摘要
以草莓品种明宝为材料,取茎尖做初代培养,继代扩繁5次后,取2mm左右的茎尖,利用玻璃化超低温技术对SMYEV进行脱除,并利用结合内标的多重RT-PCR技术对再生植株进行病毒检测。结果表明,在病毒脱除过程中,预培养蔗糖浓度为0.5mol/L,处理3d;装载处理为25℃,60min;玻璃化处理为0℃,120min;液氮处理60min后,进行40℃水浴2min,草莓茎尖的存活率为76%,而草莓轻型黄边病毒的脱除率为95%。只有通过液氮处理才可以脱除该病毒,液氮处理前的玻璃化处理脱毒率为0。利用超低温脱毒法可以简便有效地脱除SMYEV。
The surface-sterilized shoot tips of Fragaria ananassa cv. Meihou infected with strawberry mild yellow edge virus (SMYEV)were cultured five times in vitro and the shoot tips (about 2 mm in size) were cryopreserved. The SMYEV of regenerated plants were detected by multiplex RT-PCR combined with internal control. The shoot tips were pre-cuhured on basic medium with sucrose concentration of 0.5 mol/L for 3 days,then the pre-euhured shoot tips were loaded for 60 min at 25℃, vitrified with PVS2 for 120 rain at 0 ℃ immersed directly in liquid nitrogen for 60 rain and rewarmed in 40℃ for 2 rain. The result showed that the percent of survival shoot tips was 76%, but the various steps taken before freezing in liquid nitrogen did not eliminate SMYEV. However, the freezing step could successfully eliminate SMYEV and the percentage of virus-free shoot tips reached 95%.
出处
《果树学报》
CAS
CSCD
北大核心
2008年第6期872-876,共5页
Journal of Fruit Science
基金
江苏省科技厅科技攻关项目(Be2007351)
江苏省农业资源开发局项目(2008KJ-D47)
南京农业大学SRT资助项目(0803A22)
关键词
草莓
草莓轻型黄边病毒
超低温
玻璃化
脱毒
Strawberry
Strawberry mild yellow edge virus
Cryopreservation
Vitrification
Virus elimination