Wu Chien-Fu, Aoki Nanako, Takeshita Naoki, Fukuhara Toshiyuki, Chiura Hiroshi X, Arie Tsutomu, Kotta-Loizou Ioly, Okada Ryo, Komatsu Ken, Moriyama Hiromitsu
Laboratory of Molecular and Cellular Biology, Tokyo University of Agriculture and Technology, Fuchu, Japan.
Laboratory of Plant Pathology, Tokyo University of Agriculture and Technology, Fuchu, Japan.
Front Microbiol. 2021 Oct 22;12:773062. doi: 10.3389/fmicb.2021.773062. eCollection 2021.
Alternaria alternata virus 1 (AaV1) has been identified in the saprophytic fungus strain EGS 35-193. AaV1 has four genomic double-stranded (ds)RNA segments (dsRNA1-4) packaged in isometric particles. The 3' end of each coding strand is polyadenylated (36-50nt), but the presence of a cap structure at each 5' end has not previously been investigated. Here, we have characterized the AaV1 genome and found that it has unique features among the mycoviruses. We confirmed the existence of cap structures on the 5' ends of the AaV1 genomic dsRNAs using RNA dot blots with anti-cap antibodies and the oligo-capping method. Polyclonal antibodies against purified AaV1 particles specifically bound to an 82kDa protein, suggesting that this protein is the major capsid component. Subsequent Edman degradation indicated that the AaV1 dsRNA3 segment encodes the major coat protein. Two kinds of defective AaV1 dsRNA2, which is 2,794bp (844 aa) in length when intact, appeared in EGS 35-193 during subculturing, as confirmed by RT-PCR and northern hybridization. Sequence analysis revealed that one of the two defective dsRNA2s contained a 231bp deletion, while the other carried both the 231bp deletion and an additional 465bp deletion in the open reading frame. Both deletions occurred in-frame, resulting in predicted proteins of 767 aa and 612 aa. The fungal isolates carrying virions with the defective dsRNA2s showed impaired growth and abnormal pigmentation. To our best knowledge, AaV1 is the first dsRNA virus to be identified with both 5' cap and 3'poly(A) structures on its genomic segments, as well as the specific deletions of dsRNA2.
链格孢病毒1(AaV1)已在腐生真菌菌株EGS 35-193中被鉴定出来。AaV1有四个基因组双链(ds)RNA片段(dsRNA1 - 4),包装在等轴颗粒中。每个编码链的3'端都有多聚腺苷酸化(36 - 50个核苷酸),但此前尚未研究每个5'端是否存在帽状结构。在此,我们对AaV1基因组进行了表征,发现它在真菌病毒中具有独特特征。我们使用抗帽抗体的RNA斑点印迹法和寡聚帽法证实了AaV1基因组dsRNA的5'端存在帽状结构。针对纯化的AaV1颗粒的多克隆抗体特异性结合一种82kDa的蛋白质,表明该蛋白质是主要衣壳成分。随后的埃德曼降解表明AaV1的dsRNA3片段编码主要衣壳蛋白。两种有缺陷的AaV1 dsRNA2,完整时长2794bp(844个氨基酸),在传代培养过程中出现在EGS 35-193中,这通过逆转录聚合酶链反应(RT-PCR)和Northern杂交得以证实。序列分析表明,两个有缺陷的dsRNA2中的一个在开放阅读框中包含一个231bp的缺失,而另一个在开放阅读框中既有231bp的缺失又有另外465bp的缺失。两个缺失均发生在框内,产生预测的767个氨基酸和612个氨基酸的蛋白质。携带具有缺陷dsRNA2的病毒粒子的真菌分离株生长受损且色素沉着异常。据我们所知,AaV1是首个被鉴定出其基因组片段上同时具有5'帽和3'多聚腺苷酸结构以及dsRNA2特异性缺失的双链RNA病毒。