韩国苹果感染病毒的深度测序分析

I. Cho, D. Igori, Seungmo Lim, G. Choi, J. Hammond, Hyoun-Sub Lim, J. Moon
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引用次数: 13

摘要

深度测序已经产生了来自5种病毒的52个contigs;从8个小叶和/或生长迟缓的苹果样品中鉴定出苹果萎绿叶斑病病毒(ACLSV)、苹果茎沟病毒(ASGV)、苹果茎点蚀病毒(ASPV)、苹果绿皱伴随病毒(AGCaV)和杏潜伏病毒(ApLV)。与5个病毒基因组的参考序列相比,组装的contigs核苷酸(nt)序列的一致性为68% ~ 99%。其中,asv和ASGV序列以52个contigs最为丰富。采用RT-PCR方法,根据各序列的特异性引物,确定了5种病毒的存在。在三个样本中检测到所有五种病毒,而所有样本都混合感染了至少两种病毒。检测到最多的病毒是ASPV,其次是ASGV、ApLV、ACLSV和AGCaV,这些病毒在混合感染中也有发现。AGCaV在编号为1012480和93549的组装序列中被鉴定出来,与AGCaV分离株Aurora-1的ORF1序列同源性分别为82%和78%。ApLV在ID 65587、1802365和116777三个组装片段中被鉴定出来,分别与ApLV分离物LA2的ORF1序列同源性分别为77%、78%和76%。深度测序技术被证明是检测和鉴定受感染苹果树中已知和未知病毒的一种有价值和强大的工具,本研究首次鉴定了韩国商业果园中的ApLV和AGCaV。
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Deep Sequencing Analysis of Apple Infecting Viruses in Korea
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.
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