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The interaction between the Nipah virus nucleocapsid protein and phosphoprotein regulates virus replication

机译:Nipah病毒核衣壳蛋白和磷蛋白之间的相互作用调节病毒复制

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摘要

Continued outbreaks of Henipaviruses in South Asia and Australia cause severe and lethal disease in both humans and animals. Together, with evidence of human to human transmission for Nipah virus and the lack of preventative or therapeutic measures, its threat to cause a widespread outbreak and its potential for weaponization has increased. In this study we demonstrate how overexpression of the Nipah virus nucleocapsid protein regulates viral polymerase activity and viral RNA production. By overexpressing the Nipah virus nucleocapsid protein in trans viral transcription was inhibited; however, an increase in viral genome synthesis was observed. Together, the bias of polymerase activity towards genome production led to the severe inhibition of viral progeny. We identified two domains within the nucleocapsid protein, which were each independently capable of binding the viral phosphoprotein. Evident by our data, we propose that the nucleocapsid protein’s ability to interact with the phosphoprotein of the polymerase complex causes a change in polymerase activity and subsequent deficiency in viral replication. This study not only provides insights into the dynamics of Henipavirus RNA synthesis and replication, but also provides insight into potential targets for antiviral drug development.
机译:南亚和澳大利亚持续爆发的猪瘟病毒会在人类和动物中引起严重的致命疾病。加上人为传播尼帕病毒的证据以及缺乏预防或治疗措施的证据,其造成广泛爆发的威胁和武器化的潜力有所增加。在这项研究中,我们证明了尼帕病毒核衣壳蛋白的过表达如何调节病毒聚合酶活性和病毒RNA产生。通过过表达尼帕病毒核衣壳蛋白,反式病毒转录受到抑制;然而,观察到病毒基因组合成的增加。在一起,聚合酶活性偏向基因组生产导致病毒后代的严重抑制。我们确定了核衣壳蛋白内的两个域,每个域独立地能够结合病毒磷蛋白。根据我们的数据,我们认为核衣壳蛋白与聚合酶复合物的磷酸蛋白相互作用的能力会引起聚合酶活性的改变以及随后病毒复制的缺陷。这项研究不仅提供了对Henipavirus RNA合成和复制动力学的见解,而且还提供了对抗病毒药物开发的潜在靶标的见解。

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