Evidence map›Paper›PMID 42259978›Full record

ArticleCurrent microbiology2026

High-Throughput Sequencing-Guided Development and Validation of an RT-dPCR Assay for Sensitive Detection of Lentinula edodes Spherical Virus in Shiitake Mushrooms.

Min-Jae Kim, Chae-Min Kang, In-Gyeong Kim, Rae-Dong Jeong

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Article in Current microbiology, 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

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

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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

4 authors.

Min-Jae Kim *Department of Applied Biology, Chonnam National University, Gwangju, 61185, Republic of Korea.
Chae-Min Kang *Department of Applied Biology, Chonnam National University, Gwangju, 61185, Republic of Korea.
In-Gyeong KimDepartment of Applied Biology, Chonnam National University, Gwangju, 61185, Republic of Korea.
Rae-Dong JeongDepartment of Applied Biology, Chonnam National University, Gwangju, 61185, Republic of Korea. jraed2@jnu.ac.kr.

Funding

Rural Development Administration, Republic of Korea RS-2025-02304903
6 · The paper itself

Abstract

Shiitake (Lentinula edodes) cultivation is often affected by virus-associated degeneration, necessitating sensitive and quantitative diagnostics. This study used high-throughput sequencing (HTS) as a preliminary screening approach to identify the major mycoviruses present in symptomatic samples and to guide target selection for assay development. HTS identified Lentinula edodes spherical virus (LeSV) together with other shiitake-associated mycoviruses, and LeSV was selected as the target for assay development. Based on these results, a nanoplate-based reverse transcription digital PCR (RT-ndPCR) assay was developed for LeSV. The assay demonstrated high analytical specificity, with no cross-reactivity with LeNSRV1 or LeV, and achieved approximately 10-fold higher detection than RT-qPCR. When applied to 30 field samples, RT-ndPCR detected LeSV in 100% (30/30) of samples compared with 86.7% (26/30) by RT-qPCR, identifying additional low-titer positives. These findings demonstrate that RT-ndPCR provides sensitive detection and absolute quantification of LeSV for shiitake surveillance and health certification.

Indexed as

Fungal VirusesHigh-Throughput Nucleotide SequencingReverse Transcriptase Polymerase Chain ReactionShiitake MushroomsRNA, ViralSensitivity and SpecificityRNA, Viral

Identifiers

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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.