Evidence map›Paper›PMID 42295471›Full record

ArticleArchives of virology2026

Identification and characterization of an endogenous pararetrovirus in Gentiana triflora plants.

Masamichi Isogai, Shunsuke Tezuka, Akira Abe, Yutaro Takamura, Hajime Yaegashi

Abstract read
In one paragraph

Article in Archives of virology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

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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

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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

5 authors.

Masamichi IsogaiPlant Pathology Laboratory, Faculty of Agriculture, Iwate University, 18-8, Ueda 3- chome, Morioka, Iwate, 020-8550, Japan. isogai@iwate-u.ac.jp.ORCID http://orcid.org/0000-0002-3095-6439
Shunsuke TezukaPlant Pathology Laboratory, Faculty of Agriculture, Iwate University, 18-8, Ueda 3- chome, Morioka, Iwate, 020-8550, Japan.
Akira AbeIwate Biotechnology Research Center, 22-174-4, Narita, Kitakami, Iwate, 024-0003, Japan.ORCID http://orcid.org/0000-0002-0344-2643
Yutaro TakamuraHachimantai City Floricultural R & D Center, 70, Kamasuda, Hachimantai, Iwate, 028- 7592, Japan.
Hajime YaegashiPlant Pathology Laboratory, Faculty of Agriculture, Iwate University, 18-8, Ueda 3- chome, Morioka, Iwate, 020-8550, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Deep sequencing and de novo assembly of small RNAs (sRNA analysis) provide a powerful approach to detect plant RNA and DNA viruses. Here, using sRNA analysis of Gentiana triflora (gentian) plants affected with kobu-sho disease, a serious disease of gentian, we found caulimovirus-like sequences, provisionally designated as gentian caulimovirus-like sequence (GCVS). Analysis of the complete nucleotide sequence indicated that GCVS is a novel virus with a genomic structure and organization typical of members of genus Caulimovirus (family Caulimoviridae). Based on Southern blot hybridization and rolling circle amplification analyses, GCVS seems to be integrated into the genomes of a wild gentian plant and three F₁ gentian cultivars and their respective parents and without any episomal viral forms in plants. Consistently, no episomal virus was detected in gentian plants with kobu-sho disease. To confirm GCVS integration in the gentian genome, we used a BLASTn analysis of the gentian draft genome (4,374 contigs; total: 3,657,985,820 nucleotides [nt]) using the GCVS sequence as a query and identified 1,929 GCVS-derived fragments (total: 3,116,680 nt) across 280 contigs. All fragments were shorter than the full-length GCVS genome (8,125 nt), and more than 90% were less than 4,000 nt long. Open reading frames in these fragments encoded proteins containing numerous amino acid substitutions and were frequently disrupted by premature stop codons. Collectively, these features indicate that GCVS represents a non-infectious endogenous pararetrovirus, defined as a pararetroviral sequence that has been integrated into the host genome and is no longer capable of autonomous replication or infection.

Indexed as

CaulimoviridaeCaulimovirusGentianaPlant DiseasesBase SequenceGenome, ViralHigh-Throughput Nucleotide SequencingPhylogeny

Identifiers

PMID42295471
PMCPMC13269303

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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.