Evidence map›Paper›PMID 35730940›Full record

ArticleMicrobiology spectrum2022

A 77 Amino Acid Region in the N-Terminal Half of the HSV-1 E3 Ubiquitin Ligase ICP0 Contributes to Counteracting an Established Type 1 Interferon Response.

Mirna Perusina Lanfranca, Jessica M van Loben Sels, Cindy Y Ly, Tristan R Grams, Adit Dhummakupt, David C Bloom, David J Davido

Open access · goldAbstract read
In one paragraph

Article in Microbiology spectrum, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 46% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. 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

7 authors at 2 institutions in 1 country.

Mirna Perusina LanfrancaDepartment of Molecular Biosciences, University of Kansasgrid.266515.3, Lawrence, Kansas, USA.
Jessica M van Loben SelsDepartment of Molecular Biosciences, University of Kansasgrid.266515.3, Lawrence, Kansas, USA.
Cindy Y LyDepartment of Molecular Biosciences, University of Kansasgrid.266515.3, Lawrence, Kansas, USA.
Tristan R GramsDepartment of Molecular Genetics and Microbiology, University of Floridagrid.15276.37 College of Medicine, Gainesville, Florida, USA.ORCID 0000-0002-2230-3745
Adit DhummakuptDepartment of Molecular Genetics and Microbiology, University of Floridagrid.15276.37 College of Medicine, Gainesville, Florida, USA.
David C BloomDepartment of Molecular Genetics and Microbiology, University of Floridagrid.15276.37 College of Medicine, Gainesville, Florida, USA.
David J DavidoDepartment of Molecular Biosciences, University of Kansasgrid.266515.3, Lawrence, Kansas, USA.
University of Kansas · USUniversity of Florida · US

Funding

Mentoring CoreP20GM103418 · NIGMS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI Douglas E Wright · 2012 to 2026
$63.0M
Molecular Genetics of HSV ReactivationR01AI048633 · NIAID · UNIVERSITY OF FLORIDA · PI BLOOM, DAVID C. · 2001 to 2023
$7.2M
BASIC MICROBIOLOGY &INFECTIOUS DISEASEST32AI007110 · NIAID · UNIVERSITY OF FLORIDA · PI Stephanie M Karst · 1985 to 2026
$4.3M
Viral and host responses to HSV infectionR01AI072357 · NIAID · UNIVERSITY OF KANSAS LAWRENCE · PI DAVIDO, DAVID J · 2007 to 2010
$1.3M
NIAID NIH HHS R01 AI048633NIAID NIH HHS R01 AI072357NIAID NIH HHS T32 AI007110NIGMS NIH HHS P20 GM103418
6 · The paper itself

Abstract

Herpes simplex virus 1 (HSV-1) is a human pathogen capable of establishing lifelong latent infections that can reactivate under stress conditions. A viral immediate early protein that plays important roles in the HSV-1 lytic and latent infections is the viral E3 ubiquitin ligase, ICP0. ICP0 transactivates all temporal classes of HSV-1 genes and facilitates viral gene expression. ICP0 also impairs the antiviral effects of interferon (IFN)-β, a component of host innate defenses known to limit viral replication. To begin to understand how ICP0 allows HSV-1 to disarm the IFN-β response, we performed genetic analyses using a series of ICP0 truncation mutants in the absence and presence of IFN-β in cell culture. We observed that IFN-β pretreatment of cells significantly impaired the replication of the ICP0 truncation mutants,

Indexed as

Herpesvirus 1, HumanImmediate-Early ProteinsInterferon Type IUbiquitin-Protein LigasesAmino AcidsAntiviral AgentsHumansLatent InfectionViral ProteinsAmino AcidsAntiviral AgentsImmediate-Early ProteinsInterferon Type IUbiquitin-Protein LigasesViral ProteinsVmw110 protein, Human herpesvirus 1E3 ubiquitin ligaseherpes simplex virusHSV-1ICP0innate immunityinterferon-betainterferonsviral gene expression

Identifiers

PMID35730940
PMCPMC9430112
OpenAlexW4283320036

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.