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Comparative performance data for multiplex SARS-CoV-2 serological assays from a large panel of dried blood spot specimens.
Cholette, François; Fabia, Rissa; Harris, Angela; Ellis, Hannah; Cachero, Karla; Schroeder, Lukas; Mesa, Christine; Lacap, Philip; Arnold, Corey; Galipeau, Yannick; Langlois, Marc-André; Colwill, Karen; Gingras, Anne-Claude; McGeer, Allison; Giles, Elizabeth; Day, Jacqueline; Osiowy, Carla; Durocher, Yves; Hankins, Catherine; Mazer, Bruce; Drebot, Michael; Kim, John.
  • Cholette F; National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Canada.
  • Fabia R; Department of Medical Microbiology and Infectious Diseases, University of Manitoba, Winnipeg, Canada.
  • Harris A; National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Canada.
  • Ellis H; National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Canada.
  • Cachero K; National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Canada.
  • Schroeder L; National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Canada.
  • Mesa C; National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Canada.
  • Lacap P; National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Canada.
  • Arnold C; National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Canada.
  • Galipeau Y; Department of Biochemistry, Microbiology & Immunology, Faculty of Medicine, University of Ottawa, Canada.
  • Langlois MA; Department of Biochemistry, Microbiology & Immunology, Faculty of Medicine, University of Ottawa, Canada.
  • Colwill K; Department of Biochemistry, Microbiology & Immunology, Faculty of Medicine, University of Ottawa, Canada.
  • Gingras AC; The Centre for Infection, Immunity, and Inflammation (CI3), University of Ottawa, Ottawa, Canada.
  • McGeer A; Lunenfeld-Tanenbaum Research Institute at Mount Sinai Hospital, Sinai Health, Toronto, Canada.
  • Giles E; Lunenfeld-Tanenbaum Research Institute at Mount Sinai Hospital, Sinai Health, Toronto, Canada.
  • Day J; Department of Molecular Genetics, University of Toronto, Toronto, Canada.
  • Osiowy C; Lunenfeld-Tanenbaum Research Institute at Mount Sinai Hospital, Sinai Health, Toronto, Canada.
  • Durocher Y; Department of Microbiology at Mount Sinai Hospital, Sinai Health, Toronto, Canada.
  • Hankins C; Institute of Health Policy, Management and Evaluation, University of Toronto, Canada.
  • Mazer B; National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Canada.
  • Drebot M; National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Canada.
  • Kim J; National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Canada.
Heliyon ; 8(9): e10270, 2022 Sep.
Article in English | MEDLINE | ID: covidwho-2004106
ABSTRACT
The extent of the COVID-19 pandemic will be better understood through serosurveys and SARS-CoV-2 antibody testing. Dried blood spot (DBS) samples will play a central role in large scale serosurveillance by simplifying biological specimen collection and transportation, especially in Canada. Direct comparative performance data on multiplex SARS-CoV-2 assays resulting from identical DBS samples are currently lacking. In our study, we aimed to provide performance data for the BioPlex 2200 SARS-CoV-2 IgG (Bio-Rad), V-PLEX SARS-CoV-2 Panel 2 IgG (MSD), and Elecsys Anti-SARS-CoV-2 (Roche) commercial assays, as well as for two highly scalable in-house assays (University of Ottawa and Mount Sinai Hospital protocols) to assess their suitability for DBS-based SARS-CoV-2 DBS serosurveillance. These assays were evaluated against identical panels of DBS samples collected from convalescent COVID-19 patients (n = 97) and individuals undergoing routine sexually transmitted and bloodborne infection (STBBI) testing prior to the COVID-19 pandemic (n = 90). Our findings suggest that several assays are suitable for serosurveillance (sensitivity >97% and specificity >98%). In contrast to other reports, we did not observe an improvement in performance using multiple antigen consensus-based rules to establish overall seropositivity. This may be due to our DBS panel which consisted of samples collected from convalescent COVID-19 patients with significant anti-spike, -receptor binding domain (RBD), and -nucleocapsid antibody titers. This study demonstrates that biological specimens collected as DBS coupled with one of several readily available assays are useful for large-scale COVID-19 serosurveillance.
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Full text: Available Collection: International databases Database: MEDLINE Type of study: Experimental Studies Language: English Journal: Heliyon Year: 2022 Document Type: Article Affiliation country: J.heliyon.2022.e10270

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Experimental Studies Language: English Journal: Heliyon Year: 2022 Document Type: Article Affiliation country: J.heliyon.2022.e10270