Zhang Wenting, Cai Chengzhi, Lin Li, Tao Yizhi Jane, Jin Meilin
State Key Laboratory of Agricultural Microbiology, College of Veterinary Medicine, Huazhong Agricultural University, Wuhan, 430070, People's Republic of China.
Department of Aquatic Animal Medicine, College of Fisheries, Huazhong Agricultural University, Wuhan, Hubei, 430070, China.
Virol J. 2017 Feb 15;14(1):30. doi: 10.1186/s12985-017-0702-z.
Infectious salmon anemia virus (ISAV) is an important fish pathogen that causes high mortality in farmed Atlantic salmon. The ISAV genome consists of eight single-stranded, negative-sense RNA segments. The six largest segments contain one open reading frame (ORF) each, and encode three polymerase proteins, nucleoprotein, fusion protein, and hemagglutinin esterase protein. The two smallest segments contain more than one ORF each. The segment 7 encodes non-structural protein 1 (NS1) and nuclear export protein (NEP), while segment 8 encodes matrix protein 1 and 2 (M1 and M2). NS1 and M2 have been well known as antagonist of type I interferon. However, little is known about the characterization of M1 or NEP. In addition, heat shock cognate 70 (Hsc70) has been reported to interact with M1 and NEP of influenza viruses for the export of viral ribonucleoprotein (vRNP) via vRNP-M1-NEP complex, the goal of this study therefore was to characterize the subcellular localization and interactions of ISAV M1 and NEP as well as cellular Hsc70.
When M1, NEP, and Hsc70 were individually expressed in the stripped snakehead (SSN-1) cells, we found that M1 protein was localized in both cytosol and nucleus of the cells, NEP was localized only in the cytosol and accumulated adjacent to the nucleus, while Hsc70 was localized throughout the cytosol, but not in the nucleus. However, when two of them were co-expressed, we found that both M1 and Hsc70 were co-localized with NEP in the cytosol and accumulated adjacent to the nucleus, while M1 and Hsc70 were still localized as they were expressed individually. Furthermore, pull-down assay was performed and showed that NEP could interact with both M1 and Hsc70, and M1-Hsc70 interaction was also observed although the interaction was weaker than that of NEP-Hsc70.
Our study characterized the subcellular localization and interactions of three proteins including M1 and NEP of ISAV, and Hsc70. These data will help towards a better understanding of the life cycle of ISAV, especially the process of vRNP export.
传染性鲑鱼贫血病毒(ISAV)是一种重要的鱼类病原体,可导致养殖大西洋鲑鱼的高死亡率。ISAV基因组由八个单链、负义RNA片段组成。六个最大的片段各包含一个开放阅读框(ORF),并编码三种聚合酶蛋白、核蛋白、融合蛋白和血凝素酯酶蛋白。两个最小的片段各包含一个以上的ORF。片段7编码非结构蛋白1(NS1)和核输出蛋白(NEP),而片段8编码基质蛋白1和2(M1和M2)。NS1和M2一直被认为是I型干扰素的拮抗剂。然而,关于M1或NEP的特性知之甚少。此外,据报道热休克同源蛋白70(Hsc70)通过vRNP-M1-NEP复合物与流感病毒的M1和NEP相互作用,以促进病毒核糖核蛋白(vRNP)的输出,因此本研究的目的是表征ISAV M1和NEP以及细胞Hsc70的亚细胞定位和相互作用。
当M1、NEP和Hsc70分别在条纹鳢(SSN-1)细胞中表达时,我们发现M1蛋白定位于细胞的细胞质和细胞核中,NEP仅定位于细胞质中并在细胞核附近积累,而Hsc70定位于整个细胞质中,但不在细胞核中。然而,当其中两者共表达时,我们发现M1和Hsc70都与NEP在细胞质中共定位并在细胞核附近积累,而M1和Hsc70仍保持其单独表达时的定位。此外,进行了下拉实验,结果表明NEP可以与M1和Hsc70相互作用,并且还观察到M1-Hsc70相互作用,尽管该相互作用比NEP-Hsc70的相互作用弱。
我们的研究表征了包括ISAV的M1和NEP以及Hsc70在内的三种蛋白质的亚细胞定位和相互作用。这些数据将有助于更好地理解ISAV的生命周期,特别是vRNP输出过程。