Evidence map›Paper›PMID 33257477›Full record

ArticleJournal of virology2021

A Versatile Reporter System To Monitor Virus-Infected Cells and Its Application to Dengue Virus and SARS-CoV-2.

Felix Pahmeier, Christopher J Neufeldt, Berati Cerikan, Vibhu Prasad, Costantin Pape, Vibor Laketa, Alessia Ruggieri, Ralf Bartenschlager, Mirko Cortese

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
0.6field-weighted citation impact, top 20% of its field
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

29 citing papers in PubMed, 36 citations in OpenAlex.

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  8. Reporter-expressing viruses for antiviral drug discovery research.Frontiers in cellular and infection microbiology · 2025
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  20. Imaging Techniques: Essential Tools for the Study of SARS-CoV-2 Infection.Frontiers in cellular and infection microbiology · 2022
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Felix PahmeierDepartment of Infectious Diseases, Molecular Virology, University of Heidelberg, Heidelberg, Germany.ORCID 0000-0002-7445-2259
Christopher J NeufeldtDepartment of Infectious Diseases, Molecular Virology, University of Heidelberg, Heidelberg, Germany.
Berati CerikanDepartment of Infectious Diseases, Molecular Virology, University of Heidelberg, Heidelberg, Germany.
Vibhu PrasadDepartment of Infectious Diseases, Molecular Virology, University of Heidelberg, Heidelberg, Germany.ORCID 0000-0001-7450-607X
Costantin PapeHCI/IWR, Heidelberg University, Heidelberg, Germany.
Vibor LaketaGerman Center for Infection Research, Heidelberg partner site, Heidelberg, Germany.
Alessia RuggieriDepartment of Infectious Diseases, Molecular Virology, University of Heidelberg, Heidelberg, Germany.
Ralf BartenschlagerDepartment of Infectious Diseases, Molecular Virology, University of Heidelberg, Heidelberg, Germany ralf.bartenschlager@med.uni-heidelberg.de mirko.cortese@med.uni-heidelberg.de.ORCID 0000-0001-5601-9307
Mirko CorteseDepartment of Infectious Diseases, Molecular Virology, University of Heidelberg, Heidelberg, Germany ralf.bartenschlager@med.uni-heidelberg.de mirko.cortese@med.uni-heidelberg.de.ORCID 0000-0003-1786-4211
Heidelberg University · DEGerman Cancer Research Center · DEGerman Center for Infection Research · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Positive-strand RNA viruses have been the etiological agents in several major disease outbreaks over the last few decades. Examples of this include flaviviruses, such as dengue virus and Zika virus, which cause millions of yearly infections around the globe, and coronaviruses, such as SARS-CoV-2, the source of the current pandemic. The severity of outbreaks caused by these viruses stresses the importance of research aimed at determining methods to limit virus spread and to curb disease severity. Such studies require molecular tools to decipher virus-host interactions and to develop effective treatments. Here, we describe the generation and characterization of a reporter system that can be used to visualize and identify cells infected with dengue virus or SARS-CoV-2. This system is based on viral protease activity that mediates cleavage and nuclear translocation of an engineered fluorescent protein stably expressed in cells. We show the suitability of this system for live cell imaging, for visualization of single infected cells, and for screening and testing of antiviral compounds. With the integrated modular building blocks, this system is easy to manipulate and can be adapted to any virus encoding a protease, thus offering a high degree of flexibility.

Indexed as

A549 CellsAnimalsCell LineChlorocebus aethiopsCOVID-19DengueDengue VirusGenes, ReporterGreen Fluorescent ProteinsHEK293 CellsHumansNuclear Localization SignalsSARS-CoV-2Vero CellsViral Nonstructural ProteinsVirus ReplicationGreen Fluorescent ProteinsNuclear Localization SignalsViral Nonstructural Proteinsdengue viruslive cell imagingreporter cell linesreporter systemSARS-CoV-2viral proteases

Identifiers

PMID33257477
PMCPMC7851548
OpenAlexW3110087867

What OpenQuestion holds

Textmetadata
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.