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Integrated Antigenic and Nucleic Acid Detection in Single Virions and Extracellular Vesicles with Viral Content.

Authors :
Nguyen KT
Rima XY
Nguyen LTH
Wang X
Kwak KJ
Yoon MJ
Li H
Chiang CL
Doon-Ralls J
Scherler K
Fallen S
Godfrey SL
Wallick JA
Magaña SM
Palmer AF
Lee I
Nunn CC
Reeves KM
Kaplan HG
Goldman JD
Heath JR
Wang K
Pancholi P
Lee LJ
Reátegui E
Source :
Advanced healthcare materials [Adv Healthc Mater] 2024 May 31, pp. e2400622. Date of Electronic Publication: 2024 May 31.
Publication Year :
2024
Publisher :
Ahead of Print

Abstract

Virion-mediated outbreaks are imminent and despite rapid responses, continue to cause adverse symptoms and death. Therefore, tunable, sensitive, high-throughput assays are needed to help diagnose future virion-mediated outbreaks. Herein, it is developed a tunable in situ assay to selectively enrich virions and extracellular vesicles (EVs) and simultaneously detect antigens and nucleic acids at a single-particle resolution. The Biochip Antigen and RNA Assay (BARA) enhanced sensitivities compared to quantitative reverse-transcription polymerase chain reaction (qRT-PCR), enabling the detection of virions in asymptomatic patients, genetic mutations in single virions, and enabling the continued long-term expression of viral RNA in the EV-enriched subpopulation in the plasma of patients with post-acute sequelae of the coronavirus disease of 2019 (COVID-19). BARA revealed highly accurate diagnoses of COVID-19 by simultaneously detecting the spike glycoprotein and nucleocapsid-encoding RNA in saliva and nasopharyngeal swab samples. Altogether, the single-particle detection of antigens and viral RNA provides a tunable framework for the diagnosis, monitoring, and mutation screening of current and future outbreaks.<br /> (© 2024 The Author(s). Advanced Healthcare Materials published by Wiley‐VCH GmbH.)

Details

Language :
English
ISSN :
2192-2659
Database :
MEDLINE
Journal :
Advanced healthcare materials
Publication Type :
Academic Journal
Accession number :
38820600
Full Text :
https://doi.org/10.1002/adhm.202400622