Evidence map›Paper›PMID 28827540›Full record

ArticleScientific reports2017

The Us2 Gene Product of Herpes Simplex Virus 2 modulates NF-κB activation by targeting TAK1.

Xuan Lu, Changjing Huang, Yi Zhang, Yong Lin, Xueyu Wang, Qian Li, Shi Liu, Jingfeng Tang, Li Zhou

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

12 citing papers in PubMed, 14 citations in OpenAlex.

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  8. The Peptide A-3302-B Isolated from a Marine BacteriumInternational journal of molecular sciences · 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 2 countries.

Xuan LuDepartment of Medical Genetics, Wuhan University School of Basic Medical Sciences, Wuhan, 430072, China.
Changjing HuangCollege of Biological Engineering and Food Sciences, Hubei University of Technology, Wuhan, 430068, China.
Yi ZhangCollege of Biological Engineering and Food Sciences, Hubei University of Technology, Wuhan, 430068, China.
Yong LinInstitute of Virology, University Hospital of Essen, University of Duisburg-Essen, Essen, 45122, Germany.
Xueyu WangInstitute of Virology, University Hospital of Essen, University of Duisburg-Essen, Essen, 45122, Germany.
Qian LiInstitute of Virology, University Hospital of Essen, University of Duisburg-Essen, Essen, 45122, Germany.
Shi LiuState Key Laboratory of Virology, College of Life Sciences, Wuhan University, Wuhan, 430071, China.
Jingfeng TangCollege of Biological Engineering and Food Sciences, Hubei University of Technology, Wuhan, 430068, China.
Li ZhouAnimal Biosafety Level III Laboratory at the Center for Animal Experiment, Wuhan University School of Medicine, Wuhan, 430072, China. zhouli_jerry@whu.edu.cn.
Hubei University of Technology · CNUniversity of Duisburg-Essen · DEWuhan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

HSV-2 is one of the most common sexually transmitted pathogens worldwide and HSV-2 infection triggers cytokine and chemokine production. However, little is known about which HSV-2 genes engage in the regulation of NF-κB signaling and what mechanisms are involved. In a screen of the unique short (Us) regions of HSV-2, we observed that HSV-2 Us2 activates NF-κB signaling. We additionally indicated that deficiencies of Us2 decrease HSV-2 WT mediated NF-κB activation and cytokine and chemokine production, and overexpression of Us2 showed opposite effects. Co-immunoprecipitations indicated that Us2 interacted with TGF-β activated kinase 1 (TAK1), a serine/threonine kinase essential for NF-κB activation, and Us2 has the ability to regulate the TAK1-mediated pathway and induces TAK1 downstream signaling. Further studies verified that Us2 induced the phosphorylation of TAK1, resulting in the activation of TAK1 mediated downstream signaling. The role of Us2 in HSV-2 induced NF-κB pathways was also confirmed in the Us2-deficient mutant and HSV-2 WT infected mice. Our results indicate that HSV-2 Us2 gene product binds to TAK1 to positively regulate NF-κB signaling and, for the first time, provide insights into the molecular mechanism.

Indexed as

Host-Pathogen InteractionsAnimalsCell LineDisease Models, AnimalFemaleHerpes GenitalisHerpesvirus 2, HumanHumansImmunoprecipitationMAP Kinase Kinase Kinase 7MAP Kinase Kinase KinasesMice, Inbred BALB CNF-kappa B p50 SubunitProtein BindingProtein Interaction MappingViral Envelope ProteinsMAP Kinase Kinase Kinase 7MAP Kinase Kinase KinasesNF-kappa B p50 SubunitNfkb1 protein, mouseUS2 protein, herpes simplex virus 2Viral Envelope Proteins

Identifiers

PMID28827540
PMCPMC5566419
OpenAlexW2742683883

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.