Biological characterization of bud necrosis virus disease in watermelon(Citrullus lanatus T.)

dc.contributor.advisorVimi, Louis (Guide)
dc.contributor.authorAswathi, K K
dc.contributor.authorKAU
dc.date.accessioned2019-11-25T10:09:43Z
dc.date.available2019-11-25T10:09:43Z
dc.date.issued2014
dc.descriptionPGen_US
dc.description.abstractWatermelon, Citrullus lanatus (Thunb.), is an annual trailing creeper belonging to the family Cucurbitaceae. It occupies a pivotal position among fruit vegetables. Among the diseases affecting watermelon, those caused by viruses are difficult to control and can be very destructive. Recently, bud necrosis, a Tospovirus disease, has emerged as a serious problem of watermelon cultivation in Kerala. Not much work on the various aspects of the disease has been carried out. Further, little is known on disease incidence, severity and mode of transmission of the disease which are crucial for evolving appropriate management practices. Hence, the present project was undertaken to study the symptomatology, transmission, physical properties, host range and serological reaction of Watermelon bud necrosis virus (WBNV). Survey undertaken on the incidence and severity of the disease in major watermelon growing locations of Thrissur, Palakkad, Malappuram, Kasaragod and Kollam districts revealed the variations, based on the genotype, season and location. Under natural conditions, symptoms observed were curling, mottling, narrowing of leaf lamina, stunting, necrotic streaks on stem, unopening of flower buds and their necrosis, necrotic rings and malformation of fruits. Under artificial inoculation, symptom initiated as curling, crinkling and mottling of leaves, which later spread to young leaves and resulted in brittleness. The virus was isolated from symptomatic watermelon plants by mechanical transmission through a local lesion host Amaranthus viridis using potassium phosphate buffer pH 7.0. Transmission studies proved that WBNV transmitted both by sap and vector. Citrate phosphate buffer 0.1M (pH 7.2) showed the maximum transmission (72.22 %) with the minimum incubation period (8 days) and was used for further studies. The insect vector of WBNV was identified as Thrips palmi Karny. Studies on virus vector relationships showed that the minimum acquisition access period and inoculation access period were 24 h and 48 h respectively. Physical properties of virus i.e., dilution end point, thermal inactivation point and longevity in in vitro were investigated and it was found that the virus was inactivated at dilutions between 10-2 and 10-3 and at temperatures between 45 and 500C. Longevity in in vitro was recorded as four h at room temperature (28± 2) and 24 h under refrigerated condition (80 C). Host range studies revealed that ridge gourd, bottle gourd, salad cucumber, bitter gourd, cowpea, groundnut and gomphrena could serve as collateral hosts of the virus. Serological tests using DAC – ELISA of WBNV revealed close relation of the virus with Peanut bud necrosis virus. Among the 22 genotypes of watermelon screened for response to the virus none of them showed resistance. However, WMH531 and WMH 12031 recorded the lowest incidence of 10 and 8.33 per cent respectively, while the highest (96 per cent) was in NS 295 hybrid.en_US
dc.identifier.urihttp://krishikosh.egranth.ac.in/handle/1/5810136129
dc.keywordsTospoviruses, Transmission, Immunodetection and diagnosisen_US
dc.language.isoenen_US
dc.publisherDepartment of Plant Pathology, College of Horticulture, Vellanikkaraen_US
dc.subPlant Pathologyen_US
dc.subjectnullen_US
dc.themeBiological characterization of bud necrosis virus diseaseen_US
dc.these.typeM.Scen_US
dc.titleBiological characterization of bud necrosis virus disease in watermelon(Citrullus lanatus T.)en_US
dc.typeThesisen_US
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