Please use this identifier to cite or link to this item: http://earsiv.odu.edu.tr:8080/xmlui/handle/11489/1464
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dc.contributor.authorDeligoz, Ilyas-
dc.contributor.authorErper, Ismail-
dc.contributor.authorOzer, Goksel-
dc.contributor.authorTurkkan, Muharrem-
dc.contributor.authorYildirim, Elif-
dc.date.accessioned2022-08-15T12:38:13Z-
dc.date.available2022-08-15T12:38:13Z-
dc.date.issued2019-
dc.identifier.urihttp://doi.org/10.1007/s42161-018-00201-6-
dc.identifier.urihttp://earsiv.odu.edu.tr:8080/xmlui/handle/11489/1464-
dc.description.abstractTulip (Tulipa L.) is one of the most important flower bulb crops with production of approximately forty-five million units as cut flowers in Turkey (Anonymous 2018). In 2018, some lants showed disease symptoms consisting of water-soaked spots on petals and leaves in tulip nurseries in Samsun province. Infected plant tissues were cut into small pieces, placed on Tulip Leaf Agar medium after surface sterilization, and incubated at 18 °C for five days. The conidia were unicellular, ellipsoid to ovoid, pale-brown, and measured 8.16–10.58 × 12.18–18.48 μm (average 8.8 × 14.86 μm). The conidiophores were erect, cylindrical, deep brown in color except hyaline swollen bases, and measured 650–830 μm high. The sclerotia were black, small, circular, 0.96–1.22 mm in diameter and arranged uniformly on the medium. These morphological characteristics identified the fungus as Botrytis tulipae according to Ellis (1971). To confirm identification, the internal transcribed spacer (ITS) region of rDNA (amplified with ITS1/ITS4 primers), two nuclear genes encoding glyceraldehyde-3-phosphate dehydrogenase (G3PDH) and RNA polymerase subunit II (RPB2) (amplified with G3PDHf/ G3PDHr and RPB2f/RPB2r primers) of a representative isolate (Tr-Bt03) were sequenced (White et al. 1990; Staats et al. 2005). The ITS, G3PDH and RPB2 sequences of Tr-Bt03 isolate (MH382821, MH392210 and MH392209, respectively) were 100% identical to those of B. tulipae isolates (Bt9601, Bt9806, Bt9815 and Bt9903) in Genbank. For assessing pathogenicity, the wax layer of leaves of five healthy tulip plants was slightly damaged by hand rubbing, and then five-month-old plants were sprayed with the suspension of conidia (1 × 105 conidia mL−1 ). Uninfected leaves of the plant with similar features were used as control. Five days after inoculation, typical symptoms appeared on leaves and flowers of all inoculated plants, but not on control plants. To our knowledge, this is the first report of Botrytis blight of tulip caused by B. tulipae in Turkeyen_US
dc.language.isoengen_US
dc.publisherSPRINGER, 233 SPRING ST, NEW YORK, NY 10013 USAen_US
dc.relation.isversionof10.1007/s42161-018-00201-6en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectTulip; Botrytis tulipae; rDNA-ITS regionen_US
dc.titleFirst report of botrytis blight of tulip caused by Botrytis tulipae in Turkeyen_US
dc.typearticleen_US
dc.relation.journalJOURNAL OF PLANT PATHOLOGYen_US
dc.contributor.departmentOrdu Üniversitesien_US
dc.contributor.authorID0000-0001-7779-9365en_US
dc.identifier.volume101en_US
dc.identifier.issue2en_US
dc.identifier.startpage427en_US
dc.identifier.endpage427en_US
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