Evidence map›Paper›PMID 38106082›Full record

ArticlebioRxiv : the preprint server for biology2023

Activation of Protein Kinase R (PKR) Plays a Pro-Viral Role in Mammarenavirus Infected Cells.

Haydar Witwit, Roaa Khafaji, Arul Salaniwal, Arthur S Kim, Beatrice Cubitt, Nathaniel Jackson, Chengjin Ye, Susan R Weiss, Luis Martinez-Sobrido, Juan Carlos de la Torre

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. 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, 0 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 1 country.

Haydar WitwitDepartment of Immunology and Microbiology, The Scripps Research Institute, La Jolla, CA 92037.ORCID 0000-0002-0174-8454
Roaa KhafajiDepartment of Immunology and Microbiology, The Scripps Research Institute, La Jolla, CA 92037.ORCID 0009-0006-9142-4483
Arul SalaniwalDepartment of Immunology and Microbiology, The Scripps Research Institute, La Jolla, CA 92037.
Arthur S KimDepartment of Immunology and Microbiology, The Scripps Research Institute, La Jolla, CA 92037.
Beatrice CubittDepartment of Immunology and Microbiology, The Scripps Research Institute, La Jolla, CA 92037.
Nathaniel JacksonTexas Biomedical Research Institute, San Antonio, TX, USA.
Chengjin YeTexas Biomedical Research Institute, San Antonio, TX, USA.ORCID 0000-0002-1934-9494
Susan R WeissDepartment of Microbiology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA 19104.ORCID 0000-0002-8155-4528
Luis Martinez-SobridoTexas Biomedical Research Institute, San Antonio, TX, USA.ORCID 0000-0001-7084-0804
Juan Carlos de la TorreDepartment of Immunology and Microbiology, The Scripps Research Institute, La Jolla, CA 92037.ORCID 0000-0002-8171-8115
Scripps Research Institute · USTexas Biomedical Research Institute · USUniversity of Pennsylvania · US

Funding

MOLECULAR BASIS OF VIRAL PATHOGENESIST32AI007354 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI DE LA TORRE, JUAN C. · 1989 to 2020
$5.2M
Roles of the Nucleoprotein 3'-5' Exonuclease Domain in Arenavirus BiologyR01AI142985 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI DE LA TORRE, JUAN C., MARTINEZ-SOBRIDO, LUIS · 2019 to 2022
$1.8M
NIAID NIH HHS R01 AI142985NIAID NIH HHS T32 AI007354
6 · The paper itself

Abstract

Many viruses, including mammarenaviruses, have evolved mechanisms to counteract different components of the host cell innate immunity, which is required to facilitate robust virus multiplication. The double strand (ds)RNA sensor protein kinase receptor (PKR) pathway plays a critical role in the cell antiviral response. Whether PKR can restrict the multiplication of the Old World mammarenavirus lymphocytic choriomeningitis virus (LCMV) and the mechanisms by which LCMV may counteract the antiviral functions of PKR have not yet been investigated. Here we present evidence that LCMV infection results in very limited levels of PKR activation, but LCMV multiplication is enhanced in the absence of PKR. In contrast, infection with a recombinant LCMV with a mutation affecting the 3'-5' exonuclease (ExoN) activity of the viral nucleoprotein (NP) resulted in robust PKR activation in the absence of detectable levels of dsRNA, which was associated with severely restricted virus multiplication that was alleviated in the absence of PKR. However, pharmacological inhibition of PKR activation resulted in reduced levels of LCMV multiplication. These findings uncovered a complex role of the PKR pathway in LCMV-infected cells involving both pro-and antiviral activities.

Identifiers

PMID38106082
PMCPMC10723269
OpenAlexW4389410762

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.