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来自巴基斯坦分离株的新型维克托病毒,缺乏典型的翻译终止/起始序列特征。

Novel Victorivirus from a Pakistani Isolate of Lacking a Typical Translational Stop/Restart Sequence Signature.

机构信息

Institute of Plant Science and Resources, Okayama University, Chuou 2-20-1, Kurashiki, Okayama 710-0046, Japan.

Crop Diseases Research Institute, National Agricultural Research Centre, Park Road, Islamabad 45500, Pakistan.

出版信息

Viruses. 2019 Jun 25;11(6):577. doi: 10.3390/v11060577.

Abstract

The family currently contains five genera , , , , and . Members in this family generally have a set of two-open reading frame (ORF) elements in their genome with the 5'-proximal ORF (ORF1) encoding a capsid protein (CP) and the 3'-proximal one (ORF2) for RNA-dependent RNA polymerase (RdRp). How the downstream open reading frames (ORFs) are expressed is genus-specific. All victoriviruses characterized thus far appear to use the stop/restart translation mechanism, allowing for the expression of two separate protein products from bicitronic genome-sized viral mRNA, while the totiviruses use a -1 ribosomal frame-shifting that leads to a fusion product of CP and RdRp. We report the biological and molecular characterization of a novel victorivirus termed Alternaria alternata victorivirus 1 (AalVV1) isolated from in Pakistan. The phylogenetic and molecular analyses showed AalVV1 to be distinct from previously reported victoriviruses. AalVV1 appears to have a sequence signature required for the -1 frame-shifting at the ORF1/2 junction region, rather than a stop/restart key mediator. By contrast, SDS-polyacrylamide gel electrophoresis and peptide mass fingerprinting analyses of purified virion preparations suggested the expression of two protein products, not a CP-RdRp fusion product. How these proteins are expressed is discussed in this study. Possible effects of infection by this virus were tested in two fungal species: and RNA silencing proficient and deficient strains of , a model filamentous fungus. AalVV1 showed symptomless infection in all of these fungal strains, even in the RNA silencing deficient strain.

摘要

该家族目前包含五个属,即、、、和。该家族的成员通常在其基因组中有一组两个开放阅读框(ORF)元件,其中 5'-近端 ORF(ORF1)编码衣壳蛋白(CP),3'-近端 ORF(ORF2)编码 RNA 依赖性 RNA 聚合酶(RdRp)。下游开放阅读框(ORFs)的表达方式因属而异。迄今为止,所有已鉴定的 victoriviruses 似乎都使用停止/重新启动翻译机制,允许从双顺反子基因组大小的病毒 mRNA 表达两种单独的蛋白产物,而 totiviruses 使用 -1 核糖体移码,导致 CP 和 RdRp 的融合产物。我们报告了一种新型 victorivirus 的生物学和分子特征,该病毒称为 Alternaria alternata victorivirus 1(AalVV1),从巴基斯坦的分离得到。系统发育和分子分析表明,AalVV1 与先前报道的 victoriviruses 不同。AalVV1 似乎具有在 ORF1/2 交界处进行 -1 框移的序列特征,而不是停止/重新启动关键介质。相比之下,通过 SDS-聚丙烯酰胺凝胶电泳和纯化病毒粒子制剂的肽质量指纹分析表明,表达了两种蛋白产物,而不是 CP-RdRp 融合产物。本研究讨论了这些蛋白的表达方式。在两种真菌物种中测试了这种病毒感染的可能影响:和 RNA 沉默有效的和缺乏的,丝状真菌模型。AalVV1 在所有这些真菌菌株中均表现出无症状感染,甚至在 RNA 沉默缺乏的 菌株中也是如此。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9de/6631646/37a237b04d3c/viruses-11-00577-g001.jpg

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