Evidence map›Paper›PMID 37405556›Full record

ArticleVirus genes2023

Whole genome sequencing and genomic characterization of a DS-1-like G2P[4] group A rotavirus in Japan.

Tung Phan, Toshiyuki Hikita, Shoko Okitsu, Yuki Akari, Satoshi Komoto, Satoshi Hayakawa, Hiroshi Ushijima

Abstract read
PubMed Publisher
In one paragraph

Article in Virus genes, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 88% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

7 authors at 3 institutions in 2 countries.

Tung PhanDepartment of Pathology, University of Pittsburgh, Pittsburgh, PA, USA.
Toshiyuki HikitaHikita Pediatric Clinic, Kiryu, Gunma, Japan.
Shoko OkitsuDivision of Microbiology, Nihon University School of Medicine, Itabashi-ku, Tokyo, Japan.
Yuki AkariDepartment of Virology and Parasitology, Fujita Health University School of Medicine, Toyoake, Aichi, Japan.
Satoshi KomotoDepartment of Virology and Parasitology, Fujita Health University School of Medicine, Toyoake, Aichi, Japan.
Satoshi HayakawaDivision of Microbiology, Nihon University School of Medicine, Itabashi-ku, Tokyo, Japan.
Hiroshi UshijimaDivision of Microbiology, Nihon University School of Medicine, Itabashi-ku, Tokyo, Japan. ushijima-hiroshi@jcom.home.ne.jp.
Nihon University · JPFujita Health University · JPUniversity of Pittsburgh · US

Funding

Japan Agency for Medical Research and Development JP22fk01081222 and JP22wm0225006Japan Society for the Promotion of Science 16H05360 and 20K10455
6 · The paper itself

Abstract

After rotavirus was discovered in 1973, it became the leading pathogen in causing acute gastroenteritis in humans worldwide. In this study, we performed whole genome sequencing and genomic characterization of a DS-1-like G2P[4] group A rotavirus in feces of a Japanese child with acute gastroenteritis who was fully Rotarix® vaccinated. The genomic investigation determined a genomic constellation G2-P[4]-I2-R2-C2-M2-A2-N2-T2-E2-H2 of this rotavirus strain. Its antigenic epitopes of the VP7 and VP4 proteins had significant mismatches compared with the vaccine strains. Our study is the latest attempt to investigate the evolution of the VP7 and VP4 genes of emerging G2P[4] rotavirus in Japan.

Indexed as

GastroenteritisRotavirusRotavirus InfectionsChildGenome, ViralGenomicsGenotypeHumansJapanPhylogenyWhole Genome SequencingEvolutionG2P[4]JapanRotavirusWhole genome sequencing

Identifiers

PMID37405556
OpenAlexW4383186326

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.