Evidence map›Paper›PMID 37986994›Full record

ArticlebioRxiv : the preprint server for biology2024

Nanoscale cellular organization of viral RNA and proteins in SARS-CoV-2 replication organelles.

Leonid Andronov, Mengting Han, Yanyu Zhu, Ashwin Balaji, Anish R Roy, Andrew E S Barentine, Puja Patel, Jaishree Garhyan, Lei S Qi, W E Moerner

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 2 countries.

Leonid AndronovDepartment of Chemistry; Stanford University, Stanford, CA 94305 U.S.A.ORCID 0000-0002-4213-5363
Mengting HanDepartment of Bioengineering; Stanford University, Stanford, CA 94305 U.S.A.
Yanyu ZhuDepartment of Bioengineering; Stanford University, Stanford, CA 94305 U.S.A.
Ashwin BalajiDepartment of Chemistry; Stanford University, Stanford, CA 94305 U.S.A.
Anish R RoyDepartment of Chemistry; Stanford University, Stanford, CA 94305 U.S.A.
Andrew E S BarentineDepartment of Chemistry; Stanford University, Stanford, CA 94305 U.S.A.
Puja PatelIn Vitro Biosafety Level 3 (BSL-3) Service Center, School of Medicine; Stanford University, Stanford, CA 94305 U.S.A.
Jaishree GarhyanIn Vitro Biosafety Level 3 (BSL-3) Service Center, School of Medicine; Stanford University, Stanford, CA 94305 U.S.A.
Lei S QiDepartment of Bioengineering; Stanford University, Stanford, CA 94305 U.S.A.
W E MoernerDepartment of Chemistry; Stanford University, Stanford, CA 94305 U.S.A.
Stanford University · USBioengineering Center · RUChan Zuckerberg Initiative (United States) · US

Funding

Single-Molecule Imaging for Cell Biology and Super-Resolution MicroscopyR35GM118067 · NIGMS · STANFORD UNIVERSITY · PI MOERNER, WILLIAM E · 2016 to 2025
$6.2M
Engineering and Imaging 3D genome structure-function dynamics across time scalesU01DK127405 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI BLOBEL, GERD A, PHILLIPS-CREMINS, JENNIFER ELIZABETH · 2020 to 2024
$5.7M
NIDDK NIH HHS U01 DK127405NIGMS NIH HHS R35 GM118067
6 · The paper itself

Abstract

The SARS-CoV-2 viral infection transforms host cells and produces special organelles in many ways, and we focus on the replication organelle where the replication of viral genomic RNA (vgRNA) occurs. To date, the precise cellular localization of key RNA molecules and replication intermediates has been elusive in electron microscopy studies. We use super-resolution fluorescence microscopy and specific labeling to reveal the nanoscopic organization of replication organelles that contain vgRNA clusters along with viral double-stranded RNA (dsRNA) clusters and the replication enzyme, encapsulated by membranes derived from the host endoplasmic reticulum (ER). We show that the replication organelles are organized differently at early and late stages of infection. Surprisingly, vgRNA accumulates into distinct globular clusters in the cytoplasmic perinuclear region, which grow and accommodate more vgRNA molecules as infection time increases. The localization of ER labels and nsp3 (a component of the double-membrane vesicle, DMV) at the periphery of the vgRNA clusters suggests that replication organelles are enclosed by DMVs at early infection stages which then merge into vesicle packets as infection progresses. Precise co-imaging of the nanoscale cellular organization of vgRNA, dsRNA, and viral proteins in replication organelles of SARS-CoV-2 may inform therapeutic approaches that target viral replication and associated processes.

Indexed as

cell infectionCOVID-19fluorescence imagingSARS-CoV-2 coronavirussuper-resolution fluorescence microscopyviral proteinsviral replicationviral RNA localization

Identifiers

PMID37986994
PMCPMC10659379
OpenAlexW4388511458

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.