Tools for interpretation of wastewater SARS-CoV-2 temporal and spatial trends demonstrated with data collected in the San Francisco Bay Area

Hannah Greenwald(University of California, Berkeley), Lauren C. Kennedy(University of California, Berkeley), Adrian Hinkle(University of California, Berkeley), Oscar N. Whitney(University of California, Berkeley), Vinson B. Fan(University of California, Berkeley), Alexander Crits‐Christoph(Innovative Genomics Institute), Sasha Harris-Lovett(University of California, Berkeley), Avi I. Flamholz(California Institute of Technology), Basem Al-Shayeb(Innovative Genomics Institute), Lauren D. Liao(University of California, Berkeley), Matt Beyers(Alameda County Public Health Department), Daniel B. Brown(Contra Costa Health Services), Alicia R. Chakrabarti, Jason Dow(Zero Breast Cancer), Dan Frost, Mark Koekemoer(Zero Breast Cancer), Chris Lynch(Contra Costa Health Services), Payal Sarkar(Santa Clara County Behavioral Health Services), Eileen White, Rose S. Kantor(University of California, Berkeley), Kara L. Nelson(Innovative Genomics Institute)
Water Research X
July 31, 2021
Cited by 123Open Access
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Abstract

Wastewater surveillance for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) RNA can be integrated with COVID-19 case data to inform timely pandemic response. However, more research is needed to apply and develop systematic methods to interpret the true SARS-CoV-2 signal from noise introduced in wastewater samples (e.g., from sewer conditions, sampling and extraction methods, etc.). In this study, raw wastewater was collected weekly from five sewersheds and one residential facility. The concentrations of SARS-CoV-2 in wastewater samples were compared to geocoded COVID-19 clinical testing data. SARS-CoV-2 was reliably detected (95% positivity) in frozen wastewater samples when reported daily new COVID-19 cases were 2.4 or more per 100,000 people. To adjust for variation in sample fecal content, four normalization biomarkers were evaluated: crAssphage, pepper mild mottle virus, Bacteroides ribosomal RNA (rRNA), and human 18S rRNA. Of these, crAssphage displayed the least spatial and temporal variability. Both unnormalized SARS-CoV-2 RNA signal and signal normalized to crAssphage had positive and significant correlation with clinical testing data (Kendall's Tau-b (τ)=0.43 and 0.38, respectively), but no normalization biomarker strengthened the correlation with clinical testing data. Locational dependencies and the date associated with testing data impacted the lead time of wastewater for clinical trends, and no lead time was observed when the sample collection date (versus the result date) was used for both wastewater and clinical testing data. This study supports that trends in wastewater surveillance data reflect trends in COVID-19 disease occurrence and presents tools that could be applied to make wastewater signal more interpretable and comparable across studies.


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