Evidence map›Paper›PMID 36072891›Full record

ArticleBiochemistry and biophysics reports2022

Independent evolution of multi-dominant viral genome species observed in a hepatitis C virus carrier.

Tomomi Ando, Hideki Aizaki, Masaya Sugiyama, Tomoko Date, Kazuhiko Hayashi, Masatoshi Ishigami, Yoshiaki Katano, Hidemi Goto, Masashi Mizokami, Masamichi Muramatsu and 2 more

Abstract read
In one paragraph

Article in Biochemistry and biophysics reports, 2022. 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
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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.

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

12 authors.

Tomomi AndoDepartment of Virology II, National Institute of Infectious Diseases, Tokyo, Japan.
Hideki AizakiDepartment of Virology II, National Institute of Infectious Diseases, Tokyo, Japan.
Masaya SugiyamaDepartment of Viral Pathogenesis and Controls, National Center for Global Health and Medicine, Chiba, Japan.
Tomoko DateGenome Medical Science Project, National Center for Global Health and Medicine, Chiba, Japan.
Kazuhiko HayashiDepartment of Gastroenterology and Hepatology, Federation of National Public Service Personnel Mutual Aid Associations, Meijo Hospital, Nagoya, Japan.
Masatoshi IshigamiDepartment of Gastroenterology and Hepatology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Yoshiaki KatanoDepartment of Gastroenterology, Bantane Hospital, Fujita Health University School of Medicine, Nagoya, Japan.
Hidemi GotoDepartment of Gastroenterology and Hepatology, Federation of National Public Service Personnel Mutual Aid Associations, Meijo Hospital, Nagoya, Japan.
Masashi MizokamiGenome Medical Science Project, National Center for Global Health and Medicine, Chiba, Japan.
Masamichi MuramatsuDepartment of Virology II, National Institute of Infectious Diseases, Tokyo, Japan.
Makoto KurodaPathogen Genomics Center, National Institute of Infectious Diseases, Tokyo, Japan.
Takaji WakitaDepartment of Virology II, National Institute of Infectious Diseases, Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The viral genome quasispecies composition of hepatitis C virus (HCV) could have important implications to viral pathogenesis and resistance to anti-viral treatment. The purpose of the present study was to profile the HCV RNA quasispecies. We developed a strategy to determine the full-length HCV genome sequences co-existing within a single patient serum by using next-generation sequencing technologies. The isolated viral clones were divided into the groups that can be distinguished by core amino acid 70 substitution. Subsequently, we determined HCV full-length genome sequences of three independent dominant species co-existing in the sequential serum with a 7-year interval. From phylogenetic analysis, these dominant species evolved independently. Our study demonstrated that multiple dominant species co-existed in patient sera and evolved independently.

Indexed as

Core 70 polymorphismcore70, the core amino acid 70 substitutionsE, envelopeHCVHVR, hyper variable regionIRRDR, IFN and ribavirin resistance-determining regionISDR, IFN sensitivity-determining regionNext-generation sequencingNGS, next-generation sequencingNS, nonstructuralPEG-IFN, pegylated interferonQ, glutamineQuasispeciesR, arginineRBV, ribavirinSVR, sustained virological response

Identifiers

PMID36072891
PMCPMC9441305

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Registered trials

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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.