Evidence map›Paper›PMID 28491824›Full record

ArticleFrontiers in cellular and infection microbiology2017

Rabies Virus Infection Induces Microtubule Depolymerization to Facilitate Viral RNA Synthesis by Upregulating HDAC6.

Jie Zan, Song Liu, Dong-Nan Sun, Kai-Kun Mo, Yan Yan, Juan Liu, Bo-Li Hu, Jin-Yan Gu, Min Liao, Ji-Yong Zhou

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

17 citing papers in PubMed, 30 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

10 authors at 3 institutions in 1 country.

Jie ZanKey Laboratory of Animal Virology of Ministry of Agriculture, Zhejiang UniversityHangzhou, China.
Song LiuKey Laboratory of Animal Virology of Ministry of Agriculture, Zhejiang UniversityHangzhou, China.
Dong-Nan SunKey Laboratory of Animal Virology of Ministry of Agriculture, Zhejiang UniversityHangzhou, China.
Kai-Kun MoKey Laboratory of Animal Virology of Ministry of Agriculture, Zhejiang UniversityHangzhou, China.
Yan YanKey Laboratory of Animal Virology of Ministry of Agriculture, Zhejiang UniversityHangzhou, China.
Juan LiuKey Laboratory of Animal Virology of Ministry of Agriculture, Zhejiang UniversityHangzhou, China.
Bo-Li HuInstitute of Immunology, Nanjing Agricultural UniversityNanjing, China.
Jin-Yan GuCollaborative Innovation Center and State Key Laboratory for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, Zhejiang UniversityHangzhou, China.
Min LiaoKey Laboratory of Animal Virology of Ministry of Agriculture, Zhejiang UniversityHangzhou, China.
Ji-Yong ZhouKey Laboratory of Animal Virology of Ministry of Agriculture, Zhejiang UniversityHangzhou, China.
Zhejiang University · CNFirst Affiliated Hospital Zhejiang University · CNNanjing Agricultural University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rabies virus (RABV) is the cause of rabies, and is associated with severe neurological symptoms, high mortality rate, and a serious threat to human health. Although cellular tubulin has recently been identified to be incorporated into RABV particles, the effects of RABV infection on the microtubule cytoskeleton remain poorly understood. In this study, we show that RABV infection induces microtubule depolymerization as observed by confocal microscopy, which is closely associated with the formation of the filamentous network of the RABV M protein. Depolymerization of microtubules significantly increases viral RNA synthesis, while the polymerization of microtubules notably inhibits viral RNA synthesis and prevents the viral M protein from inducing the formation of the filamentous network. Furthermore, the histone deacetylase 6 (HDAC6) expression level progressively increases during RABV infection, and the inhibition of HDAC6 deacetylase activity significantly decreases viral RNA synthesis. In addition, the expression of viral M protein alone was found to significantly upregulate HDAC6 expression, leading to a substantial reduction in its substrate, acetylated α-tubulin, eventually resulting in microtubule depolymerization. These results demonstrate that HDAC6 plays a positive role in viral transcription and replication by inducing microtubule depolymerization during RABV infection.

Indexed as

Up-RegulationAcetylationAnimalsCell LineCell SurvivalCricetinaeCytoskeletonDimethyl SulfoxideGene Expression Regulation, ViralHEK293 CellsHistone Deacetylase 6HumansMiceMicroscopy, ConfocalMicrotubulesNucleic Acid Synthesis InhibitorsDimethyl SulfoxideHistone Deacetylase 6Nucleic Acid Synthesis InhibitorsPaclitaxelRNA, ViralTubulinViral Matrix Proteinsacetylated modificationmatrix proteinmicrotubule depolymerizationrabies virusviral RNA synthesis

Identifiers

PMID28491824
PMCPMC5405082
OpenAlexW2607936681

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.