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Updated: Nov 2, 2025

Visualization of SARS-CoV-2 using Immuno RNA-Fluorescence In Situ Hybridization
Published on: December 23, 2020
Multi-color super-resolution imaging to study human coronavirus RNA during cellular infection
Jiarui Wang1,2, Mengting Han3, Anish R Roy1
1Department of Chemistry, Chemical and Systems Biology, and ChEM-H Stanford University, Stanford, California, 94305 U.S.A.
Abstract:
The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the third human coronavirus within 20 years that gave rise to a life-threatening disease and the first to reach pandemic spread. To make therapeutic headway against current and future coronaviruses, the biology of coronavirus RNA during infection must be precisely understood. Here, we present a robust and generalizable framework combining high-throughput confocal and super-resolution microscopy imaging to study coronavirus infection at the nanoscale. Employing the model human coronavirus HCoV-229E, we specifically labeled coronavirus genomic RNA (gRNA) and double-stranded RNA (dsRNA) via multicolor RNA-immunoFISH and visualized their localization patterns within the cell. The exquisite resolution of our approach uncovers a striking spatial organization of gRNA and dsRNA into three distinct structures and enables quantitative characterization of the status of the infection after antiviral drug treatment. Our approach provides a comprehensive framework that supports investigations of coronavirus fundamental biology and therapeutic effects.
Insights
Understanding coronavirus RNA biology is key to developing new therapies. This study uses advanced microscopy to reveal distinct RNA structures during infection, aiding drug development for SARS-CoV-2 and future viruses.
Area of Science:
- Virology
- Molecular Biology
- Microscopy
Background:
- Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a pandemic-spreading virus, necessitating better therapeutic strategies.
- Understanding coronavirus RNA biology during infection is crucial for developing effective treatments against current and future threats.
Approach:
- Developed a robust framework combining high-throughput confocal and super-resolution microscopy for nanoscale study of coronavirus infection.
- Utilized multicolor RNA-immunoFISH to specifically label and visualize genomic RNA (gRNA) and double-stranded RNA (dsRNA) of human coronavirus HCoV-229E.
Key Points:
- The approach revealed a striking spatial organization of gRNA and dsRNA into three distinct structures within infected cells.
- Enabled quantitative characterization of infection status following antiviral drug treatment.
Conclusions:
- The presented framework supports fundamental research into coronavirus biology.
- Facilitates the investigation of therapeutic effects on coronavirus infection at the nanoscale.
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