Salivary testing of COVID-19: evaluation of serological testing following positive salivary results

BMC Infect Dis. 2021 May 4;21(1):410. doi: 10.1186/s12879-021-06108-5.

Abstract

Background: Salivary detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has been proposed as an alternative to nasopharyngeal or oropharyngeal swab testing. Our group previously published a study demonstrating that both testing methods identified SARS-CoV-2 using polymerase chain reaction (PCR)-based detection methodology. We therefore conducted a follow-up study using antibody testing to evaluate the accuracy of saliva versus swabs for COVID-19 detection and the durability of antibody response.

Methods: Venous blood samples were collected from consenting participants and the presence of serum antibodies for SARS-CoV-2 was evaluated on a large, automated immunoassay platform by the Roche anti-SARS-CoV-2 qualitative assay (Roche Diagnostics, Laval Quebec). Individuals with a serum antibody cut-off index (COI) ≥ 1.0 were considered positive.

Results: In asymptomatic and mildly symptomatic patients with a previously positive standard swab and/or saliva SARS-CoV-2 PCR-test, 42 demonstrated antibodies with 13 patients positive by swab alone, and 8 patients positive by saliva alone.

Conclusions: Despite their status as 'current standard' for COVID-19 testing, these findings highlight limitations of PCR-based tests.

Keywords: Antibodies; COVID-19; Coronavirus; SARS-CoV-2; Saliva.

Publication types

  • Evaluation Study

MeSH terms

  • Adult
  • Aged
  • Antibodies, Viral / analysis
  • Antibodies, Viral / blood
  • COVID-19 / immunology*
  • COVID-19 Nucleic Acid Testing / methods
  • COVID-19 Serological Testing / methods*
  • Female
  • Follow-Up Studies
  • Humans
  • Immunity, Humoral
  • Male
  • Middle Aged
  • Nasopharynx / virology
  • Polymerase Chain Reaction
  • SARS-CoV-2 / genetics
  • SARS-CoV-2 / immunology
  • Saliva / virology*
  • Time Factors

Substances

  • Antibodies, Viral