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SARS-CoV-2 Protein in Wastewater Mirrors COVID-19 Prevalence.
Nafisa Neault; Aiman T. Baig; Tyson E. Graber; Patrick M. D'Aoust; Elisabeth Mercier; Ilya Alexandrov; Daniel Crosby; Janice Mayne; Thomas Pounds; Malcolm MacKenzie; Daniel Figeys; Alex E. MacKenzie; Robert Delatolla.
Affiliation
  • Nafisa Neault; Children's Hospital of Eastern Ontario Research Institute, Ottawa, Canada, K1H 8L1
  • Aiman T. Baig; Children's Hospital of Eastern Ontario Research Institute, Ottawa, Canada, K1H 8L1
  • Tyson E. Graber; Children's Hospital of Eastern Ontario Research Institute, Ottawa, Canada, K1H 8L1
  • Patrick M. D'Aoust; Department of Civil Engineering, University of Ottawa, Ottawa, Canada, K1N 6N5
  • Elisabeth Mercier; Department of Civil Engineering, University of Ottawa, Ottawa, Canada, K1N 6N5
  • Ilya Alexandrov; ActivSignal LLC., Natick, MA, United States, 01760
  • Daniel Crosby; ActivSignal LLC., Natick, MA, United States, 01760
  • Janice Mayne; Department of Biochemistry, Microbiology and Immunology, University of Ottawa, Ottawa, Canada, K1H 8M5
  • Thomas Pounds; ActivSignal LLC., Natick, MA, United States, 01760
  • Malcolm MacKenzie; ActivSignal LLC., Natick, MA, United States, 01760
  • Daniel Figeys; Department of Biochemistry, Microbiology and Immunology, University of Ottawa, Ottawa, Canada, K1H 8M5; Department of Chemistry and Biomolecular Sciences, Unive
  • Alex E. MacKenzie; Children's Hospital of Eastern Ontario Research Institute, Ottawa, Canada, K1H 8L1
  • Robert Delatolla; Department of Civil Engineering, University of Ottawa, Ottawa, Canada, K1N 6N5
Preprint in English | medRxiv | ID: ppmedrxiv-20185280
ABSTRACT
The COVID-19 pandemic has given rise to diverse approaches to track infections. The causative agent, SARS-CoV-2, is a fecally-shed RNA virus, and many groups have assayed wastewater for viral RNA fragments by quantitative reverse transcription polymerase chain reaction (qRT-PCR) as a proxy for COVID-19 prevalence in the community. Most groups report low levels of viral RNA that often skirt the methods theoretical limits of detection and quantitation. Here, we demonstrate the presence of SARS-CoV-2 structural proteins in wastewater using traditional immunoblotting and quantitate them from wastewater solids using an immuno-linked PCR method called Multiplex Paired-antibody Amplified Detection (MPAD). MPAD demonstrated facile detection of SARS-CoV-2 proteins compared with SARS-CoV-2 RNA via qRT-PCR in wastewater. In this longitudinal study, we corrected for stochastic variability inherent to wastewater-based epidemiology using multiple fecal content protein biomarkers. These normalized SARS-CoV-2 protein data correlated well with public health metrics. Our method of assaying SARS-CoV-2 protein from wastewater represents a promising and sensitive epidemiological tool to assess prevalence of fecally-shed pathogens in the community.
License
cc_by_nc
Full text: Available Collection: Preprints Database: medRxiv Type of study: Cohort_studies / Diagnostic study / Experimental_studies / Observational study / Prognostic study / Rct Language: English Year: 2020 Document type: Preprint
Full text: Available Collection: Preprints Database: medRxiv Type of study: Cohort_studies / Diagnostic study / Experimental_studies / Observational study / Prognostic study / Rct Language: English Year: 2020 Document type: Preprint
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