Elimination of Eight Viruses and Two Viroids from Preclonal Candidates of Six Grapevine Varieties (<i>Vitis vinifera</i> L.) through In Vivo Thermotherapy and In Vitro Meristem Tip Micrografting

Viruses and virus-like organisms are a major problem in viticulture worldwide. 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...

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Main Authors: Vanja Miljanić, Denis Rusjan, Andreja Škvarč, Philippe Chatelet, Nataša Štajner
Format: Article
Language:English
Published: MDPI AG 2022-04-01
Series:Plants
Subjects:
Online Access:https://www.mdpi.com/2223-7747/11/8/1064
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author Vanja Miljanić
Denis Rusjan
Andreja Škvarč
Philippe Chatelet
Nataša Štajner
author_facet Vanja Miljanić
Denis Rusjan
Andreja Škvarč
Philippe Chatelet
Nataša Štajner
author_sort Vanja Miljanić
collection DOAJ
description Viruses and virus-like organisms are a major problem in viticulture worldwide. 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 (<i>Vitis labrusca</i> × <i>Vitis riparia</i>), 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 (<i>Vitis vinifera</i> 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.
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spelling doaj.art-6eaae6032aa34a9aa038ea9ec39ea4392023-11-30T21:46:34ZengMDPI AGPlants2223-77472022-04-01118106410.3390/plants11081064Elimination of Eight Viruses and Two Viroids from Preclonal Candidates of Six Grapevine Varieties (<i>Vitis vinifera</i> L.) through In Vivo Thermotherapy and In Vitro Meristem Tip MicrograftingVanja Miljanić0Denis Rusjan1Andreja Škvarč2Philippe Chatelet3Nataša Štajner4Department of Agronomy, Biotechnical Faculty, University of Ljubljana, 1000 Ljubljana, SloveniaDepartment of Agronomy, Biotechnical Faculty, University of Ljubljana, 1000 Ljubljana, SloveniaChamber of Agriculture and Forestry of Slovenia, Agriculture and Forestry Institute Nova Gorica, 5000 Nova Gorica, SloveniaUMR AGAP Institut, Univ. Montpellier, CIRAD, INRAE, Institut Agro, F-34398 Montpellier, FranceDepartment of Agronomy, Biotechnical Faculty, University of Ljubljana, 1000 Ljubljana, SloveniaViruses and virus-like organisms are a major problem in viticulture worldwide. 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 (<i>Vitis labrusca</i> × <i>Vitis riparia</i>), 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 (<i>Vitis vinifera</i> 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.https://www.mdpi.com/2223-7747/11/8/1064<i>Vitis vinifera</i> L.grapevine viruses and viroidsthermotherapymicrografting
spellingShingle Vanja Miljanić
Denis Rusjan
Andreja Škvarč
Philippe Chatelet
Nataša Štajner
Elimination of Eight Viruses and Two Viroids from Preclonal Candidates of Six Grapevine Varieties (<i>Vitis vinifera</i> L.) through In Vivo Thermotherapy and In Vitro Meristem Tip Micrografting
Plants
<i>Vitis vinifera</i> L.
grapevine viruses and viroids
thermotherapy
micrografting
title Elimination of Eight Viruses and Two Viroids from Preclonal Candidates of Six Grapevine Varieties (<i>Vitis vinifera</i> L.) through In Vivo Thermotherapy and In Vitro Meristem Tip Micrografting
title_full Elimination of Eight Viruses and Two Viroids from Preclonal Candidates of Six Grapevine Varieties (<i>Vitis vinifera</i> L.) through In Vivo Thermotherapy and In Vitro Meristem Tip Micrografting
title_fullStr Elimination of Eight Viruses and Two Viroids from Preclonal Candidates of Six Grapevine Varieties (<i>Vitis vinifera</i> L.) through In Vivo Thermotherapy and In Vitro Meristem Tip Micrografting
title_full_unstemmed Elimination of Eight Viruses and Two Viroids from Preclonal Candidates of Six Grapevine Varieties (<i>Vitis vinifera</i> L.) through In Vivo Thermotherapy and In Vitro Meristem Tip Micrografting
title_short Elimination of Eight Viruses and Two Viroids from Preclonal Candidates of Six Grapevine Varieties (<i>Vitis vinifera</i> L.) through In Vivo Thermotherapy and In Vitro Meristem Tip Micrografting
title_sort elimination of eight viruses and two viroids from preclonal candidates of six grapevine varieties i vitis vinifera i l through in vivo thermotherapy and in vitro meristem tip micrografting
topic <i>Vitis vinifera</i> L.
grapevine viruses and viroids
thermotherapy
micrografting
url https://www.mdpi.com/2223-7747/11/8/1064
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