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<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dc="http://purl.org/dc/elements/1.1/"><rdf:Description rdf:about="https://repozitorij.uni-lj.si/IzpisGradiva.php?id=136431"><dc:title>Elimination of eight viruses and two viroids from preclonal candidates of six grapevine varieties (Vitis vinifera L.) through in vivo thermotherapy and in vitro meristem tip micrografting</dc:title><dc:creator>Miljanić,	Vanja	(Avtor)
	</dc:creator><dc:creator>Rusjan,	Denis	(Avtor)
	</dc:creator><dc:creator>Škvarč,	Andreja	(Avtor)
	</dc:creator><dc:creator>Chatelet,	Philippe	(Avtor)
	</dc:creator><dc:creator>Štajner,	Nataša	(Avtor)
	</dc:creator><dc:subject>Vitis vinifera L.</dc:subject><dc:subject>grapevine</dc:subject><dc:subject>viruses</dc:subject><dc:subject>viroids</dc:subject><dc:subject>micrografting</dc:subject><dc:subject>thermotherapy</dc:subject><dc:description>Viruses and virus-like organisms are amajor problemin viticultureworldwide. They cannot be controlled by standard plant protection measures, and once infected, plants remain infected throughout their life; therefore, the propagation of healthy vegetative material is crucial. In vivo thermotherapy at 36–38 °C for at least six weeks, followed by meristem tip micrografting (0.1–0.2 mm) onto in vitro-growing seedling rootstocks of Vialla (Vitis labrusca × Vitis riparia), was successfully used to eliminate eight viruses (grapevine rupestris stem pitting-associated virus (GRSPaV), grapevine Pinot gris virus (GPGV), grapevine fanleaf virus (GFLV), grapevine leafroll-associated virus 3 (GLRaV-3), grapevine fleck virus (GFkV), grapevine rupestris vein feathering virus (GRVFV), grapevine Syrah virus-1 (GSyV-1), and raspberry bushy dwarf virus (RBDV)), as well as two viroids (hop stunt viroid (HSVd) and grapevine yellow speckle viroid 1 (GYSVd-1)) from preclonal candidates of six grapevine varieties (Vitis vinifera L.). A half-strength MS medium including vitamins supplemented with 30 g/L of sucrose and solidified with 8 g/L of agar, without plant growth regulators, was used for the growth and root development of micrografts and the subsequently micropropagated plants; no callus formation, hyperhydricity, or necrosis of shoot tips was observed. Although the overall regeneration was low (higher in white than in red varieties), a 100% elimination was achieved for all eight viruses, whereas the elimination level for viroids was lower, reaching only 39.2% of HSVd-free and 42.6% GYSVd-1-free vines. To the best of our knowledge, this is the first report of GPGV, GRVFV, GSyV-1, HSVd, and GYSVd-1 elimination through combining in vivo thermotherapy and in vitro meristem tip micrografting, and the first report of RBDV elimination from grapevines. The virus-free vines were successfully acclimatized in rockwool plugs and then transferred to soil.</dc:description><dc:date>2022</dc:date><dc:date>2022-05-04 08:43:48</dc:date><dc:type>Članek v reviji</dc:type><dc:identifier>136431</dc:identifier><dc:language>sl</dc:language></rdf:Description></rdf:RDF>
