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鉴定感染香蕉束顶病毒的香蕉细胞中的类病毒体。

Identification of putative viroplasms within banana cells infected by banana streak MY virus.

机构信息

Queensland Alliance for Agriculture and Food Innovation, The University of Queensland, St. Lucia 4072, Queensland, Australia.

Centre for Microscopy and Microanalysis, The University of Queensland, St. Lucia 4072, Queensland, Australia.

出版信息

J Gen Virol. 2020 Dec;101(12):1305-1312. doi: 10.1099/jgv.0.001498. Epub 2020 Oct 1.

Abstract

The badnavirus replication cycle is poorly understood and most knowledge is based on extrapolations from model viruses such as (CaMV). However, in contrast to CaMV, badnaviruses are thought not to produce viroplasms and therefore it has been a mystery as to where virion assembly occurs. In this study, ultrathin sections of a banana leaf infected with a badnavirus, banana streak MY virus (BSMYV), were examined by transmission electron microscopy. Electron-dense inclusion bodies (EDIBs) were sporadically distributed in parenchymatous tissues of the leaf, most commonly in the palisade and spongy mesophyll cells. These EDIBs had a characteristic structure, comprising an electron-dense core, a single, encircling lacuna and an outer ring of electron-dense material. However, much less frequently, EDIBs with two or three lacunae were observed. In the outer ring, densely packed virions were visible with a shape and size consistent with that expected for badnaviruses. Immunogold labelling was done with primary antibodies that detected the N-terminus of the capsid protein and strong labelling of the outer ring but not the central core or lacuna was observed. It is concluded that the EDIBs that were observed are equivalent in function to the viroplasms of CaMV, although obviously different in composition as there is not a paralogue of the transactivation/viroplasm protein in the badnavirus genome. It is postulated that production of a viroplasm could be a conserved characteristic of all members of the .

摘要

双生病毒复制周期的了解甚少,大多数知识都是基于对模式病毒(如 CaMV)的推断得出的。然而,与 CaMV 不同的是,双生病毒被认为不会产生病毒质体,因此病毒体组装发生的位置一直是个谜。在这项研究中,通过透射电子显微镜检查了感染双生病毒香蕉条纹 MY 病毒(BSMYV)的香蕉叶片的超薄切片。电子致密包含体(EDIBs)在叶片的薄壁组织中散在分布,最常见于栅栏组织和海绵状叶肉细胞中。这些 EDIBs 具有特征性结构,包括电子致密核心、单个环绕的腔和电子致密物质的外环。然而,观察到具有两个或三个腔的 EDIBs 的情况要少得多。在外环中,可以看到排列紧密的病毒体,其形状和大小与双生病毒一致。用检测衣壳蛋白 N 端的初级抗体进行免疫金标记,观察到外环强烈标记,但核心或腔均未标记。因此可以得出结论,观察到的 EDIBs 在功能上与 CaMV 的病毒质体相当,尽管它们在组成上明显不同,因为在双生病毒基因组中没有转激活/病毒质体蛋白的类似物。推测产生病毒质体可能是所有 成员的保守特征。

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