Please use this identifier to cite or link to this item: http://223.31.159.10:8080/jspui/handle/123456789/1432
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dc.contributor.authorChaliha, Chayanika-
dc.contributor.authorSrivastava, Richa-
dc.contributor.authorKalita, Eeshan-
dc.contributor.authorSahoo, Lingaraj-
dc.contributor.authorVerma, Praveen K.-
dc.date.accessioned2022-12-27T06:44:20Z-
dc.date.available2022-12-27T06:44:20Z-
dc.date.issued2023-
dc.identifier.citationWorld Journal of Microbiology and Biotechnology, 39(2): 52en_US
dc.identifier.issn1573-0972-
dc.identifier.issn0959-3993-
dc.identifier.otherhttps://doi.org/10.1007/s11274-022-03506-y-
dc.identifier.urihttps://link.springer.com/article/10.1007/s11274-022-03506-y-
dc.identifier.urihttp://223.31.159.10:8080/jspui/handle/123456789/1432-
dc.descriptionAccepted date: 20 December 2022en_US
dc.description.abstractThis 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 °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.en_US
dc.description.sponsorshipThe authors sincerely acknowledge Dr. Subhadeep Chatterjee, Head, Laboratory of Plant-Microbe Interactions, Centre for DNA Fingerprinting and Diagnostics, Hyderabad for his invaluable input in the preparation of the manuscript. The authors thank Ananda Tea Estate and Pathalipam Grant, Lakhimpur District, Assam, India, and Happy Valley Tea Estate, Darjeeling, West Bengal, India for providing the blister blight infected tea leaf samples used in the study. This work was supported by DBT, Govt. of India, Twinning Research Grant (Grant No. BT/427/NE/TBP/2013) to Tezpur University, Assam and NIPGR, New Delhi. Chayanika Chaliha would like to acknowledge DST, Govt. of India for her DST INSPIRE Fellowship (IF-150964).en_US
dc.language.isoen_USen_US
dc.publisherSpringer Nature Publishing AGen_US
dc.subjectBlister blighten_US
dc.subjectExobasidium vexansen_US
dc.subjectLoop-mediated isothermal amplificationen_US
dc.subjectRapid detectionen_US
dc.subjectRealAmpen_US
dc.titleRapid and precise detection of cryptic tea pathogen Exobasidium vexans: RealAmp validation of LAMP approachen_US
dc.typeArticleen_US
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