Evidence map›Paper›PMID 37991369›Full record

ArticleJournal of virology2023

Shared sequence characteristics identified in non-canonical rearrangements of HSV-1 genomes.

Alina Shitrit, Valerya Nisnevich, Nofar Rozenshtein, Hila Kobo, Hoang Van Phan, Savaş Tay, Moriah Szpara, Matthew D Weitzman, Nir Drayman, Oren Kobiler

Open access · hybridAbstract read
In one paragraph

Article in Journal of virology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.7field-weighted citation impact, top 14% 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

8 citing papers in PubMed, 8 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 5 institutions in 2 countries.

Alina ShitritDepartment of Clinical Microbiology and Immunology, School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Valerya NisnevichDepartment of Clinical Microbiology and Immunology, School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Nofar RozenshteinDepartment of Clinical Microbiology and Immunology, School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Hila KoboGenomic Research Unit, Faculty of Life Science, Tel Aviv University, Tel Aviv, Israel.
Hoang Van PhanPritzker School of Molecular Engineering, University of Chicago, Chicago, Illinois, USA.
Savaş TayPritzker School of Molecular Engineering, University of Chicago, Chicago, Illinois, USA.
Moriah SzparaDepartment of Biochemistry and Molecular Biology, Department of Biology, Center for Infectious Disease Dynamics, and the Huck Institutes of the Life Sciences, Pennsylvania State University, University Park, Pennsylvania, USA.ORCID 0000-0001-9859-1678
Matthew D WeitzmanDivision of Protective Immunity, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.ORCID 0000-0001-9713-167X
Nir DraymanDepartment of Molecular Biology and Biochemistry, School of Biological Sciences, University of California, Irvine, California, USA.
Oren KobilerDepartment of Clinical Microbiology and Immunology, School of Medicine, Tel Aviv University, Tel Aviv, Israel.ORCID 0000-0001-9914-3770
Tel Aviv University · ILUniversity of Chicago · USChildren's Hospital of Philadelphia · USPennsylvania State University · USUniversity of California, Irvine · US

Funding

The impact of viral genomic variation on neonatal disease outcomesR01AI163217 · NIAID · PENNSYLVANIA STATE UNIVERSITY, THE · PI MORIAH SZPARA · 2022 to 2026
$3.2M
Israel Science Foundation (ISF) Grant 1816/21NIAID NIH HHS R01 AI163217United States - Israel Binational Science Foundation (BSF) Grant 2019331
6 · The paper itself

Abstract

importanceMutations and genetic rearrangements are the primary driving forces of evolution. Viruses provide valuable model systems for investigating these mechanisms due to their rapid evolutionary rates and vast genetic variability. To investigate genetic rearrangements in the double-stranded DNA genome of herpes simplex virus type 1, the viral population was serially passaged in various cell types. The serial passaging led to formation of defective genomes, resulted from cell-specific non-canonical rearrangements (NCRs). Interestingly, we discovered shared sequence characteristics underlying the formation of these NCRs across all cell types. Moreover, most NCRs identified in clinical samples shared these characteristics. Based on our findings, we propose a model elucidating the formation of NCRs during viral replication within the nucleus of eukaryotic cells.

Indexed as

DNA, ViralGenome, ViralHerpesvirus 1, HumanMutationCell NucleusEukaryotic CellsHumansSerial PassageVirus ReplicationDNA, Viraldefective interfering particlesDNA rearrangementsherpesvirusesmicrohomology

Identifiers

PMID37991369
PMCPMC10734421
OpenAlexW4388901774

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.