A Single-Round Infection Fluorescent SARS-CoV-2 Neutralization Test for COVID-19 Serological Testing at a Biosafety Level-2 Laboratory.


Journal

Viruses
ISSN: 1999-4915
Titre abrégé: Viruses
Pays: Switzerland
ID NLM: 101509722

Informations de publication

Date de publication:
02 06 2022
Historique:
received: 17 04 2022
revised: 28 05 2022
accepted: 29 05 2022
entrez: 24 6 2022
pubmed: 25 6 2022
medline: 28 6 2022
Statut: epublish

Résumé

A robust serological test to measure neutralizing antibodies against SARS-CoV-2 in biosafety level-2 (BSL-2) laboratories is useful for monitoring antibody response after vaccination or natural infection. The gold standard assay is the conventional plaque reduction neutralization test (PRNT) which requires extensive labor, live viruses, and BSL-3 facilities. Recently, we developed a novel single-round infection fluorescent SARS-CoV-2 virus (SFV) that can be safely used at BSL-2 laboratories for high-throughput neutralization and antiviral testing. In this study, we evaluated the performance of the neutralization test using this SFV with 80 PRNT-positive and 92 PRNT-negative clinical serum or plasma specimens. The SFV neutralization test (SFVNT) has 100% sensitivity and specificity compared to the PRNT. Furthermore, the neutralizing titers generated by the SFVNT and PRNT are highly correlated, with R2 = 0.903 (p < 0.0001). Due to high sensitivity, specificity, accuracy, and reproducibility, the SFVNT can be deployed for the large-scale testing of COVID-19 patients or vaccinated people in general lab settings.

Identifiants

pubmed: 35746682
pii: v14061211
doi: 10.3390/v14061211
pmc: PMC9230609
pii:
doi:

Substances chimiques

Antibodies, Neutralizing 0
Antibodies, Viral 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIH HHS
ID : HHSN272201600013C, AI134907, AI145617, and UL1TR001439
Pays : United States

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Auteurs

Jing Zou (J)

Department of Biochemistry & Molecular Biology, University of Texas Medical Branch, Galveston, TX 77555, USA.

Hongjie Xia (H)

Department of Biochemistry & Molecular Biology, University of Texas Medical Branch, Galveston, TX 77555, USA.

Pei-Yong Shi (PY)

Department of Biochemistry & Molecular Biology, University of Texas Medical Branch, Galveston, TX 77555, USA.
Institute for Human Infection and Immunity, University of Texas Medical Branch, Galveston, TX 77555, USA.
Sealy Institute for Drug Discovery, University of Texas Medical Branch, Galveston, TX 77555, USA.
Institute for Translational Sciences, University of Texas Medical Branch, Galveston, TX 77555, USA.
Sealy Institute for Vaccine Sciences, University of Texas Medical Branch, Galveston, TX 77555, USA.
Sealy Center for Structural Biology & Molecular Biophysics, University of Texas Medical Branch, Galveston, TX 77555, USA.

Xuping Xie (X)

Department of Biochemistry & Molecular Biology, University of Texas Medical Branch, Galveston, TX 77555, USA.
Institute for Human Infection and Immunity, University of Texas Medical Branch, Galveston, TX 77555, USA.

Ping Ren (P)

Institute for Human Infection and Immunity, University of Texas Medical Branch, Galveston, TX 77555, USA.
Department of Pathology, University of Texas Medical Branch, Galveston, TX 77555, USA.

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