Evidence map›Paper›PMID 30728265›Full record

ArticleJournal of virology2019

Generation of Infectious Recombinant Human Rotaviruses from Just 11 Cloned cDNAs Encoding the Rotavirus Genome.

Satoshi Komoto, Saori Fukuda, Masanori Kugita, Riona Hatazawa, Chitose Koyama, Kazuhiko Katayama, Takayuki Murata, Koki Taniguchi

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 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
4.6field-weighted citation impact, top 4% 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

33 citing papers in PubMed, 52 citations in OpenAlex.

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  12. Recurrent viral capture of cellular phosphodiesterases that antagonize OAS-RNase L.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  13. Recovery of Recombinant Rotaviruses by Reverse Genetics.Methods in molecular biology (Clifton, N.J.) · 2024
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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 1 institution in 1 country.

Satoshi Komoto *Department of Virology and Parasitology, Fujita Health University School of Medicine, Toyoake, Aichi, Japan satoshik@fujita-hu.ac.jp.ORCID 0000-0003-2810-8163
Saori Fukuda *Department of Virology and Parasitology, Fujita Health University School of Medicine, Toyoake, Aichi, Japan.
Masanori KugitaDepartment of Virology and Parasitology, Fujita Health University School of Medicine, Toyoake, Aichi, Japan.
Riona HatazawaDepartment of Virology and Parasitology, Fujita Health University School of Medicine, Toyoake, Aichi, Japan.
Chitose KoyamaLaboratory of Viral Infection I, Kitasato Institute for Life Sciences, Graduate School of Infection Control Sciences, Tokyo, Japan.
Kazuhiko KatayamaLaboratory of Viral Infection I, Kitasato Institute for Life Sciences, Graduate School of Infection Control Sciences, Tokyo, Japan.
Takayuki MurataDepartment of Virology and Parasitology, Fujita Health University School of Medicine, Toyoake, Aichi, Japan.
Koki TaniguchiDepartment of Virology and Parasitology, Fujita Health University School of Medicine, Toyoake, Aichi, Japan.
Fujita Health University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The generation of recombinant group A rotaviruses (RVAs) entirely from cloned cDNAs has been described only for a single animal RVA strain, simian SA11-L2. We recently developed an optimized RVA reverse genetics system based on only RVA cDNAs (11-plasmid system), in which the concentration of cDNA plasmids containing the NSP2 and NSP5 genes is 3- or 5-fold increased in relation to that of the other plasmids. Based on this approach, we generated a recombinant human RVA (HuRVA)-based monoreassortant virus containing the VP4 gene of the simian SA11-L2 virus using the 11-plasmid system. In addition to this monoreassortant virus, authentic HuRVA (strain KU) was also generated with the 11-plasmid system with some modifications. Our results demonstrate that the 11-plasmid system involving just RVA cDNAs can be used for the generation of recombinant HuRVA and recombinant HuRVA-based reassortant viruses.

Indexed as

Cloning, MolecularGenome, ViralRotavirusViral Nonstructural ProteinsAnimalsCell LineCricetinaeDNA, ComplementaryHumansPlasmidsDNA, ComplementaryNSP5 protein, rotavirus group AViral Nonstructural Proteins11-plasmid systemhuman rotavirusreassortmentreverse genetics

Identifiers

PMID30728265
PMCPMC6450123
OpenAlexW2912199523

What OpenQuestion holds

Textmetadata
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.