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NDV 融合蛋白的 DI-DII 连接区突变赋予了血凝素-神经氨酸酶非依赖性的细胞融合促进作用。

Mutations in the DI-DII linker of the NDV fusion protein conferred hemagglutinin-neuraminidase-independent cell fusion promotion.

机构信息

1 Department of Virology, School of Public Health, Shandong University, Jinan 250012, PR China.

2 Department of Laboratory Medicine, Shandong Provincial Qianfoshan Hospital, Shandong University, Jinan 250014, PR China.

出版信息

J Gen Virol. 2019 Jun;100(6):958-967. doi: 10.1099/jgv.0.001278. Epub 2019 May 29.

DOI:10.1099/jgv.0.001278
PMID:31140969
Abstract

Newcastle disease (ND), which is caused by Newcastle disease virus (NDV), is a highly contagious disease in chickens and is a great threat to the poultry industry. Fusion of the viral and target cell membranes is a prerequisite for NDV's entry into host cells. This process is directly mediated by the fusion (F) protein. Although several domains of F are known to regulate membrane fusion activity, the roles of the DI-DII linker (residues 376-381) of the NDV F protein in membrane fusion still remain unclear. To investigate the roles of this linker in NDV F-induced cell-cell fusion, mutations were engineered into this linker by site-directed mutagenesis. These mutants were analysed with respect to cell surface expression and membrane fusion activity. Each of the mutated F proteins in this linker was expressed at the cell surface at a similar level to wild-type (WT) F. However, most of them resulted in significant alterations in fusion activity. In particular, the mutants G377S, A378D, L379A and T380P were able to independently mediate cell fusion in the absence of HN protein in BHK-21 cells. Taken together, the results indicated that the DI-DII linker region has an important effect on the fusion activity of NDV F and mutants in this region could alter the requirement for HN for the promotion of membrane fusion.

摘要

新城疫(ND)是由新城疫病毒(NDV)引起的一种高度传染性疾病,对家禽业构成巨大威胁。病毒和靶细胞膜的融合是 NDV 进入宿主细胞的前提。这一过程直接由融合(F)蛋白介导。尽管已知 F 蛋白的几个结构域调节膜融合活性,但 NDV F 蛋白的 DI-DII 连接区(残基 376-381)在膜融合中的作用仍不清楚。为了研究该连接区在 NDV F 诱导的细胞-细胞融合中的作用,通过定点诱变工程对该连接区进行了突变。对这些突变体进行了细胞表面表达和膜融合活性分析。该连接区中的每个突变 F 蛋白在细胞表面的表达水平与野生型(WT)F 相似。然而,它们中的大多数导致融合活性发生显著改变。特别是,突变体 G377S、A378D、L379A 和 T380P 能够在没有 BHK-21 细胞中 HN 蛋白的情况下独立介导细胞融合。总之,结果表明 DI-DII 连接区对 NDV F 的融合活性有重要影响,该区域的突变体可能改变 HN 促进膜融合的需求。

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引用本文的文献

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2
Direct interaction of the molecular chaperone GRP78/BiP with the Newcastle disease virus hemagglutinin-neuraminidase protein plays a vital role in viral attachment to and infection of culture cells.分子伴侣 GRP78/BiP 与新城疫病毒血凝素-神经氨酸酶蛋白的直接相互作用在病毒附着和感染培养细胞中起着至关重要的作用。
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Adaptor complex-mediated trafficking of Newcastle disease virus fusion protein is regulated by the YLMY motif of its cytoplasmic tail.
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