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An allele-specific primer extension assay to quantify the proportion of B.1.1.7-specific SARS-CoV-2 RNA in wastewater
Tyson E Graber; Kamya Bhatnagar; Elisabeth Mercier; Meghan Fuzzen; Patrick M D'Aoust; Huy-Dung Hoang; Xin Tian; Syeda Tasneem Towhid; Julio Plaza Diaz; Tommy Alain; Ainslie Butler; Lawrence Goodridge; Mark Servos; Robert Delatolla.
Afiliación
  • Tyson E Graber; Children's Hospital of Eastern Ontario Research Institute
  • Kamya Bhatnagar; University of Ottawa
  • Elisabeth Mercier; University of Ottawa
  • Meghan Fuzzen; University of Waterloo
  • Patrick M D'Aoust; University of Ottawa
  • Huy-Dung Hoang; Children's Hospital of Eastern Ontario Research Institute
  • Xin Tian; University of Ottawa
  • Syeda Tasneem Towhid; University of Ottawa
  • Julio Plaza Diaz; Children's Hospital of Eastern Ontario Research Institute
  • Tommy Alain; Children's Hospital of Eastern Ontario Research Institute
  • Ainslie Butler; Simcoe Muskoka District Health Unit
  • Lawrence Goodridge; University of Guelph
  • Mark Servos; University of Waterloo
  • Robert Delatolla; University of Ottawa
Preprint en En | PREPRINT-MEDRXIV | ID: ppmedrxiv-21252041
ABSTRACT
The coronavirus disease 2019 (COVID-19) pandemic caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has claimed millions of lives to date. Antigenic drift has resulted in viral variants with putatively greater transmissibility, virulence, or both. Early and near real-time detection of these variants of concern (VOC) and the ability to accurately follow their incidence and prevalence in communities is wanting. Wastewater-based epidemiology (WBE), which uses nucleic acid amplification tests to detect viral fragments, is a faithful proxy of COVID-19 incidence and prevalence, and thus offers the potential to monitor VOC viral load in a given population. Here, we describe and validate a primer extension PCR strategy targeting a signature mutation in the N gene of SARS-CoV-2. This allows quantification of the proportional expression of B.1.1.7 versus non-B.1.1.7 alleles in wastewater without the need to employ quantitative RT-PCR standard curves. We show that the wastewater B.1.1.7 profile correlates with its clinical counterpart and benefits from a near real-time and facile data collection and reporting pipeline. This assay can be quickly implemented within a current SARS-CoV-2 WBE framework with minimal cost; allowing early and contemporaneous estimates of B.1.1.7 community transmission prior to, or in lieu of, clinical screening and identification. Our study demonstrates that this strategy can provide public health units with an additional and much needed tool to rapidly triangulate VOC incidence/prevalence with high sensitivity and lineage specificity.
Licencia
cc_by_nc_nd
Texto completo: 1 Colección: 09-preprints Base de datos: PREPRINT-MEDRXIV Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies Idioma: En Año: 2021 Tipo del documento: Preprint
Texto completo: 1 Colección: 09-preprints Base de datos: PREPRINT-MEDRXIV Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies Idioma: En Año: 2021 Tipo del documento: Preprint