Evaluation of Severe Acute Respiratory Syndrome Coronavirus 2 Nucleocapsid Antigen in the Blood as a Diagnostic Test for Infection and Infectious Viral Shedding

Author:

Mathur Sujata123,Davidson Michelle C34,Anglin Khamal23,Lu Scott123,Goldberg Sarah A123,Garcia-Knight Miguel5,Tassetto Michel5,Zhang Amethyst5,Romero Mariela23,Pineda-Ramirez Jesus23,Diaz-Sanchez Ruth23,Rugart Paulina23,Chen Jessica Y23,Donohue Kevin4,Shak Joshua R6,Chenna Ahmed7,Winslow John W7,Petropoulos Christos J7,Yee Brandon C7,Lambert Jeremy8,Glidden David V1,Rutherford George W12,Deeks Steven G9,Peluso Michael J9,Andino Raul5,Martin Jeffrey N1,Kelly J Daniel1236

Affiliation:

1. Department of Epidemiology and Biostatistics, University of California , San Francisco, California , USA

2. Institute for Global Health Sciences, University of California , San Francisco, California , USA

3. Francis I. Proctor Foundation, University of California , San Francisco, California , USA

4. School of Medicine, University of California , San Francisco, California , USA

5. Department of Microbiology and Immunology, University of California , San Francisco, California , USA

6. San Francisco Veterans Affairs Medical Center , San Francisco, California , USA

7. Labcorp-Monogram Biosciences , South San Francisco, California , USA

8. Quanterix Laboratories , Billerica, Massachusetts , USA

9. Division of HIV, Infectious Disease, and Global Medicine, Department of Medicine, University of California , San Francisco, California , USA

Abstract

Abstract Background SARS-CoV-2 nucleocapsid antigen can be detected in plasma, but little is known about its performance as a diagnostic test for acute SARS-CoV-2 infection or infectious viral shedding among nonhospitalized individuals. Methods We used data generated from anterior nasal and blood samples collected in a longitudinal household cohort of SARS-CoV-2 cases and contacts. Participants were classified as true positives if polymerase chain reaction (PCR) positive for SARS-CoV-2 and as true negatives if PCR negative and seronegative. Infectious viral shedding was determined by the cytopathic effect from viral culture. Stratified by 7 days after symptom onset, we constructed receiver operating characteristic (ROC) curves to describe optimized accuracy (Youden index), optimized sensitivity, and specificity. Results Of 80 participants, 58 (73%) were true positives while 22 (27%) were true negatives. Using the manufacturer's cutoff of 1.25 pg/mL for evaluating infection, sensitivity was higher from 0 to 7 days (77.6% [95% confidence interval {CI}, 64%–88.2%]) than from 8 to 14 days (43.2% [95% CI, 31.1%–54.5%]) after symptom onset; specificity was unchanged at 100% (95% CI, 88.1%–100%). This test had higher sensitivity (100% [95% CI, 88.4%–100%]) and lower specificity (65% [95% CI, 40.8%–84.6%]) for infectious viral shedding as compared with infection, particularly within the first week of symptom onset. Although the presence of N-antigen correlated with infectious viral shedding (r = 0.63; P < .01), sensitivity still declined over time. Additional cutoffs from ROC curves were identified to optimize sensitivity and specificity. Conclusions We found that this SARS-CoV-2 N-antigen test was highly sensitive for detecting early but not late infectious viral shedding, making it a viable screening test for community-dwelling individuals to inform isolation practices.

Funder

Centers for Disease Control and Prevention Broad Agency Announcement

National Institute of Allergy and Infectious Diseases

NIH

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Oncology

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