Severe Acute Respiratory Syndrome Coronavirus 2--Reactive Salivary Antibody Detection in South Carolina Emergency Healthcare Workers: September 2019 -- March 2020

Abstract

Background: On 19 January 2020, the first case of severe acute respiratory syndrome coronavirus 2 (SARS–CoV–2) infection was identified in the US, with the first cases in South Carolina (SC) confirmed on 06 March 2020. Due to initial limited testing capabilities and potential for asymptomatic transmission, it is possible that the virus was present earlier than previously thought while preexisting immunity in at–risk populations was unknown. Methods: Salivary samples from 55 SC emergency department physicians, Emergency Medical Services (EMS) providers, and medical students working as EMTs were collected from September 2019 to March 2020 as part of a separate study and stored frozen. To determine if antibody-based immunity to SARS–CoV–2 was present prior to the first recorded cases, saliva acquired post–shift was analyzed by Enzyme–Linked Immunosorbent Assay with repeat of positive or inconclusive results and follow–up testing of pre–shift samples. Results: Two participants were positive for SARS–CoV–2–reactive salivary IgG, confirmed by repeat and follow–up testing. Positive samples were from medical students working in EMS and were collected in October or November 2019. Conclusions: The presence of detectable antibodies against SARS–CoV–2 in 2019 suggests that immunity existed in SC, and the US as a whole, prior to the earliest documented cases of COVID–19. Additionally, successful analysis of banked salivary samples demonstrates the feasibility of saliva as a noninvasive tool for surveillance of emerging outbreaks. These findings suggest that emergency healthcare providers represent a high–risk population that should be the focus of infectious disease surveillance.

Competing Interest Statement

The authors have declared no competing interest.

Funding Statement

This study was funded by a Transformative Seed Grant from the Health Sciences Center at Prisma Health.

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

Yes

The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

The Institutional Review Board of Prisma Health gave ethical approval for this work

I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.

Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

Yes

I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.

Yes

Data Availability

All data produced in the present study are available upon reasonable request to the authors.

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