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Deep Sequencing Analysis of Apple Infecting Viruses in Korea

机译:韩国苹果感染病毒的深度测序分析

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摘要

Deep sequencing has generated 52 contigs derived from five viruses; Apple chlorotic leaf spot virus (ACLSV), Apple stem grooving virus (ASGV), Apple stem pitting virus (ASPV), Apple green crinkle associated virus (AGCaV), and Apricot latent virus (ApLV) were identified from eight apple samples showing small leaves and/or growth retardation. Nucleotide (nt) sequence identity of the assembled contigs was from 68% to 99% compared to the reference sequences of the five respective viral genomes. Sequences of ASPV and ASGV were the most abundantly represented by the 52 contigs assembled. The presence of the five viruses in the samples was confirmed by RT-PCR using specific primers based on the sequences of each assembled contig. All five viruses were detected in three of the samples, whereas all samples had mixed infections with at least two viruses. The most frequently detected virus was ASPV, followed by ASGV, ApLV, ACLSV, and AGCaV which were withal found in mixed infections in the tested samples. AGCaV was identified in assembled contigs ID 1012480 and 93549, which showed 82% and 78% nt sequence identity with ORF1 of AGCaV isolate Aurora-1. ApLV was identified in three assembled contigs, ID 65587, 1802365, and 116777, which showed 77%, 78%, and 76% nt sequence identity respectively with ORF1 of ApLV isolate LA2. Deep sequencing assay was shown to be a valuable and powerful tool for detection and identification of known and unknown virome in infected apple trees, here identifying ApLV and AGCaV in commercial orchards in Korea for the first time.
机译:深度测序产生了来自五种病毒的52个重叠群。从八个显示小叶子的苹果样品中鉴定出苹果绿化叶斑病毒(ACLSV),苹果茎沟病毒(ASGV),苹果茎凹陷病毒(ASPV),苹果绿皱纹相关病毒(AGCaV)和杏潜伏病毒(ApLV)。和/或发育迟缓。与五个相应病毒基因组的参考序列相比,组装的重叠群的核苷酸(nt)序列同一性为68%至99%。 ASPV和ASGV的序列由52个重叠群组成。基于每个组装的重叠群的序列,使用特定引物通过RT-PCR确认了样品中五种病毒的存在。在三个样本中检测到所有五种病毒,而所有样本中至少有两种病毒混合感染。被检测到最频繁的病毒是ASPV,其次是ASGV,ApLV,ACLSV和AGCaV,它们在被测样品的混合感染中均被发现。在组装的重叠群ID 1012480和93549中鉴定出AGCaV,其与AGCaV分离株Aurora-1的ORF1显示82%和78%的nt序列同一性。在三个组装的重叠群中鉴定出ApLV,ID 65587、1802365和116777,它们分别显示与ApLV分离株LA2的ORF1的77%,78%和76%nt序列同一性。事实证明,深度测序测定法是检测和鉴定感染苹果树中已知和未知病毒的有价值且功能强大的工具,这是首次在韩国商业果园中鉴定ApLV和AGCaV。

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