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Simultaneous detection of SARS-CoV-2, influenza A, respiratory syncytial virus, and measles in wastewater by multiplex RT-qPCR.
Hayes, Emalie K; Gouthro, Madison T; LeBlanc, Jason J; Gagnon, Graham A.
  • Hayes EK; Centre for Water Resources Studies, Department of Civil & Resource Engineering, Dalhousie University, 1360 Barrington Street, Halifax, Nova Scotia B3H 4R2, Canada.
  • Gouthro MT; Centre for Water Resources Studies, Department of Civil & Resource Engineering, Dalhousie University, 1360 Barrington Street, Halifax, Nova Scotia B3H 4R2, Canada.
  • LeBlanc JJ; Department of Pathology, Dalhousie University, Canada; Department of Microbiology and Immunology, Dalhousie University, Canada; Department of Medicine (Infectious Diseases), Dalhousie University, Canada; Division of Microbiology, Department of Pathology and Laboratory Medicine, Nova Scotia Health, H
  • Gagnon GA; Centre for Water Resources Studies, Department of Civil & Resource Engineering, Dalhousie University, 1360 Barrington Street, Halifax, Nova Scotia B3H 4R2, Canada. Electronic address: Graham.gagnon@dal.ca.
Sci Total Environ ; 889: 164261, 2023 Sep 01.
Article in English | MEDLINE | ID: covidwho-2315264
ABSTRACT
A multiplex quantitative reverse transcription polymerase chain reaction (RT-qPCR)-based method was designed for the simultaneous detection of influenza A, SARS-CoV-2, respiratory syncytial virus, and measles virus. The performance of the multiplex assay was compared to four monoplex assays for relative quantification using standard quantification curves. Results showed that the multiplex assay had comparable linearity and analytical sensitivity to the monoplex assays, and the quantification parameters of both assays demonstrated minimal differences. Viral reporting recommendations for the multiplex method were estimated based on the corresponding limit of quantification (LOQ) and the limit of detection at 95 % confidence interval (LOD) values for each viral target. The LOQ was determined by the lowest nominal RNA concentrations where %CV values were ≤35 %. Corresponding LOD values for each viral target were between 15 and 25 gene copies per reaction (GC/rxn), and LOQ values were within 10 to 15 GC/rxn. The detection performance of a new multiplex assay was validated in the field by collecting composite wastewater samples from a local treatment facility and passive samples from three sewer shed locations. Results indicated that the assay could accurately estimate viral loads from various sample types, with samples collected from passive samplers showing a greater range of detectable viral concentrations than composite wastewater samples. This suggests that the sensitivity of the multiplex method may be improved when paired with more sensitive sampling methods. Laboratory and field results demonstrate the robustness and sensitivity of the multiplex assay and its applicability to detect the relative abundance of four viral targets among wastewater samples. Conventional monoplex RT-qPCR assays are suitable for diagnosing viral infections. However, multiplex analysis using wastewater provides a fast and cost-effective way to monitor viral diseases in a population or environment.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Virus Diseases / Influenza, Human / COVID-19 / Measles Type of study: Diagnostic study / Prognostic study Limits: Humans Language: English Journal: Sci Total Environ Year: 2023 Document Type: Article Affiliation country: J.scitotenv.2023.164261

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Virus Diseases / Influenza, Human / COVID-19 / Measles Type of study: Diagnostic study / Prognostic study Limits: Humans Language: English Journal: Sci Total Environ Year: 2023 Document Type: Article Affiliation country: J.scitotenv.2023.164261