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

Kim Truc Nguyen
Xilal Y Rima
Luong T H Nguyen
Xinyu Wang
Kwang Joo Kwak
Min Jin Yoon
Hong Li
Chi-Ling Chiang
Jacob Doon-Ralls
Kelsey Scherler, Institute for Systems Biology, Seattle, WA, 98109, USA.
Shannon Fallen, Institute for Systems Biology, Seattle, WA, 98109, USA.
Stephanie L Godfrey, Providence Swedish Medical Center, Seattle, WA, 98104, USA.
Julie A Wallick, Providence Swedish Medical Center, Seattle, WA, 98104, USA.
Setty M Magaña
Andre F Palmer
Inyoul Lee, Institute for Systems Biology, Seattle, WA, 98109, USA.
Christopher C. Nunn, Providence Swedish Medical Center, Seattle, WA, 98104, USA.
Kimberly M Reeves, Providence Swedish Cancer Institute, Seattle, WA, 98104, USA.
Henry G Kaplan, Providence Swedish Cancer Institute, Seattle, WA, 98104, USA.
Jason D Goldman, Providence Swedish Medical Center, Seattle, WA, 98104, USA.
James R Heath, Institute for Systems Biology, Seattle, WA, 98109, USA.
Kai Wang, Institute for Systems Biology, Seattle, WA, 98109, USA.
Preeti Pancholi
L James Lee
Eduardo Reátegui

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.