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三种葡萄病毒在植物中的增殖差异可能解释它们在葡萄园中的发病率。

Differences of Three Ampeloviruses' Multiplication in Plant May Explain Their Incidences in Vineyards.

作者信息

Velasco Leonardo, Bota Josefina, Montero Rafael, Cretazzo Enrico

机构信息

Instituto Andaluz de Investigación y Formación Agraria, Pesquera, Alimentaria y de la Producción Ecológica (IFAPA), 29140 Churriana, Málaga, Spain.

Institut de Recerca i Formació Agrària i Pesquera de les Illes Balears, 07009 Palma de Mallorca, Spain.

出版信息

Plant Dis. 2014 Mar;98(3):395-400. doi: 10.1094/PDIS-04-13-0433-RE.

Abstract

Grapevine leafroll ampeloviruses have been recently grouped into two major clades, one for Grapevine leafroll associated virus (GLRaV) 1 and 3 and another one grouping GLRaV-4 and its variants. In order to understand biological factors mediating differential ampelovirus incidences in vineyards, quantitative real-time polymerase chain reactions were performed to assess virus populations in three grapevine varieties in which different infection status were detected: GLRaV-3 + GLRaV-4, GLRaV-3 + GLRaV-4 strain 5, and GLRaV-4 alone. Specific primers based on the RNA-dependent RNA polymerase (RdRp) domains of GLRaV-3, GLRaV-4, and GLRaV-4 strain 5 were used. Absolute and relative quantitations of the three viruses were achieved by normalization of data to the concentration of the endogenous gene actin. In spring, the populations of GLRaV-4 and GLRaV-4 strain 5 were 1.7 × 10 to 5.0 × 10 genomic RNA copies/mg of petiole tissue whereas, for GLRaV-3, values were significantly higher, ranging from 5.6 × 10 and 1.0 × 10 copies mg. In autumn, GLRaV-4 and GLRaV-4 strain 5 populations increased significantly, displaying values for genome copies between 4.1 × 10 and 6.3 × 10 copies mg, whereas GLRaV-3 populations displayed a less pronounced boost but were still significantly higher, ranging from 4.1 × 10 to 1.6 × 10 copies mg. To investigate whether additional viruses may interfere in the quantifications the small RNA populations, vines were analyzed by Ion Torrent high-throughput sequencing. It allowed the identification of additional viruses and viroids, including Grapevine virus A, Hop stunt viroid, Grapevine yellow speckle viroid 1, and Australian grapevine viroid. The significance of these findings is discussed.

摘要

葡萄卷叶病毒属病毒最近被分为两个主要进化枝,一个包含葡萄卷叶相关病毒1(GLRaV-1)和葡萄卷叶相关病毒3(GLRaV-3),另一个包含葡萄卷叶相关病毒4(GLRaV-4)及其变种。为了了解介导葡萄园不同葡萄卷叶病毒发生率的生物学因素,进行了定量实时聚合酶链反应,以评估在检测到不同感染状态的三个葡萄品种中的病毒种群:GLRaV-3 + GLRaV-4、GLRaV-3 + GLRaV-4菌株5和单独的GLRaV-4。使用了基于GLRaV-3、GLRaV-4和GLRaV-4菌株5的RNA依赖性RNA聚合酶(RdRp)结构域的特异性引物。通过将数据归一化到内源性基因肌动蛋白的浓度,实现了三种病毒的绝对定量和相对定量。春季,GLRaV-4和GLRaV-4菌株5的种群数量为每毫克叶柄组织1.7×10至5.0×10个基因组RNA拷贝,而GLRaV-3的值显著更高,范围为5.6×10至1.0×10个拷贝/毫克。秋季,GLRaV-4和GLRaV-4菌株5的种群数量显著增加,基因组拷贝数在4.1×10至6.3×10个拷贝/毫克之间,而GLRaV-3的种群数量增加不太明显,但仍然显著更高,范围为4.1×10至1.6×10个拷贝/毫克。为了研究是否有其他病毒可能干扰小RNA种群的定量,通过Ion Torrent高通量测序对葡萄藤进行了分析。这使得能够鉴定出其他病毒和类病毒,包括葡萄病毒A、啤酒花矮化类病毒、葡萄黄斑类病毒1和澳大利亚葡萄类病毒。讨论了这些发现的意义。

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