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首页> 外文期刊>Archives of virology >Deep sequencing of dsRNAs recovered from mosaic-diseased pigeonpea reveals the presence of a novel emaravirus: pigeonpea sterility mosaic virus 2
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Deep sequencing of dsRNAs recovered from mosaic-diseased pigeonpea reveals the presence of a novel emaravirus: pigeonpea sterility mosaic virus 2

机译:从花叶病的木豆中回收的dsRNA的深度测序揭示了新型埃马病毒的存在:木豆不育花叶病毒2

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Deep-sequencing analysis of double-stranded RNA extracted from a mosaic-diseased pigeonpea plant (Cajanus cajan L., family Fabaceae) revealed the complete sequence of six emaravirus-like negative-sense RNA segments of 7009, 2229, 1335, 1491, 1833 and 1194 nucleotides in size. In the order from RNA1 to RNA6, these genomic RNAs contained ORFs coding for the RNA-dependent RNA polymerase (RdRp, p1 of 266 kDa), the glycoprotein precursor (GP, p2 of 74.5 kDa), the nucleocapsid (NC, p3 of 34.9 kDa), and the putative movement protein (MP, p4 of 40.7 kDa), while p5 (55 kDa) and p6 (27 kDa) had unknown functions. All RNA segments showed distant relationships to viruses of the genus Emaravirus, and in particular to pigeonpea sterility mosaic virus (PPSMV), with which they shared nucleotide sequence identity ranging from 48.5 % (RNA3) to 62.5 % (RNA1). In phylogenetic trees constructed from the sequences of the proteins encoded by RNA1, RNA2 and RNA3 (p1, p2 and p3), this new viral entity showed a consistent grouping with fig mosaic virus (FMV) and rose rosette virus (RRV), which formed a cluster of their own, clearly distinct from PPSMV-1. In experimental greenhouse trials, this novel virus was successfully transmitted to pigeonpea and French bean seedlings by the eriophyid mite Aceria cajani. Preliminary surveys conducted in the Hyderabad region (India) showed that the virus in question is widespread in pigeonpea plants affected by sterility mosaic disease (86.4 %) but is absent in symptomless plants. Based on molecular, biological and epidemiological features, this novel virus is the second emaravirus infecting pigeonpea, for which the provisional name pigeonpea sterility mosaic virus 2 (PPSMV-2) is proposed.
机译:从花叶病的木豆植物(Cajanus cajan L.,Fabaceae家族)提取的双链RNA的深度测序分析揭示了六个真丝病毒样负义RNA片段的完整序列,分别为7009、2229、1335、1491、1833和1194个核苷酸的大小。从RNA1到RNA6的顺序,这些基因组RNA包含编码RNA依赖性RNA聚合酶(RdRp,p1为266 kDa),糖蛋白前体(GP,p2为74.5 kDa),核壳(NC,p3为34.9)的ORF。 kDa)和假定的运动蛋白(MP,p4为40.7 kDa),而p5(55 kDa)和p6(27 kDa)的功能未知。所有RNA片段均与Emaravirus属病毒,特别是与木豆不育花叶病毒(PPSMV)有着遥远的关系,它们共享的核苷酸序列同一性范围为48.5%(RNA3)至62.5%(RNA1)。在由RNA1,RNA2和RNA3(p1,p2和p3)编码的蛋白质序列构成的系统发育树中,这种新的病毒实体与无花果花叶病毒(FMV)和玫瑰玫瑰花病毒(RRV)保持一致的分组,自己的集群,明显不同于PPSMV-1。在温室实验中,这种新型病毒已被螨虫Aceria cajani成功地传播到了木豆和菜豆的幼苗。在海得拉巴地区(印度)进行的初步调查显示,所讨论的病毒在受不育花叶病影响的木豆植物中广泛分布(86.4%),而在无症状植物中则没有。基于分子,生物学和流行病学特征,该新型病毒是第二种感染木豆的真核病毒,为此提出了临时名称木豆不育性花叶病毒2(PPSMV-2)。

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