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Comparison of SARS-CoV-2 serological assays for use in epidemiological surveillance in Scotland
Lindsay McDonald; Helen Wise; Frauke Muecksch; Daniel Poston; Sally Mavin; Kate Templeton; Elizabeth Furrie; Claire Richardson; Jacqueline McGuire; Lisa Jarvis; Kristen Malloy; Andrew McAuley; Norah Palmateer; Elizabeth Dickson; Theodora Hatziioannou; Paul Bieniasz; Sara Jenks.
Affiliation
  • Lindsay McDonald; Royal Infirmary of Edinburgh, NHS Lothian, Edinburgh, Scotland
  • Helen Wise; Royal Infirmary of Edinburgh, NHS Lothian, Edinburgh, Scotland
  • Frauke Muecksch; Laboratory of Retrovirology, The Rockefeller University, New York, New York, USA
  • Daniel Poston; Laboratory of Retrovirology, The Rockefeller University, New York, New York, USA
  • Sally Mavin; Scottish Microbiology Reference Laboratory, NHS Highland, Inverness, Scotland
  • Kate Templeton; Royal Infirmary of Edinburgh, NHS Lothian, Edinburgh, Scotland
  • Elizabeth Furrie; Ninewells Hospital and Medical School, NHS Tayside, Dundee, Scotland
  • Claire Richardson; University Hospital Monklands, NHS Lanarkshire, Airdrie, Scotland
  • Jacqueline McGuire; University Hospital Monklands, NHS Lanarkshire, Airdrie, Scotland
  • Lisa Jarvis; Scottish National Blood Transfusion Service, The Jack Copland Centre, Edinburgh, Scotland
  • Kristen Malloy; Scottish National Blood Transfusion Service, The Jack Copland Centre, Edinburgh, Scotland
  • Andrew McAuley; Public Health Scotland, Glasgow, Scotland; School of Health & Life Sciences, Glasgow Caledonian University, Glasgow, Scotland
  • Norah Palmateer; Public Health Scotland, Glasgow, Scotland; School of Health & Life Sciences, Glasgow Caledonian University, Glasgow, Scotland
  • Elizabeth Dickson; Public Health Scotland, Glasgow, Scotland
  • Theodora Hatziioannou; Laboratory of Retrovirology, The Rockefeller University, New York, New York, USA
  • Paul Bieniasz; The Rockefeller University, New York, New York, USA
  • Sara Jenks; Royal Infirmary of Edinburgh, NHS Lothian, Edinburgh, Scotland
Preprint in English | medRxiv | ID: ppmedrxiv-21255596
Journal article
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ABSTRACT
BackgroundSero-surveillance of SARS-CoV-2 is crucial to monitoring levels of population exposure and informing public health responses, but may be influenced by variability in performance between available assays. MethodsFive commercial immunoassays and a neutralising activity assay were used to detect antibodies to SARS-CoV-2 in routine primary care and paediatric samples collected during the first wave of the pandemic in NHS Lothian, Scotland as part of ongoing surveillance efforts. For each assay, sensitivity and specificity was calculated relative to consensus results and neutralising activity. Quantitative correlation was performed between serological and neutralising titres. ResultsSeroprevalence ranged from 3.4-7.3 % in primary care patients and 3-5.9 % in paediatric patients according to different immunoassays. Neutralising activity was detectable in 2.8 % and 1.3 % respectively. Relative assay performance changed depending on comparison to immunoassay consensus versus neutralising activity and qualititative versus quantitative agreement. Cross-reactivity with endemic seasonal coronaviruses was confirmed by neutralising assay in false positives for one immunoassay. Presence of false positives for another assay was found specifically in paediatric but not adult samples. ConclusionsFive serological assays show variable accuracy when applied to the general population, impacting seroprevalence estimates. Assay performance may also vary in detection of protective neutralising antibody levels. These aspects should be considered in assay selection and interpretation in epidemiological studies.
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Full text: Available Collection: Preprints Database: medRxiv Type of study: Diagnostic study / Observational study / Rct Language: English Year: 2021 Document type: Preprint
Full text: Available Collection: Preprints Database: medRxiv Type of study: Diagnostic study / Observational study / Rct Language: English Year: 2021 Document type: Preprint
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