首页> 外文期刊>Annals of Applied Biology >Shoot tip culture and cryopreservation for eradication of Apple stem pitting virus (ASPV) and Apple stem grooving virus (ASGV) from apple rootstocks 'M9' and 'M26'
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Shoot tip culture and cryopreservation for eradication of Apple stem pitting virus (ASPV) and Apple stem grooving virus (ASGV) from apple rootstocks 'M9' and 'M26'

机译:进行芽尖培养和冷冻保存,以根除苹果砧木“ M9”和“ M26”中的苹果茎凹陷病毒(ASPV)和苹果茎切槽病毒(ASGV)

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This study attempted to eradicate Apple stem pitting virus (ASPV) and Apple stem grooving virus (ASGV) from virus-infected in vitro shoots of apple rootstocks 'M9' and 'M26' using shoot tip culture and cryopreservation. In shoot tip culture, shoot tips (0.2 mm in length) containing two leaf primordia failed to show shoot regrowth. Although shoot regrowth rate was the highest in the largest shoot tips (1.0 mm in length) containing four leaf primordia, none of the regenerated shoots was virus-free. Shoot tips (0.5 mm in length) containing two and three leaf primordia produced 100% and 10% of ASPV-free shoots, respectively, while those (1.0 mm) containing four leaf primordia were not able to eradicate ASPV. ASGV could not be eradicated by shoot tip culture, regardless of the size of the shoot tips tested. In cryopreservation, shoot tips (0.5 mm in length) containing two leaf primordia did not resume shoot growth. Although 1.0-mm and 1.5-mm shoot tips gave similarly high ASPV-free frequencies, the latter had much higher shoot regrowth rate than the former. Very similar results of shoot regrowth and virus eradication by shoot tip culture and cryopreservation were observed in both 'M9' and 'M26'. Histological observations showed that only cells in upper part of apical dome and in leaf primordia 1-3 survived, while other cells were damaged or killed, in shoot tips following cryopreservation. Virus immunolocalization found ASPV was not detected in upper part of apical dome and leaf primordia 1 and 2, but was present in lower part of apical dome, and in leaf primordium 4 and more developed tissues in all samples tested. ASPV was also detected in leaf primordium 3 in about 16.7% and 13.3% samples tested in 'M9' and 'M26'. ASGV was observed in apical dome and leaf primordia 1-6, leaving only a few top layers of cells in apical dome free of the virus. Different abilities of ASPV and ASGV to invade leaf petioles and shoot tips were also noted.
机译:这项研究试图使用茎尖培养和冷冻保存技术,从感染了苹果砧木“ M9”和“ M26”的离体芽中根除苹果茎凹陷病毒(ASPV)和苹果茎切槽病毒(ASGV)。在茎尖培养中,含有两个叶片原基的茎尖(长度为0.2 mm)未能显示茎长大。尽管在包含四个叶片原基的最大枝条尖端(长度为1.0 mm)中枝条的再生速率最高,但再生的枝条均不含病毒。包含两个和三个叶片原基的茎尖(长度为0.5 mm)分别产生100%和10%的无ASPV芽,而含有四个叶片原基的茎尖(1.0 mm)不能根除ASPV。无论所测芽尖的大小如何,都无法通过芽尖培养根除ASGV。在冷冻保存中,含有两个叶片原基的芽尖(长度为0.5 mm)不能恢复芽的生长。尽管1.0毫米和1.5毫米的芽尖给出了类似的高无ASPV频率,但后者的芽再生长率比前者高得多。在“ M9”和“ M26”中均观察到非常相似的结果,即通过芽尖培养和冷冻保存消除了芽的再生和病毒。组织学观察表明,在冷冻保存后的芽梢中,仅顶端圆顶上部和叶原基1-3中的细胞存活,而其他细胞被破坏或杀死。病毒免疫定位发现,在所有测试样品中,未在顶端圆顶和叶原基1和2的上部检测到ASPV,但在顶端圆顶的下部,叶原基4和更发达的组织中检测到ASPV。在“ M9”和“ M26”中测试的约16.7%和13.3%的样品中,在原叶3中也检测到ASPV。在根尖穹顶和叶片原基1-6中观察到ASGV,在根尖穹顶中仅保留了几层顶层细胞不含病毒。还指出了ASPV和ASGV侵害叶柄和芽梢的不同能力。

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