Evidence map›Paper›PMID 30836694›Full record

ArticleViruses2019

Deficient Incorporation of Rabies Virus Glycoprotein into Virions Enhances Virus-Induced Immune Evasion and Viral Pathogenicity.

Chunfu Li, Hongliang Zhang, Lina Ji, Xiao Wang, Yongjun Wen, Guangpeng Li, Zhen F Fu, Yang Yang

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.3field-weighted citation impact, top 24% 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

9 citing papers in PubMed, 18 citations in OpenAlex.

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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

8 authors at 3 institutions in 2 countries.

Chunfu LiThe State Key Laboratory of Reproductive Regulation and Breeding of Grassland Livestock, School of Life Sciences, Inner Mongolia University, Hohhot 010070, China. lcf52082@163.com.
Hongliang ZhangCollege of Veterinary Medicine, Inner Mongolia Agricultural University, Hohhot 010018, China. zhanghongliang001@126.com.ORCID 0000-0002-4184-896X
Lina JiThe State Key Laboratory of Reproductive Regulation and Breeding of Grassland Livestock, School of Life Sciences, Inner Mongolia University, Hohhot 010070, China. nn930817@163.com.
Xiao WangThe State Key Laboratory of Reproductive Regulation and Breeding of Grassland Livestock, School of Life Sciences, Inner Mongolia University, Hohhot 010070, China. wangxiao@life.imu.edu.cn.
Yongjun WenCollege of Veterinary Medicine, Inner Mongolia Agricultural University, Hohhot 010018, China. yongjunwen@126.com.
Guangpeng LiThe State Key Laboratory of Reproductive Regulation and Breeding of Grassland Livestock, School of Life Sciences, Inner Mongolia University, Hohhot 010070, China. imudwzx@163.com.
Zhen F FuDepartment of Pathology, College of Veterinary Medicine, University of Georgia, Athens, GA 30602, USA. zhenfu@uga.edu.
Yang YangThe State Key Laboratory of Reproductive Regulation and Breeding of Grassland Livestock, School of Life Sciences, Inner Mongolia University, Hohhot 010070, China. yang55797961@163.com.
Inner Mongolia University · CNInner Mongolia Agricultural University · CNUniversity of Georgia · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Previous studies have shown that wild-type (wt) rabies virus (RABV) evades the host immune response by restricting expression of glycoprotein (G), which blocks activation of dendritic cells (DCs) and induces production of virus-neutralizing antibodies (VNAs). In the present study, wt RABVs not only restricted G expression but also reduced incorporation of G into mature virions compared with laboratory-adapted viruses. A recombinant RABV expressing triple G was used to further determine whether G expression relates to incorporation. The recombinant virus showed higher expression and incorporation of G and activated more DCs than the virus that expressed a single copy of G. Removal of G from viruses using subtilisin or Dithiothreitol (DTT)/ Nonidet P-40 (NP40) almost completely abolishes DC activation and VNA production. Consequently, these G-depleted viruses cause lethal infection in mice. Thus, wt RABVs can subvert DC-induced antiviral immune response and maintain pathogenicity by decreasing G expression in infected cells and G incorporation into virions.

Indexed as

Immune EvasionAnimalsAntibodies, NeutralizingAntibodies, ViralAntigens, ViralCell Line, TumorDendritic CellsDisease Models, AnimalGlycoproteinsMiceMice, Inbred BALB CMice, Inbred C57BLRabies virusViral Envelope ProteinsVirionVirus ActivationAntibodies, NeutralizingAntibodies, ViralAntigens, Viralglycoprotein G, Rabies virusGlycoproteinsViral Envelope Proteinsdendritic cell activationglycoprotein incorporationimmune evasionlaboratory-attenuated rabies virusmembrane fusionrabies viruswild-type rabies virus

Identifiers

PMID30836694
PMCPMC6466124
OpenAlexW2919367027

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.