Journal
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES
Volume 40, Issue 5, Pages 1063-1071Publisher
SPRINGER
DOI: 10.1007/s10096-021-04169-7
Keywords
SARS-CoV-2; COVID-19; Serology; Neutralizing antibodies; Immunofluorescence test; Seroprevalence
Categories
Funding
- Projekt DEAL
- Jurgen Manchot Foundation
- Heinz-Ansmann Foundation for AIDS research
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Evaluation and power of seroprevalence studies depend on the performed serological assays. This study compared four commercial serological tests and an in-house test for identifying SARS-CoV-2 seropositive individuals in a high-prevalence setting. Results showed that commercial assays detected antibodies in a higher percentage of individuals, and spike-based assays were better at predicting neutralization titer than nucleoprotein-based assays.
Evaluation and power of seroprevalence studies depend on the performed serological assays. The aim of this study was to assess four commercial serological tests from EUROIMMUN, DiaSorin, Abbott, and Roche as well as an in-house immunofluorescence and neutralization test for their capability to identify SARS-CoV-2 seropositive individuals in a high-prevalence setting. Therefore, 42 social and working contacts of a German super-spreader were tested. Consistent with a high-prevalence setting, 26 of 42 were SARS-CoV-2 seropositive by neutralization test (NT), and immunofluorescence test (IFT) confirmed 23 of these 26 positive test results (NT 61.9% and IFT 54.8% seroprevalence). Four commercial assays detected anti-SARS-CoV-2 antibodies in 33.3-40.5% individuals. Besides an overall discrepancy between the NT and the commercial assays regarding their sensitivity, this study revealed that commercial SARS-CoV-2 spike-based assays are better to predict the neutralization titer than nucleoprotein-based assays are.
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