Duplex real‐time PCR for routine detection of Pantoea stewartii subsp. stewartii in maize seeds

Fuente: Wiley Open Access
Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Léa Casagrande, Luis Buendia, Laurent Kamel
Format: Artículo Open Access
Veröffentlicht: Wiley 2026
Schlagworte:
Online-Zugang:
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
_version_ 1867010168808538112
author Léa Casagrande
Luis Buendia
Laurent Kamel
author_facet Léa Casagrande
Luis Buendia
Laurent Kamel
Léa Casagrande
Luis Buendia
Laurent Kamel
collection Wiley Open Access
contents Duplex real‐time PCR for routine detection of Pantoea stewartii subsp. stewartii in maize seeds Léa Casagrande Luis Buendia Laurent Kamel EPPO Bulletin Abstract Pantoea stewartii subsp. stewartii is a phytopathogenic bacterium affecting maize, responsible for Stewart's wilt and leaf scorch along the veins. Native to North America and seed‐transmitted, this species is considered a quarantine pest and is under enhanced surveillance within the European Union. Despite the implementation of phytosanitary measures, no sufficiently reliable detection test is currently available. Existing tests—based on antigen recognition (ELISA) or DNA detection (PCR)—often fail to differentiate this pathogen from closely related subspecies, leading to false‐positive results. Recent studies have identified specific PCR primer sets that improve the specificity of P. stewartii subsp. stewartii detection. Building upon these findings, we present a diagnostic protocol on maize seeds using a quantitative duplex real‐time PCR test suitable for routine laboratory testing. The primer pair cpsAB2313F/cpsR was selected for specific detection of Pantoea stewartii subsp. stewartii , while the primer pair Wu‐F/Wu‐R was used as an internal amplification control. The test was able to detect a single P. stewartii subsp. stewartii contaminated seed within a subsample of 2000 healthy seeds but had only 83.3% repeatability with one contaminated seed in a subsample of 1000 seeds. Therefore, one contaminated seed in a subsample of 400 seeds was set as the detection limit. This batch size is suitable for routine seed testing programs. 10.1111/epp.70047 http://onlinelibrary.wiley.com/termsAndConditions#vor
doi_str_mv 10.1111/epp.70047
format Artículo Open Access
id wiley_oa_10_1111_epp_70047
institution Wiley Open Access
license_str_mv http://onlinelibrary.wiley.com/termsAndConditions#vor
publishDate 2026
publisher Wiley
record_format wiley_oa
spellingShingle Duplex real‐time PCR for routine detection of Pantoea stewartii subsp. stewartii in maize seeds
Léa Casagrande
Luis Buendia
Laurent Kamel
EPPO Bulletin
Duplex real‐time PCR for routine detection of Pantoea stewartii subsp. stewartii in maize seeds Léa Casagrande Luis Buendia Laurent Kamel EPPO Bulletin Abstract Pantoea stewartii subsp. stewartii is a phytopathogenic bacterium affecting maize, responsible for Stewart's wilt and leaf scorch along the veins. Native to North America and seed‐transmitted, this species is considered a quarantine pest and is under enhanced surveillance within the European Union. Despite the implementation of phytosanitary measures, no sufficiently reliable detection test is currently available. Existing tests—based on antigen recognition (ELISA) or DNA detection (PCR)—often fail to differentiate this pathogen from closely related subspecies, leading to false‐positive results. Recent studies have identified specific PCR primer sets that improve the specificity of P. stewartii subsp. stewartii detection. Building upon these findings, we present a diagnostic protocol on maize seeds using a quantitative duplex real‐time PCR test suitable for routine laboratory testing. The primer pair cpsAB2313F/cpsR was selected for specific detection of Pantoea stewartii subsp. stewartii , while the primer pair Wu‐F/Wu‐R was used as an internal amplification control. The test was able to detect a single P. stewartii subsp. stewartii contaminated seed within a subsample of 2000 healthy seeds but had only 83.3% repeatability with one contaminated seed in a subsample of 1000 seeds. Therefore, one contaminated seed in a subsample of 400 seeds was set as the detection limit. This batch size is suitable for routine seed testing programs. 10.1111/epp.70047 http://onlinelibrary.wiley.com/termsAndConditions#vor
title Duplex real‐time PCR for routine detection of Pantoea stewartii subsp. stewartii in maize seeds
topic EPPO Bulletin
url https://onlinelibrary.wiley.com/doi/10.1111/epp.70047