Droplet-vitrification cryotherapy and thermotherapy as efficient tools for the eradication of apple chlorotic leaf spot virus and apple stem grooving virus from virus-infected quince in vitro cultures

被引:16
作者
Farhadi-Tooli, Sakineh [1 ]
Ghanbari, Alireza [1 ]
Kermani, Maryam Jafarkhani [2 ]
Zeinalabedini, Mehrshad [3 ]
Bettoni, Jean Carlos [4 ]
Naji, Amir Mohammad [5 ]
Kazemi, Nooshin [6 ]
机构
[1] Univ Mohaghegh Ardabili, Fac Agr & Nat Resources, Dept Hort Sci, POB 179, Ardebil, Iran
[2] Agr Res Educ & Extens Org AREEO, Agr Biotechnol Res Inst Iran ABRII, Dept Tissue & Cell Culture, Karaj 3135933151, Iran
[3] Agr Res Educ & Extens Org AREEO, Agr Biotechnol Res Inst Iran ABRII, Dept Syst & Synthet Biol, Karaj 3135933151, Iran
[4] New Zealand Inst Plant & Food Res Ltd, Private Bag 11600, Palmerston North 4442, New Zealand
[5] Shahed Univ, Dept Agron & Plant Breeding, Fac Agr, Tehran, Iran
[6] Agr Res Educ & Extens Org AREEO, Temperate Fruits Res Ctr, Hort Sci Res Inst, Karaj, Iran
关键词
Cydonia oblonga mill; ACLSV; ASGV; Virus-free material; Virus disease; Cryopreservation; CUCUMBER-MOSAIC-VIRUS; SHOOT-TIP CULTURE; PITTING-VIRUS; ENCAPSULATION-DEHYDRATION; CYDONIA-OBLONGA; LATENT VIRUSES; ELIMINATION; CRYOPRESERVATION; VITIS; RNA;
D O I
10.1007/s10658-021-02400-x
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
Viral diseases affect quince plant productivity and fruit quality. This study evaluated the effectiveness of droplet-vitrification cryotherapy and thermotherapy methods in the eradication of apple chlorotic leaf spot virus (ACLSV) and apple stem grooving virus (ASGV) from virus-infected in vitro cultures of quince rootstock 'QA' and cultivar 'Neyshabour'. In vitro cultures infected with ACLSV and ASGV were thermo-treated at 38 degrees C for 0, 7, 10, and 15 days followed by apical shoot tip isolation. In the cryotherapy procedure, shoot tips were incubated on preculture medium and then exposed to plant vitrification solution 2 for 30 min at 0 degrees C prior to liquid nitrogen (LN) exposure. Shoot tips were warmed in unloading solution and placed on recovered medium. The frequency of virus eradication was determined using RT-PCR in plantlets recovered from thermo-and cryo-treatments and controls that were grown under in vitro conditions for 4 months. Droplet-vitrification cryotherapy and thermotherapy resulted in high frequencies of ACLSV and ASGV eradication from in vitro cultures of quince. The results showed that increasing the duration of thermotherapy significantly increased virus eradication. In vitro shoots of quince rootstock 'QA' and cultivar 'Neyshabour' heat-treated for 10 days were 64% and 67% free of ACLSV and 55% and 33% free of ASGV, respectively. All quince rootstock 'QA' plantlets regenerated from droplet-vitrification cryotherapy and RT-PCR assessed were free of ACLSV and 67% were free of ASGV. Cryotherapy and thermotherapy may be considered as promising methods for virus eradication programs in quince genotypes facilitating the production of healthy stock plants.
引用
收藏
页码:31 / 43
页数:13
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