Rapid detection of Burkholderia glumae, causing panicle blight of rice, by colorimetric Loop-Mediated Isothermal Amplification (LAMP)

Bacterial panicle blight (BPB), caused by Burkholderia glumae, is an emerging threat to rice production, leading to significant yield losses. The seedborne nature of B. glumae amplifies its threat to seed production, transboundary movement and plant quarantine. Rapid detection and accurate identific...

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Autores principales: Catausan, Sheryl, Grande, Genelou, Schepler-Luu, Van, Castellion Martina
Formato: Póster
Lenguaje:Inglés
Publicado: International Rice Research Institute 2025
Materias:
Acceso en línea:https://hdl.handle.net/10568/178986
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author Catausan, Sheryl
Grande, Genelou
Schepler-Luu, Van
Castellion Martina
author_browse Castellion Martina
Catausan, Sheryl
Grande, Genelou
Schepler-Luu, Van
author_facet Catausan, Sheryl
Grande, Genelou
Schepler-Luu, Van
Castellion Martina
author_sort Catausan, Sheryl
collection Repository of Agricultural Research Outputs (CGSpace)
description Bacterial panicle blight (BPB), caused by Burkholderia glumae, is an emerging threat to rice production, leading to significant yield losses. The seedborne nature of B. glumae amplifies its threat to seed production, transboundary movement and plant quarantine. Rapid detection and accurate identification are critical in implementing effective containment measures and preventing the spread of the disease. However, existing diagnostic methods such as PCR and culture-based techniques using semi-selective medium are often complex, time consuming, and limited to well-equipped laboratories. This study aims to develop a rapid, cost-effective, and field-deployable detection method using loop-mediated isothermal amplification (LAMP). Unlike conventional PCR methods that require electrophoresis, LAMP results can be easily detected through turbidity, fluorescence, or color changes as in colorimetric LAMP (cLAMP), making it suitable for on-field diagnosis. Using primers designed based on the 16-23S rDNA ITS region of B. glumae, the cLAMP assay described here demonstrates high sensitivity and specificity, differentiating B. glumae strains from other common rice-infecting bacteria; and successfully detects B. glumae in DNA, cell cultures, and crude extracts of infected rice seeds, leaf sheath and panicle, with 105 CFU/ml and 0.1ng to 1pg DNA detection limit. The rapid, simple, and relatively low-cost detection of this method is particularly beneficial to laboratories in developing countries, where resources and equipment for sophisticated diagnostic testing are often limited.
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spelling CGSpace1789862025-12-19T02:00:19Z Rapid detection of Burkholderia glumae, causing panicle blight of rice, by colorimetric Loop-Mediated Isothermal Amplification (LAMP) Catausan, Sheryl Grande, Genelou Schepler-Luu, Van Castellion Martina panicles blight bacterial diseases rice polymerase chain reaction diagnosis LAMP Bacterial panicle blight (BPB), caused by Burkholderia glumae, is an emerging threat to rice production, leading to significant yield losses. The seedborne nature of B. glumae amplifies its threat to seed production, transboundary movement and plant quarantine. Rapid detection and accurate identification are critical in implementing effective containment measures and preventing the spread of the disease. However, existing diagnostic methods such as PCR and culture-based techniques using semi-selective medium are often complex, time consuming, and limited to well-equipped laboratories. This study aims to develop a rapid, cost-effective, and field-deployable detection method using loop-mediated isothermal amplification (LAMP). Unlike conventional PCR methods that require electrophoresis, LAMP results can be easily detected through turbidity, fluorescence, or color changes as in colorimetric LAMP (cLAMP), making it suitable for on-field diagnosis. Using primers designed based on the 16-23S rDNA ITS region of B. glumae, the cLAMP assay described here demonstrates high sensitivity and specificity, differentiating B. glumae strains from other common rice-infecting bacteria; and successfully detects B. glumae in DNA, cell cultures, and crude extracts of infected rice seeds, leaf sheath and panicle, with 105 CFU/ml and 0.1ng to 1pg DNA detection limit. The rapid, simple, and relatively low-cost detection of this method is particularly beneficial to laboratories in developing countries, where resources and equipment for sophisticated diagnostic testing are often limited. 2025 2025-12-18T05:55:00Z 2025-12-18T05:55:00Z Poster https://hdl.handle.net/10568/178986 en Open Access application/pdf International Rice Research Institute Catausan, Sheryl, Genelou Grande, Van Schepler-Luu, Martina Castellion (2025). Rapid detection of Burkholderia glumae, causing panicle blight of rice, by colorimetric Loop-Mediated Isothermal Amplification (LAMP). International Rice Research Institute. 1 p.
spellingShingle panicles
blight
bacterial diseases
rice
polymerase chain reaction
diagnosis
LAMP
Catausan, Sheryl
Grande, Genelou
Schepler-Luu, Van
Castellion Martina
Rapid detection of Burkholderia glumae, causing panicle blight of rice, by colorimetric Loop-Mediated Isothermal Amplification (LAMP)
title Rapid detection of Burkholderia glumae, causing panicle blight of rice, by colorimetric Loop-Mediated Isothermal Amplification (LAMP)
title_full Rapid detection of Burkholderia glumae, causing panicle blight of rice, by colorimetric Loop-Mediated Isothermal Amplification (LAMP)
title_fullStr Rapid detection of Burkholderia glumae, causing panicle blight of rice, by colorimetric Loop-Mediated Isothermal Amplification (LAMP)
title_full_unstemmed Rapid detection of Burkholderia glumae, causing panicle blight of rice, by colorimetric Loop-Mediated Isothermal Amplification (LAMP)
title_short Rapid detection of Burkholderia glumae, causing panicle blight of rice, by colorimetric Loop-Mediated Isothermal Amplification (LAMP)
title_sort rapid detection of burkholderia glumae causing panicle blight of rice by colorimetric loop mediated isothermal amplification lamp
topic panicles
blight
bacterial diseases
rice
polymerase chain reaction
diagnosis
LAMP
url https://hdl.handle.net/10568/178986
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