4.5 Article

Rapid and precise detection of cryptic tea pathogen Exobasidium vexans: RealAmp validation of LAMP approach

Journal

Publisher

SPRINGER
DOI: 10.1007/s11274-022-03506-y

Keywords

Blister blight; Exobasidium vexans; Loop-mediated isothermal amplification; Rapid detection; RealAmp

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This study developed a real-time loop-mediated isothermal amplification (RealAmp) assay for the rapid detection of Exobasidium vexans, the pathogen causing blister blight disease in tea. The assay showed high specificity for E. vexans and was able to detect fluorescence signals in real-time, indicating the potential for field-based detection. The rapid and precise RealAmp assay could greatly contribute to the management of blister blight disease in tea.
This work embodies the development of a real time loop mediated isothermal amplification (RealAmp) assay for the rapid detection of the cryptic tea phytopathogen, Exobasidium vexans, the causal organism of blister blight disease. Due to the widespread popularity of tea as a beverage and the associated agro-economy, the rapid detection and management of the fast-spreading blister blight disease have been a longstanding necessity. Loop-mediated isothermal amplification (LAMP) primers were designed targeting the E. vexans ITS rDNA region and the reaction temperature was optimized at 62 degrees C with a 60 min reaction time. Amplification of the E. vexans isolates in the initial LAMP reactions was confirmed by both agarose gel electrophoresis and SYBR Green I dye based colour change visualization. The specificity of the LAMP primers for E. vexans was validated by negative testing of seven different phytopathogenic test fungi using LAMP and RealAmp assay. The positive findings in RealAmp assay for E. vexans strain were corroborated via detecting fluorescence signals in real-time. Further, the LAMP assays performed with gDNA isolated from infected tea leaves revealed positive amplification for the presence of E. vexans. The results demonstrate that this rapid and precise RealAmp assay has the potential to be applied for field-based detection of E. vexans in real-time.

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