| Literature DB >> 33795412 |
Thomas E Morrison1, Rosemary Rochford2,3, Ross M Kedl1, Jonathan S Schultz4, Mary K McCarthy1, Cody Rester1, Katherine R Sabourin1, Kyle Annen5, Melkon DomBourian5, Elan Eisenmesser6, Ashley Frazer-Abel7, Vijaya Knight5, Thomas Jaenisch3.
Abstract
Serological testing of large representative populations for antibodies to SARS-CoV-2 is needed to estimate seroprevalence, transmission dynamics, and the duration of antibody responses from natural infection and vaccination. In this study, a high-throughput SARS-CoV-2 multiplex microsphere immunoassay (MMIA) was developed for the receptor binding domain (RBD) and nucleocapsid (N) that was more sensitive than enzyme-linked immunosorbent assay (ELISA) (98% versus 87%). The MMIA was then applied and validated in 264 first responders in Colorado using serum and dried blood spot (DBS) eluates, compared to ELISA, and evaluated for neutralizing antibodies. Four percent (11/264) of first responders were seropositive in July to August 2020. Serum and DBS were highly correlated for anti-RBD and anti-N antibodies (R = 0.83, P < 0.0001 and R = 0.87, P < 0.0001, respectively) by MMIA. The MMIA accurately predicted SARS-CoV-2 neutralizing antibodies using DBS (R = 0.76, P = 0.037). On repeat antibody testing 3 months later, anti-RBD IgG decreased less rapidly than anti-N IgG measured by MMIA, with a median change in geometric median fluorescence intensity of 62% versus 79% (P < 0.01) for anti-RBD and anti-N IgG, respectively. This novel MMIA using DBS could be scalable for rapid and affordable SARS-CoV-2 serosurveillance in the United States and globally.Entities:
Keywords: COVID-19 antibody testing; SARS-CoV-2 infection serological testing; dried blood spot testing; enzyme immunoassay; immunological surveillance
Year: 2021 PMID: 33795412 DOI: 10.1128/JCM.00290-21
Source DB: PubMed Journal: J Clin Microbiol ISSN: 0095-1137 Impact factor: 5.948