Evidence map›Paper›PMID 30651355›Full record

ArticleJournal of virology2019

Cryo-electron Microscopy Structures of Novel Viruses from Mud Crab

Yuanzhu Gao, Shanshan Liu, Jiamiao Huang, Qianqian Wang, Kunpeng Li, Jian He, Jianguo He, Shaoping Weng, Qinfen Zhang

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

4 citing papers in PubMed, 19 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

9 authors at 1 institution in 1 country.

Yuanzhu Gao *State Key Lab for Biocontrol, School of Life Sciences, Sun Yat-sen University, Guangzhou, China.
Shanshan Liu *State Key Lab for Biocontrol, School of Life Sciences, Sun Yat-sen University, Guangzhou, China.
Jiamiao Huang *State Key Lab for Biocontrol, School of Life Sciences, Sun Yat-sen University, Guangzhou, China.
Qianqian WangState Key Lab for Biocontrol, School of Life Sciences, Sun Yat-sen University, Guangzhou, China.
Kunpeng LiState Key Lab for Biocontrol, School of Life Sciences, Sun Yat-sen University, Guangzhou, China.
Jian HeJoint Experimental Teaching Center, Sun Yat-sen University, Guangzhou, China.
Jianguo HeState Key Lab for Biocontrol, School of Life Sciences, Sun Yat-sen University, Guangzhou, China.
Shaoping WengState Key Lab for Biocontrol, School of Life Sciences, Sun Yat-sen University, Guangzhou, China Lsswsp@mail.sysu.edu.cn Lsszqf@mail.sysu.edu.cn.
Qinfen ZhangState Key Lab for Biocontrol, School of Life Sciences, Sun Yat-sen University, Guangzhou, China Lsswsp@mail.sysu.edu.cn Lsszqf@mail.sysu.edu.cn.
Sun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Viruses associated with sleeping disease (SD) in crabs cause great economic losses to aquaculture, and no effective measures are available for their prevention. In this study, to help develop novel antiviral strategies, single-particle cryo-electron microscopy was applied to investigate viruses associated with SD. The results not only revealed the structure of mud crab dicistrovirus (MCDV) but also identified a novel mud crab tombus-like virus (MCTV) not previously detected using molecular biology methods. The structure of MCDV at a 3.5-Å resolution reveals three major capsid proteins (VP1 to VP3) organized into a pseudo-T=3 icosahedral capsid, and affirms the existence of VP4. Unusually, MCDV VP3 contains a long C-terminal region and forms a novel protrusion that has not been observed in other dicistrovirus. Our results also reveal that MCDV can release its genome via conformation changes of the protrusions when viral mixtures are heated. The structure of MCTV at a 3.3-Å resolution reveals a T= 3 icosahedral capsid with common features of both tombusviruses and nodaviruses. Furthermore, MCTV has a novel hydrophobic tunnel beneath the 5-fold vertex and 30 dimeric protrusions composed of the P-domains of the capsid protein at the 2-fold axes that are exposed on the virion surface. The structural features of MCTV are consistent with a novel type of virus.

Indexed as

AnimalsBrachyuraCapsidCapsid ProteinsCryoelectron MicroscopyDicistroviridaeViral Structural ProteinsVirionVirus DiseasesCapsid ProteinsViral Structural Proteinscryo-EMvirion structurevirus

Identifiers

PMID30651355
PMCPMC6430526
OpenAlexW3006969943

What OpenQuestion holds

Textmetadata
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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.