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dc.contributor.authorKumar, A-
dc.contributor.authorSARMA, Y R-
dc.contributor.authorPriou, S-
dc.date.accessioned2018-01-02T06:39:25Z-
dc.date.available2018-01-02T06:39:25Z-
dc.date.issued2002-
dc.identifier.citationJournal of Spices and Aromatic Crops, Vol.11, No.1, pp.35-40, 2002en_US
dc.identifier.urihttp://hdl.handle.net/123456789/1172-
dc.description.abstractBacterial wilt, caused by Ralstonia solanacearum, is an important production constraint in ginger.The pathogen is seed rhizome borne and the low level of inoculums is very difficult to be detected and monitored by conventional methods. Pathogen detection and selection of healthy planting materials is an important prerequisite for the production of a healthy crop of ginger in the field. In the present work we have evaluated the suitability of NCM-ELISA kit, developed at international Potato Center(CIP), Lima, Peru, for detecting bacterial wilt pathogen in ginger. The result indicated that the antibodies developed at CIP for potato strain of R. solanacearum was sensitive enough to detect R. solanacearum from ginger, chilli, Chromolaena and tomato. The sensitivity of the kit was determined to be 42cells per ml of ginger extract when ELISA was performed after enrichment in selecyive medium. We have also tested the specificity of antibodies and found that the antibodies were specific for R. solanacearum. The extraction protocol (citrate buffer at PH 5.6) developed for potato was found to be suitable for ginger also.en_US
dc.subjectBacterial wilten_US
dc.subjectgingeren_US
dc.subjectNCM-ELISAen_US
dc.subjectRalstonia solanacearumen_US
dc.subjectrhizome borne diseaseen_US
dc.titleDetection of Ralstonia solanacearum in ginger rhizomes using post-enrichment NCM-ELISAen_US
dc.typeArticleen_US
Appears in Collections:CROP PROTECTION

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