Development and Implementation of Dried Blood Spot-based COVID-19 Serological Assays for Epidemiologic Studies

Author:

Wong Marcus P,Meas Michelle A,Adams Cameron,Hernandez Samantha,Green Valerie,Montoya Magelda,Hirsch Brett M,Horton Mary,Quach Hong L,Quach Diana L,Shao Xiaorong,Fedrigo Indro,Zermeno Alexandria,Huffaker Julia,Montes Raymond,Madden Alicia,Cyrus Sherri,McDowell David,Williamson Phillip,Contestable Paul,Stone Mars,Coloma Josefina,Busch Michael P,Barcellos Lisa F,Harris Eva

Abstract

AbstractSerological surveillance studies of infectious diseases provide population-level estimates of infection and antibody prevalence, generating crucial insight into population-level immunity, risk factors leading to infection, and effectiveness of public health measures. These studies traditionally rely on detection of pathogen-specific antibodies in samples derived from venipuncture, an expensive and logistically challenging aspect of serological surveillance. During the COVID-19 pandemic, guidelines implemented to prevent the spread of SARS-CoV-2 infection made collection of venous blood logistically difficult at a time when SARS-CoV-2 serosurveillance was urgently needed. Dried blood spots (DBS) have generated interest as an alternative to venous blood for SARS-CoV-2 serological applications due to their stability, low cost, and ease of collection; DBS samples can be self-generated via fingerprick by community members and mailed at ambient temperatures. Here, we detail the development of four DBS-based SARS-CoV-2 serological methods and demonstrate their implementation in a large serological survey of community members from 12 cities in the East Bay region of the San Francisco metropolitan area using at- home DBS collection. We find that DBS perform similarly to plasma/serum in enzyme-linked immunosorbent assays and commercial SARS-CoV-2 serological assays. In addition, we show that DBS samples can reliably detect antibody responses months post-infection and track antibody kinetics after vaccination. Implementation of DBS enabled collection of valuable serological data from our study population to investigate changes in seroprevalence over an eight-month period. Our work makes a strong argument for the implementation of DBS in serological studies, not just for SARS-CoV-2, but any situation where phlebotomy is inaccessible.

Publisher

Cold Spring Harbor Laboratory

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