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中国番木瓜杆状DNA病毒2全基因组序列分析的首次报道。

First report of the whole‑genome sequence analysis of Fig badnavirus 2 from China.

作者信息

Aizitili Tuxunaili, Maimaiti Yushanjiang, Zhang Zhixiang, Mijiti Maihemuti

机构信息

College of Agronomy, Key Laboratory of Prevention and Control of Invasive Alien Species in Agriculture & Forestry of the North-Western Desert Oasis, Ministry of Agriculture and Rural Affairs, Xinjiang Agricultural University, Urumqi, 830052, China.

MOE Key Laboratory of Bioinformatics, Center for Plant Biology, Tsinghua-Peking Joint Center for Life Sciences, School of Life Sciences, Tsinghua University, Beijing, 100084, China.

出版信息

Virus Genes. 2025 Apr;61(2):214-219. doi: 10.1007/s11262-024-02132-0. Epub 2025 Jan 8.

Abstract

A novel plant virus was identified in fig trees exhibiting ring spot symptoms through high-throughput sequencing (HTS). The complete genome sequence was successfully determined using PCR and RT-PCR techniques. The virus features a circular DNA genome of 7233 nucleotides (nt) in length, encompassing four open reading frames (ORFs). ORF1 and ORF2 encode hypothetical proteins, while ORF3 encodes a putative polyprotein with conserved domains, including a zinc finger, aspartic protease, reverse transcriptase (RT), and RNase H. ORF4 encodes a putative protein of unknown function. Comparative nucleotide sequence analysis of the RT + RNase H region reveals 84.46% and 78.82% identity with grapevine badnavirus 1 (GBV-1, MF781082.1) and fig badnavirus 1 (FBV-1, MK348055.1), respectively. Notably, this virus's genomic organization diverges from GBV-1 but is similar to FBV-1. Phylogenetic analysis demonstrates that the three isolates of this virus form a distinct clade within the badnaviruses. Based on genomic structure and phylogenetic relationships, this novel virus represents a new member of the genus Badnavirus and is proposed to be named "Fig badnavirus 2" (FBV-2).

摘要

通过高通量测序(HTS)在表现出环斑症状的无花果树上鉴定出一种新型植物病毒。利用聚合酶链反应(PCR)和逆转录聚合酶链反应(RT-PCR)技术成功测定了其完整基因组序列。该病毒具有一个长度为7233个核苷酸(nt)的环状DNA基因组,包含四个开放阅读框(ORF)。ORF1和ORF2编码假定蛋白,而ORF3编码一个具有保守结构域的假定多蛋白,包括一个锌指、天冬氨酸蛋白酶、逆转录酶(RT)和核糖核酸酶H。ORF4编码一个功能未知的假定蛋白。对RT + 核糖核酸酶H区域的比较核苷酸序列分析显示,与葡萄藤杆状DNA病毒1(GBV-1,MF781082.1)和无花果杆状DNA病毒1(FBV-1,MK348055.1)的同一性分别为84.46%和78.82%。值得注意的是,该病毒的基因组结构与GBV-1不同,但与FBV-1相似。系统发育分析表明,该病毒的三个分离株在杆状DNA病毒中形成一个独特的进化枝。基于基因组结构和系统发育关系,这种新型病毒代表杆状DNA病毒属的一个新成员,并被提议命名为“无花果杆状DNA病毒2”(FBV-2)。

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