Table 1.
Testing approaches for SARS-CoV-2 and types of antibody assays
| Type of assay | Readout and limitations | Current scale | References |
|---|---|---|---|
| Digital surveys | subjective report on symptoms, can help to identify new infection hotspots on the population scale | millions | e.g., Menni et al.15 |
| qRT-PCR (quantitative reverse-transcriptase PCR) | detection of acute infections, cannot detect SARS-CoV-2 after the infection has been cleared (3–4 weeks after onset of symptoms in most individuals) | hundreds of thousands to millions | e.g., Johns Hopkins University16 |
| Sequencing of SARS-CoV-2 strains | allows tracking of the origin of strains and phylogenetic relationships and could be used to associate mutations with pathogenicity | thousands | e.g., Lu et al.17 |
| Antibody tests | enables detection after infection has been cleared; limited use for detecting acute infection because antibodies are only produced 1–2 weeks after onset of symptoms | thousands to tens of thousands (see Table 2) | e.g., Kobokovich et al.,4018 Gronvall et al.,4319 National COVID Testing Scientific Advisory Panel et al.4920 |
| LFA (lateral flow assay) | also called rapid diagnostic test (RDT), fast point of care (result within minutes) at cost of accuracy | ||
| ELISA (enzyme-linked immunosorbent assay) and CLIA (chemiluminescent immunoassay) | lab tests requiring dedicated equipment and personnel, taking hours and yielding higher accuracy than LFAs | ||
| neutralization assay | more complex biological lab test, the only method to functionally test antibodies for their ability to hinder infection of cells by SARS-CoV-2 |