Evidence map›Paper›PMID 42198730›Full record

ArticleViruses2026

Enterovirus Testing in Hand, Foot, and Mouth Disease and Herpangina: A Highly Sensitive Single-Round VP4-VP2 Reverse-Transcription Polymerase Chain Reaction Assay with a Redesigned Reverse Primer.

Tsuguto Fujimoto, Miki Ogi, Kazuhiro Kitakawa, Takako Sano, Yorihiro Nishimura, Kouichi Kitamura, Minami Kikuchi Ueno, Minetaro Arita

Abstract read
In one paragraph

Article in Viruses, 2026. 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
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

8 authors.

Tsuguto FujimotoDepartment of Fungal Infection, National Institute of Infectious Diseases, Japan Institute for Health Security (JIHS), Tokyo 162-8640, Japan.ORCID 0000-0002-4861-4349
Miki OgiInfectious Disease Research Division, Hyogo Prefectural Institute of Public Health Science, Kakogawa 675-0003, Japan.ORCID 0009-0005-5125-4240
Kazuhiro KitakawaFukushima Prefectural Institute for Public Health, Fukushima 960-8560, Japan.ORCID 0000-0001-6967-348X
Takako SanoMicrobiology Division, Kanagawa Prefectural Institute of Public Health, Chigasaki 253-0087, Japan.ORCID 0009-0009-2575-4902
Yorihiro NishimuraDepartment of Virology II, National Institute of Infectious Diseases, Japan Institute for Health Security (JIHS), Tokyo 208-0011, Japan.ORCID 0009-0007-7561-8509
Kouichi KitamuraDepartment of Virology II, National Institute of Infectious Diseases, Japan Institute for Health Security (JIHS), Tokyo 208-0011, Japan.ORCID 0000-0001-9692-8724
Minami Kikuchi UenoDepartment of Virology II, National Institute of Infectious Diseases, Japan Institute for Health Security (JIHS), Tokyo 208-0011, Japan.ORCID 0000-0001-5852-8738
Minetaro AritaDepartment of Virology II, National Institute of Infectious Diseases, Japan Institute for Health Security (JIHS), Tokyo 208-0011, Japan.ORCID 0000-0002-3314-6626

Funding

Japan Agency for Medical Research and Development JP24fk0108627 and JP25fk0108716
6 · The paper itself

Abstract

Molecular typing of enteroviruses (EVs) is essential for surveillance of hand, foot, and mouth disease (HFMD). Conventional reverse-transcription polymerase chain reaction (RT-PCR) targeting the VP4-VP2 region can be insufficiently sensitive, reducing the detectability of Enterovirus A (EV-A). We developed a single-round RT-PCR assay using a modified reverse primer design (C3R) for rapid EV detection and genotyping. Sensitivity was evaluated using EV-A71 and poliovirus type 1 reference strains, across 60 EV-positive clinical specimens. The C3R-based assay showed ~1000-fold higher sensitivity for EV-A71 than for conventional assays (limit of detection: 6.6 copies/reaction). The assay detected 98.3% (59/60) of clinical specimens in a single-round format, whereas the conventional assay detected only 45.0% (27/60) and showed a marked decline in detection at higher Ct values. The C3R-based assay maintained complete detection for clinical specimens with Ct values below 40. The majority of the amplified products yielded high-quality sequences suitable for genotyping. This C3R-based RT-PCR overcomes sensitivity limitations of existing protocols and provides reliable genotyping from low-viral-load specimens, supporting its use in routine diagnostics and large-scale HFMD surveillance.

Indexed as

DNA PrimersEnterovirusHand, Foot and Mouth DiseaseHerpanginaComputer SimulationGenotypeHumansLimit of DetectionReverse Transcriptase Polymerase Chain ReactionRNA, ViralSensitivity and SpecificityDNA PrimersRNA, Viraland mouth diseaseenterovirusfoothandherpanginareverse-transcription polymerase chain reaction

Identifiers

PMID42198730
PMCPMC13211326

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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.