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

机译:缺乏典型的翻译停止/重新启动序列签名从巴基斯坦交链孢霉的巴基斯坦分离株的新型病毒。

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摘要

The family Totiviridae currently contains five genera Totivirus, Victorivirus, Leishmavirus, Trichomonasvirus, and Giardiavirus. 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 Alternaria alternata 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: A. alternata and RNA silencing proficient and deficient strains of Cryphonectria parasitica, a model filamentous fungus. AalVV1 showed symptomless infection in all of these fungal strains, even in the RNA silencing deficient C. parasitica strain.
机译:Totiviridae家族目前包含5种Totivirus,Victorivirus,Leishmavirus,Trichomonasvirus和Giardiavirus。这个家族的成员在其基因组中通常具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),而3'-近端一个ORF2(RNA)依赖性RNA聚合酶(RdRp)。下游开放阅读框(ORF)的表达方式是属特定的。到目前为止,所有特征性的杯状病毒似乎都使用了终止/重新启动翻译机制,可以表达双基因组基因组大小的病毒mRNA中的两种分离的蛋白质产物,而犬病毒则使用-1核糖体移码,从而产生了融合产物。 CP和RdRp。我们报告了分离自巴基斯坦链格孢的一种新的维克多病毒的生物学和分子表征,该病毒被称为链格孢病毒1(AalVV1)。系统发育和分子分析表明,AalVV1与以前报道的病毒有所不同。 AalVV1似乎具有在ORF1 / 2接合区域进行-1移码所需的序列签名,而不是停止/重新启动关键介体。相比之下,纯化的病毒体制剂的SDS-聚丙烯酰胺凝胶电泳和肽质量指纹分析表明,两种蛋白质产物的表达,而不是CP-RdRp融合产物。在这项研究中讨论了这些蛋白质如何表达。在两种真菌物种中测试了这种病毒感染的可能影响:交替链霉菌和RNA沉默的寄生丝para真菌Cryphonectria parasitica的品系。 AalVV1在所有这些真菌菌株中均表现出无症状感染,即使在RNA沉默缺陷的寄生寄生梭状芽胞杆菌菌株中也是如此。

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