderson E.J., Openo K.P., Weigel A., Monroe M.L., Ryan P., Henderson J., Kim S., Como-Sabetti K., Lynfield R., Sosin D., Torres S., Muse A., Bennett N.M., Billing L., Sutton M., West N., Schaffner W., Talbot H.K., Aquino C., George A., Budd A., Brammer L., Langley G., Hall A.J., Fry A. Hospitalization rates and characteristics of patients hospitalized with laboratory-confirmed coronavirus disease 2019 — COVID-NET, 14 states, march 1–30, 2020. Morb. Mortal. Wkly Rep. 2020;69:458–464. doi: 10.15585/mmwr.mm6915e3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Greaves J., Stone D., Wu Z., Bibby K. Persistence of emerging viral fecal indicators in large-scale freshwater mesocosms. Water Res. X. 2020;9 doi: 10.1016/j.wroa.2020.100067. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Hamza I.A., Jurzik L., Überla K., Wilhelm M. Evaluation of pepper mild mottle virus, human picobirnavirus and torque Teno virus as indicators of fecal contamination in river water. Water Res. 2011;45:1358–1368. doi: 10.1016/j.watres.2010.10.021. [DOI] [PubMed] [Google Scholar]
  25. Haramoto E., Kitajima M., Kishida N., Konno Y., Katayama H., Asami M., Akiba M. Occurrence of pepper mild mottle virus in drinking water sources in Japan. Appl. Environ. Microbiol. 2013;79:7413–7418. doi: 10.1128/AEM.02354-13. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Hart O.E., Halden R.U. Computational analysis of SARS-CoV-2/COVID-19 surveillance by wastewater-based epidemiology locally and globally: feasibility, economy, opportunities and challenges. Sci. Total Environ. 2020;730 doi: 10.1016/j.scitotenv.2020.138875. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. He X., Lau E.H.Y., Wu P., Deng X., Wang J., Hao X., Lau Y.C., Wong J.Y., Guan Y., Tan X., Mo X., Chen Y., Liao B., Chen W., Hu F., Zhang Q., Zhong M., Wu Y., Zhao L., Zhang F., Cowling B.J., Li F., Leung G.M. Temporal dynamics in viral shedding and transmissibility of COVID-19. Nat. Med. 2020;26:672–675. doi: 10.1038/s41591-020-0869-5. [DOI] [PubMed] [Google Scholar]
  28. Hirotsu Y., Mochizuki H., Omata M. 2020. Double-Quencher Probes Improved the Detection Sensitivity of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) by One-Step RT-PCR. medRxiv 2020.03.17.20037903. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Hu B., Guo H., Zhou P., Shi Z.-L. Characteristics of SARS-CoV-2 and COVID-19. Nat. Rev. Microbiol. 2021;19:141–154. doi: 10.1038/s41579-020-00459-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Innovaprep . Concentrating Pipette Select: Wastewater Application Note Revision B. 2020. p. 2.https://uploads-ssl.webflow.com/57aa3257c3e841c509f276e2/5f888d1b3bddf35ae661965c_CONCENTRATINGPIPETTESELECT%20WASTEWATER%20APPLICATION%20NOTE%201.17.03%20PM-compressed.pdf [Online]. URL. (accessed 3.3.21) [Google Scholar]
  31. J. Peccia A. Zulli D.E. Brackney N.D. Grubaugh E.H. Kaplan A. Casanovas-Massana A.I. Ko A.A. Malik D. Wang M. Wang J.L. Warren D.M. Weinberger S.B. Omer , 2020b. SARS-CoV-2 RNA Concentrations in Primary Municipal Sewage Sludge as a Leading Indicator of COVID-19 Outbreak Dynamics. medRxiv 2020.05.19.20105999. doi:10.1101/2020.05.19.20105999
  32. Jahn K., Dreifuss D., Topolsky I., Kull A., Ganesanandamoorthy P., Fernandez-Cassi X., Bänziger C., Stachler E., Fuhrmann L., Jablonski K.P., Chen C., Aquino C., Stadler T., Ort C., Kohn T., Julian T.R., Beerenwinkel N. 2021. Detection of SARS-CoV-2 Variants in Switzerland by Genomic Analysis of Wastewater Samples. medRxiv 2021.01.08.21249379. [DOI] [Google Scholar]
  33. Johnson D.R., Lee P.K.H., Holmes V.F., Alvarez-Cohen L. An internal reference technique for accurately quantifying specific mRNAs by real-time PCR with application to the tceA reductive dehalogenase gene. Appl. Environ. Microbiol. 2005;71:3866–3871. doi: 10.1128/AEM.71.7.3866-3871.2005. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Jung Y.J., Park G.-S., Moon J.H., Ku K., Beak S.-H., Kim S., Park E.C., Park D., Lee J.-H., Byeon C.W., Lee J.J., Maeng J.-S., Kim S.J., Kim S.I., Kim B.-T., Lee M.J., Kim H.G. 2020. Comparative Analysis of Primer-probe Sets for the Laboratory Confirmation of SARS-CoV-2. bioRxiv 2020.02.25.964775. [DOI] [PubMed] [Google Scholar]
  35. L. Kevin , 2020. Back log of test results causes delayed COVID-19 numbers reported by ODH [Online]. URL https://www.10tv.com/article/news/health/coronavirus/back-log-of-test-results-causes-delayed-covid-19-numbers-reported-by-odh/530-2e377780-687b-4ee2-b7fb-8f9991bb15d0 (accessed 3.11.21).
  36. Korber B., Fischer W.M., Gnanakaran S., Yoon H., Theiler J., Abfalterer W., Hengartner N., Giorgi E.E., Bhattacharya T., Foley B., Hastie K.M., Parker M.D., Partridge D.G., Evans C.M., Freeman T.M., de Silva T.I., Angyal A., Brown R.L., Carrilero L., Green L.R., Groves D.C., Johnson K.J., Keeley A.J., Lindsey B.B., Parsons P.J., Raza M., Rowland-Jones S., Smith N., Tucker R.M., Wang D., Wyles M.D., McDanal C., Perez L.G., Tang H., Moon-Walker A., Whelan S.P., LaBranche C.C., Saphire E.O., Montefiori D.C. Tracking changes in SARS-CoV-2 spike: evidence that D614G increases infectivity of the COVID-19 virus. Cell. 2020;182:812–827.e19. doi: 10.1016/j.cell.2020.06.043. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Lin K., Marr L.C. Aerosolization of ebola virus surrogates in wastewater systems. Environ. Sci. Technol. 2017;51:2669–2675. doi: 10.1021/acs.est.6b04846. [DOI] [PubMed] [Google Scholar]
  38. Liu J., Liao X., Qian S., Yuan J., Wang F., Liu Y., Wang Z., Wang F.-S., Liu L., Zhang Z. Community transmission of severe acute respiratory syndrome coronavirus 2, Shenzhen, China, 2020. Emerg. Infect. Dis. 2020;26:1320–1323. doi: 10.3201/eid2606.200239. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Lodder W., Husman A.M.de R. SARS-CoV-2 in wastewater: potential health risk, but also data source. Lancet Gastroenterol. Hepatol. 2020;5:533–534. doi: 10.1016/S2468-1253(20)30087-X. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Malla B., Ghaju Shrestha R., Tandukar S., Sherchand J.B., Haramoto E. Performance evaluation of human-specific viral markers and application of pepper mild mottle virus and crassphage to environmental water samples as fecal pollution markers in the Kathmandu Valley, Nepal. Food Environ. Virol. 2019;11:274–287. doi: 10.1007/s12560-019-09389-x. [DOI] [PubMed] [Google Scholar]
  41. Martin J., Klapsa D., Wilton T., Zambon M., Bentley E., Bujaki E., Fritzsche M., Mate R., Majumdar M. Tracking SARS-CoV-2 in sewage: evidence of changes in virus variant predominance during COVID-19 pandemic. Viruses. 2020;12:1144. doi: 10.3390/v12101144. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Medema G., Heijnen L., Elsinga G., Italiaander R., Brouwer A. Presence of SARS-Coronavirus-2 in sewage (preprint) Occup. Environ. Health. 2020 doi: 10.1101/2020.03.29.20045880. [DOI] [PubMed] [Google Scholar]
  43. Neault N., Baig A.T., Graber T.E., D’Aoust P.M., Mercier E., Alexandrov I., Crosby D., Baird S., Mayne J., Pounds T., MacKenzie M., Figeys D., MacKenzie A., Delatolla R. 2020. SARS-CoV-2 Protein in Wastewater Mirrors COVID-19 Prevalence. medRxiv 2020.09.01.20185280. [DOI] [Google Scholar]
  44. Nemudryi A., Nemudraia A., Wiegand T., Surya K., Buyukyoruk M., Cicha C., Vanderwood K.K., Wilkinson R., Wiedenheft B. Temporal detection and phylogenetic assessment of SARS-CoV-2 in municipal wastewater. Cell Rep. Med. 2020;1 doi: 10.1016/j.xcrm.2020.100098. [DOI] [PMC free article] [PubMed] [Google Scholar]
  45. Odh COVID-19 dashborad: Ohio coronavirus wastewater monitoring network [Online] 2021. https://public.tableau.com/views/COVIDWastewater/Dashboard2?:embed=y&:showVizHome=no&:host_url=https%3A%2F%2Fpublic.tableau.com%2F&:embed_code_version=3&:tabs=no&:toolbar=yes&:display_count=yes&:language=en&:loadOrderID=0
  46. Ogorzaly L., Gantzer C. Development of real-time RT-PCR methods for specific detection of F-specific RNA bacteriophage genogroups: application to urban raw wastewater. J. Virol. Methods. 2006;138:131–139. doi: 10.1016/j.jviromet.2006.08.004. [DOI] [PubMed] [Google Scholar]
  47. Peccia J., Zulli A., Brackney D.E., Grubaugh N.D., Kaplan E.H., Casanovas-Massana A., Ko A.I., Malik A.A., Wang D., Wang M., Warren J.L., Weinberger D.M., Arnold W., Omer S.B. Measurement of SARS-CoV-2 RNA in wastewater tracks community infection dynamics. Nat. Biotechnol. 2020;38:1164–1167. doi: 10.1038/s41587-020-0684-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
  48. Rahman M.S., Islam M.R., Alam A.S.M.R.U., Islam I., Hoque M.N., Akter S., Rahaman M.M., Sultana M., Hossain M.A. Evolutionary dynamics of SARS-CoV-2 nucleocapsid protein and its consequences. J. Med. Virol. 2021;93:2177–2195. doi: 10.1002/jmv.26626. [DOI] [PubMed] [Google Scholar]
  49. Rambaut A., Holmes E.C., O’Toole Á., Hill V., McCrone J.T., Ruis C., du Plessis L., Pybus O.G. A dynamic nomenclature proposal for SARS-CoV-2 lineages to assist genomic epidemiology. Nat. Microbiol. 2020;5:1403–1407. doi: 10.1038/s41564-020-0770-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  50. Randazzo W., Truchado P., Cuevas-Ferrando E., Simón P., Allende A., Sánchez G. SARS-CoV-2 RNA in wastewater anticipated COVID-19 occurrence in a low prevalence area. Water Res. 2020;181 doi: 10.1016/j.watres.2020.115942. [DOI] [PMC free article] [PubMed] [Google Scholar]
  51. Richterich P. Infectious Diseases (Except HIV/AIDS) 2020. Severe underestimation of COVID-19 case numbers: effect of epidemic growth rate and test restrictions (preprint) [DOI] [Google Scholar]
  52. Sedlak R.H., Kuypers J., Jerome K.R. A multiplexed droplet digital PCR assay performs better than qPCR on inhibition prone samples. Diagn. Microbiol. Infect. Dis. 2014;80:285–286. doi: 10.1016/j.diagmicrobio.2014.09.004. [DOI] [PubMed] [Google Scholar]
  53. Silverman J.D., Hupert N., Washburne A.D. Using influenza surveillance networks to estimate state-specific prevalence of SARS-CoV-2 in the United States. Sci. Transl. Med. 2020;12 doi: 10.1126/scitranslmed.abc1126. [DOI] [PMC free article] [PubMed] [Google Scholar]
  54. Sims N., Kasprzyk-Hordern B. Future perspectives of wastewater-based epidemiology: monitoring infectious disease spread and resistance to the community level. Environ. Int. 2020;139 doi: 10.1016/j.envint.2020.105689. [DOI] [PMC free article] [PubMed] [Google Scholar]
  55. Stachler E., Kelty C., Sivaganesan M., Li X., Bibby K., Shanks O.C. Quantitative CrAssphage PCR assays for human fecal pollution measurement. Environ. Sci. Technol. 2017;51:9146–9154. doi: 10.1021/acs.est.7b02703. [DOI] [PMC free article] [PubMed] [Google Scholar]
  56. Symonds E.M., Nguyen K.H., Harwood V.J., Breitbart M. Pepper mild mottle virus: a plant pathogen with a greater purpose in (waste)water treatment development and public health management. Water Res. 2018;144:1–12. doi: 10.1016/j.watres.2018.06.066. [DOI] [PMC free article] [PubMed] [Google Scholar]
  57. T. Bedford E. Hodcroft R. Neher , n.d. Updated Nextstrain SARS-CoV-2 Clade Naming Strategy [Online]. Updat. Nextstrain SARS-CoV-2 Clade Naming Strategy. URL https://nextstrain.org//blog/2021-01-06-updated-SARS-CoV-2-clade-naming (accessed 4.14.21).
  58. Tu H., Avenarius M.R., Kubatko L., Hunt M., Pan X., Ru P., Garee J., Thomas K., Mohler P., Pancholi P., Jones D. 2021. Distinct Patterns of Emergence of SARS-CoV-2 Spike Variants Including N501Y in Clinical Samples in Columbus Ohio. bioRxiv 2021.01.12.426407. [DOI] [Google Scholar]
  59. U.S. Department of Commerce U.S. Census Bureau QuickFacts: United States [online] 2019. https://www.census.gov/quickfacts/fact/table/US/PST045219 URL. (accessed 3.9.21)
  60. Wang X., Zheng J., Guo L., Yao H., Wang L., Xia X., Zhang W. Fecal viral shedding in COVID-19 patients: clinical significance, viral load dynamics and survival analysis. Virus Res. 2020;289 doi: 10.1016/j.virusres.2020.198147. [DOI] [PMC free article] [PubMed] [Google Scholar]
  61. World Health Organization (WHO) WHO coronavirus disease (COVID-19) dashboard [online] 2021. https://covid19.who.int URL. (accessed 3.3.21)
  62. Wurtzer S., Marechal V., Mouchel J., Maday Y., Teyssou R., Richard E., Almayrac J., Moulin L. Evaluation of lockdown impact on SARS-CoV-2 dynamics through viral genome quantification in Paris wastewaters (preprint) Epidemiology. 2020 doi: 10.1101/2020.04.12.20062679. [DOI] [PMC free article] [PubMed] [Google Scholar]
  63. Xiao F., Tang M., Zheng X., Liu Y., Li X., Shan H. Evidence for gastrointestinal infection of SARS-CoV-2. Gastroenterology. 2020;158:1831–1833.e3. doi: 10.1053/j.gastro.2020.02.055. [DOI] [PMC free article] [PubMed] [Google Scholar]
  64. Xie X., Liu Y., Liu J., Zhang X., Zou J., Fontes-Garfias C.R., Xia H., Swanson K.A., Cutler M., Cooper D., Menachery V.D., Weaver S.C., Dormitzer P.R., Shi P.-Y. Neutralization of SARS-CoV-2 spike 69/70 deletion, E484K and N501Y variants by BNT162b2 vaccine-elicited sera. Nat. Med. 2021;1–2 doi: 10.1038/s41591-021-01270-4. [DOI] [PubMed] [Google Scholar]
  65. Ye Y., Ellenberg R.M., Graham K.E., Wigginton K.R. Survivability, partitioning, and recovery of enveloped viruses in untreated municipal wastewater. Environ. Sci. Technol. 2016;50:5077–5085. doi: 10.1021/acs.est.6b00876. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Supplementary material

mmc1.docx (924.3KB, docx)

Articles from The Science of the Total Environment are provided here courtesy of Elsevier

RESOURCES