Evidence map›Paper›PMID 42092612›Full record

ArticleVirus research2026

Improved detection of rice yellow mottle virus with a polyclonal antibody xMAP assay: A high-throughput alternative to ELISA.

A Vernet, G Thaurignac, N Poulicard, J Bouillin, A Pinel-Galzi, A Pinault, P K A Bamogo, M Peeters, A Ayouba, S Lacombe

Abstract readEvaluation Study
In one paragraph

Article in Virus research, 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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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

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5 · Who and what money

Authors and funding

10 authors.

A VernetPHIM, Plant Health Institute of Montpellier, Univ. Montpellier, IRD, CIRAD, INRAE, Institute Agro, Montpellier, France.
G ThaurignacTransVIHMI, Univ. Montpellier, IRD UMI 233, Inserm U1175, Montpellier, 34090, France.
N PoulicardPHIM, Plant Health Institute of Montpellier, Univ. Montpellier, IRD, CIRAD, INRAE, Institute Agro, Montpellier, France.
J BouillinTransVIHMI, Univ. Montpellier, IRD UMI 233, Inserm U1175, Montpellier, 34090, France.
A Pinel-GalziPHIM, Plant Health Institute of Montpellier, Univ. Montpellier, IRD, CIRAD, INRAE, Institute Agro, Montpellier, France.
A PinaultPHIM, Plant Health Institute of Montpellier, Univ. Montpellier, IRD, CIRAD, INRAE, Institute Agro, Montpellier, France.
P K A BamogoPHIM, Plant Health Institute of Montpellier, Univ. Montpellier, IRD, CIRAD, INRAE, Institute Agro, Montpellier, France.
M PeetersTransVIHMI, Univ. Montpellier, IRD UMI 233, Inserm U1175, Montpellier, 34090, France.
A AyoubaPHIM, Plant Health Institute of Montpellier, Univ. Montpellier, IRD, CIRAD, INRAE, Institute Agro, Montpellier, France.
S LacombePHIM, Plant Health Institute of Montpellier, Univ. Montpellier, IRD, CIRAD, INRAE, Institute Agro, Montpellier, France. Electronic address: severine.lacombe@ird.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rice yellow mottle virus (RYMV) is one of the most destructive viral pathogens affecting rice production in sub-Saharan Africa, where its extensive genetic diversity and high evolutionary rate complicate reliable diagnosis. Current serological methods, notably double-antibody sandwich enzyme-linked immunosorbent assay (DAS-ELISA), are widely used for routine detection but may lack sensitivity when viral loads are low or samples are degraded. In this study, we developed and evaluated a high-throughput microsphere immunoassay (MIA) based on Luminex xMAP technology as an alternative serological tool for RYMV detection. A panel of three monoclonal antibodies (mABs) and one polyclonal antibody (pAB), all raised against a RYMV isolate from Madagascar, was assessed using greenhouse-propagated and field-collected rice samples representing all six known RYMV genetic groups. Assay performance was evaluated in terms of sensitivity, specificity, and accuracy using receiver operating characteristic (ROC) curve analysis, and results were compared with those obtained by DAS-ELISA. While mABs failed to retain their expected serotype specificity in the xMAP format, the polyclonal antibody enabled robust and strain-independent detection of RYMV. The pAB-based xMAP assay showed excellent diagnostic performance, with 100% specificity, sensitivity exceeding 97%, and an area under the ROC curve of 0.99. Importantly, the pAB-based xMAP assay demonstrated a 100- to 500-fold increase in sensitivity compared with DAS-ELISA, allowing reliable detection of RYMV in samples with low viral loads or compromised integrity. No cross-reactivity was observed with other co-circulating rice viruses, including maize streak virus and rice stripe necrosis virus. This study demonstrates that a polyclonal antibody-based xMAP immunoassay provides a highly sensitive, specific, and scalable alternative to conventional ELISA for RYMV diagnosis. This approach represents a promising tool for large-scale epidemiological surveys and improved management of rice viral diseases in Africa.

Indexed as

Antibodies, ViralHigh-Throughput Screening AssaysOryzaPlant DiseasesPlant VirusesAntibodies, MonoclonalEnzyme-Linked Immunosorbent AssayImmunoassayROC CurveSensitivity and SpecificityAntibodies, MonoclonalAntibodies, ViralDiagnosticPolyclonal antibodyRYMVxMAP Luminex immunoassay

Identifiers

PMID42092612
PMCPMC13195790

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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.