文献类型: 外文期刊
作者: Chen, Sha 1 ; Jiang, Guangzhuang 1 ; Wu, Jianxiang 1 ; Liu, Yong 3 ; Qian, Yajuan 1 ; Zhou, Xueping 1 ;
作者机构: 1.Zhejiang Univ, Inst Biotechnol, Hangzhou 310058, Zhejiang, Peoples R China
2.Chinese Acad Agr Sci, Inst Plant Protect, State Key Lab Biol Plant Dis & Insect Pests, Beijing 100193, Peoples R China
3.Hunan Acad Agr Sci, Hunan Plant Protect Inst, Key Lab Pest Management Hort Crop Hunan Prov, Changsha 410125, Hunan, Peoples R China
关键词: Maize yellow mosaic virus;deep sequencing;infectious clone;suppressor;molecular variation;sRNA
期刊名称:VIRUSES-BASEL ( 影响因子:5.048; 五年影响因子:5.127 )
ISSN: 1999-4915
年卷期: 2016 年 8 卷 5 期
页码:
收录情况: SCI
摘要: A novel virus, tentatively named Maize Yellow Mosaic Virus (MaYMV), was identified from the field-grown maize plants showing yellow mosaic symptoms on the leaves collected from the Yunnan Province of China by the deep sequencing of small RNAs. The complete 5642 nucleotide (nt)-long genome of the MaYMV shared the highest nucleotide sequence identity (73%) to Maize Yellow Dwarf Virus-RMV. Sequence comparisons and phylogenetic analyses suggested that MaYMV represents a new member of the genus Polerovirus in the family Luteoviridae. Furthermore, the P0 protein encoded by MaYMV was demonstrated to inhibit both local and systemic RNA silencing by co-infiltration assays using transgenic Nicotiana benthamiana line 16c carrying the GFP reporter gene, which further supported the identification of a new polerovirus. The biologically-active cDNA clone of MaYMV was generated by inserting the full-length cDNA of MaYMV into the binary vector pCB301. RT-PCR and Northern blot analyses showed that this clone was systemically infectious upon agro-inoculation into N. benthamiana. Subsequently, 13 different isolates of MaYMV from field-grown maize plants in different geographical locations of Yunnan and Guizhou provinces of China were sequenced. Analyses of their molecular variation indicate that the 3 half of P3-P5 read-through protein coding region was the most variable, whereas the coat protein- (CP-) and movement protein- (MP-)coding regions were the most conserved.
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