Developing and validating SARS‐CoV‐2 assays for nonhuman primate surveillance

Introduction In early 2020, the California National Primate Research Center implemented surveillance to address the threat of SARS‐CoV‐2 infection in its nonhuman primate colony. Materials/Methods To detect antiviral antibodies, multi‐antigen assays were developed and validated on enzyme immunoassay...

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Published in:Journal of medical primatology Vol. 51; no. 5; pp. 264 - 269
Main Authors: Yee, JoAnn, Carpenter, Amanda, Nham, Peter, Halley, Bryson, Van Rompay, Koen K. A., Roberts, Jeffrey
Format: Journal Article
Language:English
Published: Denmark Wiley Subscription Services, Inc 01.10.2022
John Wiley and Sons Inc
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ISSN:0047-2565, 1600-0684, 1600-0684
Online Access:Get full text
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Summary:Introduction In early 2020, the California National Primate Research Center implemented surveillance to address the threat of SARS‐CoV‐2 infection in its nonhuman primate colony. Materials/Methods To detect antiviral antibodies, multi‐antigen assays were developed and validated on enzyme immunoassay and multiplex microbead immunofluorescent assay (MMIA) platforms. To detect viral RNA, RT‐PCR was also performed. Results/Conclusion Using a 4plex, antibody was identified in 16/16 experimentally infected animals; and specificity for spike, nucleocapsid, receptor binding domain, and whole virus antigens was 95.2%, 93.8%, 94.3%, and 97.1%, respectively on surveillance samples. Six laboratories compared this MMIA favorably with nine additional laboratory‐developed or commercially available assays. Using a screen and confirm algorithm, 141 of the last 2441 surveillance samples were screen‐reactive requiring confirmatory testing. Although 35 samples were reactive to either nucleocapsid or spike; none were reactive to both. Over 20 000 animals have been tested and no spontaneous infections have so far been confirmed across the NIH sponsored National Primate Research Centers.
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ISSN:0047-2565
1600-0684
1600-0684
DOI:10.1111/jmp.12604