Yang Zefen, Chen Zeli, Bakht Faryal, Li Shangyun, Zi Shaomei, Li Xin, Zhao Xiyan, Wen Guosong, Zhao Mingfu
Key Laboratory for Agricultural Biodiversity for Pest Management of China, Ministry of Education, Yunnan Agricultural University, No. 95, Jinhei Road, Panlong District, Kunming, 650201, Yunnan, China.
College of Agronomy and Biotechnology, Yunnan Agricultural University, No. 95, Jinhei Road, Panlong District, Kunming, 650201, Yunnan, China.
Arch Virol. 2024 Apr 15;169(5):97. doi: 10.1007/s00705-024-06023-5.
The complete genome sequence of a novel badnavirus, tentatively named "fatsia badnavirus 1" (FaBV1, OM540428), was identified in Fatsia japonica. The infected plant displayed virus-like symptoms on leaves, including yellowing and chlorosis. The genome of FaBV1 is 7313 bp in length and similar in size and organization to other members of the genus Badnavirus (family Caulimoviridae), containing four open reading frames (ORFs), three of which are found in all known badnaviruses, and the other of which is only present in some badnaviruses. The virus has the genome characteristics of badnaviruses, including a tRNA binding site (5'-TCTGAATTTATAGCGCTA-3') and two cysteine-rich domains (C-X-C-2X-C-4X-H-4X-C and C-2X-C-11X-C-2X-C-4X-C-2X-C). Pairwise sequence comparisons of the RT+RNase H region indicated that FaBV1 shares 61.4-71.2% nucleotide (nt) sequence identity with other known badnaviruses, which is below the threshold (80% nt sequence identity in the RT+RNase H region) used for species demarcation in the genus Badnavirus. Phylogenetic analysis revealed that FaBV1, ivy ringspot-associated virus (IRSaV, MN850490.1), and cacao mild mosaic virus (CMMV, KX276640.1) together form a separate clade within the genus Badnavirus, suggesting that FaBV1 is a new member of the genus Badnavirus in the family Caulimoviridae. To our knowledge, this is the first report of a badnavirus infecting F. japonica.
在日本八角金盘(Fatsia japonica)中鉴定出一种新型杆状DNA病毒的完整基因组序列,暂命名为“八角金盘杆状DNA病毒1”(FaBV1,OM540428)。受感染的植株叶片上出现了类似病毒的症状,包括黄化和褪绿。FaBV1的基因组长度为7313 bp,大小和结构与杆状DNA病毒属(花椰菜花叶病毒科)的其他成员相似,包含四个开放阅读框(ORF),其中三个在所有已知杆状DNA病毒中都存在,另一个仅存在于一些杆状DNA病毒中。该病毒具有杆状DNA病毒的基因组特征,包括一个tRNA结合位点(5'-TCTGAATTTATAGCGCTA-3')和两个富含半胱氨酸的结构域(C-X-C-2X-C-4X-H-4X-C和C-2X-C-11X-C-2X-C-4X-C-2X-C)。逆转录酶+核糖核酸酶H区域的成对序列比较表明,FaBV1与其他已知杆状DNA病毒的核苷酸(nt)序列同一性为61.4-71.2%,低于杆状DNA病毒属物种划分所用的阈值(逆转录酶+核糖核酸酶H区域中nt序列同一性为80%)。系统发育分析表明,FaBV1、常春藤环斑相关病毒(IRSaV,MN850490.1)和可可轻度花叶病毒(CMMV,KX276640.1)在杆状DNA病毒属内共同形成一个单独的分支,这表明FaBV1是花椰菜花叶病毒科杆状DNA病毒属的一个新成员。据我们所知,这是关于杆状DNA病毒感染日本八角金盘的首次报道。