Evidence map›Paper›PMID 36851515›Full record

ArticleViruses2023

Differential Cellular Sensing of Fusion from within and Fusion from without during Virus Infection.

David N Hare, Tetyana Murdza, Susan Collins, Katharina Schulz, Subhendu Mukherjee, Roberto de Antueno, Luke Janssen, Roy Duncan, Karen L Mossman

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 36% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Expulsion of nuclear DNA to the cytoplasm after viral entry: A mechanism for activation of the cGAS pathway.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Article
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.

David N HareDepartment of Biochemistry and Biomedical Sciences, Institute for Infectious Disease Research, McMaster University, Hamilton, ON L8S 4K1, Canada.
Tetyana MurdzaDepartment of Biochemistry and Biomedical Sciences, Institute for Infectious Disease Research, McMaster University, Hamilton, ON L8S 4K1, Canada.
Susan CollinsDepartment of Biochemistry and Biomedical Sciences, Institute for Infectious Disease Research, McMaster University, Hamilton, ON L8S 4K1, Canada.
Katharina SchulzDepartment of Biochemistry and Biomedical Sciences, Institute for Infectious Disease Research, McMaster University, Hamilton, ON L8S 4K1, Canada.
Subhendu MukherjeeDepartment of Medicine, McMaster University, Hamilton, ON L8S 4K1, Canada.
Roberto de AntuenoDepartment of Microbiology and Immunology, Dalhousie University, Halifax, NS B3H 4R2, Canada.
Luke JanssenDepartment of Medicine, McMaster University, Hamilton, ON L8S 4K1, Canada.
Roy DuncanDepartment of Microbiology and Immunology, Dalhousie University, Halifax, NS B3H 4R2, Canada.ORCID 0000-0002-5162-5081
Karen L MossmanDepartment of Biochemistry and Biomedical Sciences, Institute for Infectious Disease Research, McMaster University, Hamilton, ON L8S 4K1, Canada.ORCID 0000-0002-1725-5873
McMaster University · CADalhousie University · CASt. Joseph’s Healthcare Hamilton · CA

Funding

CIHR FDN-143305CIHR PJT-148578
6 · The paper itself

Abstract

The physical entry of virus particles into cells triggers an innate immune response that is dependent on both calcium and nucleic acid sensors, with particles containing RNA or DNA genomes detected by RNA or DNA sensors, respectively. While membrane fusion in the absence of viral nucleic acid causes an innate immune response that is dependent on calcium, the involvement of nucleic acid sensors is poorly understood. Here, we used lipoplexes containing purified reovirus p14 fusion protein as a model of exogenous or fusion from without and a cell line expressing inducible p14 protein as a model of endogenous or fusion from within to examine cellular membrane fusion sensing events. We show that the cellular response to membrane fusion in both models is dependent on calcium, IRF3 and IFN. The method of sensing fusion, however, differs between fusion from without and fusion from within. Exogenous p14 lipoplexes are detected by RIG-I-like RNA sensors, whereas fusion by endogenous p14 requires both RIG-I and STING to trigger an IFN response. The source of nucleic acid that is sensed appears to be cellular in origin. Future studies will investigate the source of endogenous nucleic acids recognized following membrane fusion events.

Indexed as

Nucleic AcidsVirus DiseasesAntibodies, ViralCalciumHumansRNAAntibodies, ViralCalciumNucleic AcidsRNAinnate signalinginterferoninterferon regulatory factor 3membrane fusionvirus entryvirus–host interactions

Identifiers

PMID36851515
PMCPMC9962872
OpenAlexW4317735710

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.