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重组草莓脉带病毒DNA的感染性。

Infectivity of recombinant strawberry vein banding virus DNA.

作者信息

Mahmoudpour Ali

机构信息

Department of Plant Pathology, University of California Davis, Davis, CA 95616, USA.

出版信息

J Gen Virol. 2003 Jun;84(Pt 6):1377-1381. doi: 10.1099/vir.0.18994-0.

Abstract

Infectivity of the cloned DNA genome of strawberry vein banding virus (SVBV) was demonstrated by particle bombardment of 4-week-old strawberry (Fragaria vesca L. var. UC-5) plants with gold particles coated with the putative full-length 7.9 kb viral DNA. Vein banding symptoms developed on 15 % of inoculated plants 6-7 weeks post-inoculation. An approximate 1.25-mer of the viral DNA was cloned into the binary vector pCGN1547. Particle bombardment of this construct into strawberry plants gave an infection rate of 75 %. The construct was used for transformation of Agrobacterium tumefaciens, and infiltration of these cells into healthy strawberry leaves resulted in development of vein banding symptoms in 100 % of inoculated plants. Gel electrophoresis, Southern blot hybridization with an SVBV probe and sequence analyses of PCR-amplified DNA fragments were used to confirm SVBV infection in symptomatic plants.

摘要

通过用包被有假定全长7.9 kb病毒DNA的金颗粒对4周龄草莓(弗吉尼亚草莓UC-5变种)植株进行粒子轰击,证明了草莓脉带病毒(SVBV)克隆DNA基因组的感染性。接种后6 - 7周,15%的接种植株出现脉带症状。将大约1.25倍体的病毒DNA克隆到二元载体pCGN1547中。将该构建体对草莓植株进行粒子轰击,感染率为75%。该构建体用于根癌农杆菌的转化,将这些细胞渗入健康草莓叶片后,100%的接种植株出现脉带症状。利用凝胶电泳、用SVBV探针进行Southern杂交以及对PCR扩增的DNA片段进行序列分析,以确认有症状植株中SVBV的感染情况。

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