Institute of Preventive Veterinary Medicine, Sichuan Agricultural University, Wenjiang, Chengdu City, Sichuan 611130, P.R. China.
Virol J. 2011 Aug 24;8:413. doi: 10.1186/1743-422X-8-413.
Previous studies have indicated that the UL16 protein and its homologs from herpesvirus were conserved and played similar roles in viral DNA packaging, virion assembly, budding, and egress. However, there was no report on the UL16 gene product of duck enteritis virus (DEV). In this study, we analyzed the amino acid sequence of UL16 using bioinformatics tools and expressed in Escherichia coli Rosetta (DE3) induced by isopropy1-β-D-thiogalactopyranoside (IPTG). The recombinant protein was produced, purified using a Ni-NTA column and used to generate the polyclonal antibody against UL16. The intracellular distribution of the DEV UL16 product was carried out using indirect immunofluorescence assay.
In our study, UL16 gene of DEV was composed of 1089 nucleotides, which encoded 362 amino acids. Multiple sequence alignment suggested that the UL16 gene was highly conserved in herpesvirus family. The UL16 gene was cloned into a pET prokaryotic expression vector and transformed into Escherichia coli Rossetta (DE3) induced by IPTG. A 60kDa fusion protein band corresponding to the predicted size was produced on the SDS-PAGE, purified using a Ni-NTA column. Anti-UL16 polyclonal sera was prepared by immunizing rabbits, and reacted with a band in the IPTG induced cell lysates with an apparent molecular mass of 60 kDa. In vivo expression of the UL16 protein in DEV infected duck embryo fibroblast cells (DEFs) was localized mostly around perinuclear cytoplasmic area and in cytosol using indirect immunofluorescence assay.
The UL16 gene of DEV was successfully cloned, expressed and detected in DEV infected DEFs for the first time. The UL16 protein localized mostly around perinuclear cytoplasmic area and in cytosol in DEV infected DEFs. DEV UL16 shared high similarity with UL16 family members, indicating that DEV UL16 many has similar function with its homologs. All these results may provide some insight for further research about full characterizations and functions of the DEV UL16.
先前的研究表明,疱疹病毒的 UL16 蛋白及其同源物在病毒 DNA 包装、病毒粒子组装、出芽和逸出中具有保守性,发挥相似的作用。然而,关于鸭肠炎病毒 (DEV) 的 UL16 基因产物尚无报道。在本研究中,我们使用生物信息学工具分析了 UL16 的氨基酸序列,并通过异丙基-β-D-硫代半乳糖吡喃糖苷 (IPTG) 诱导大肠杆菌 Rosetta (DE3) 进行表达。使用 Ni-NTA 柱对重组蛋白进行了纯化,并用于产生针对 UL16 的多克隆抗体。通过间接免疫荧光法进行了 DEV UL16 产物的细胞内分布。
在本研究中,DEV 的 UL16 基因由 1089 个核苷酸组成,编码 362 个氨基酸。多重序列比对表明,疱疹病毒家族中的 UL16 基因高度保守。将 UL16 基因克隆到 pET 原核表达载体中,并通过 IPTG 诱导大肠杆菌 Rosetta (DE3) 进行转化。在 SDS-PAGE 上产生了与预测大小相对应的 60kDa 融合蛋白带,使用 Ni-NTA 柱进行了纯化。通过免疫兔子制备了抗 UL16 多克隆血清,并与 IPTG 诱导的细胞裂解物中的 60kDa 明显分子量的条带反应。通过间接免疫荧光法,在 DEV 感染的鸭胚成纤维细胞 (DEF) 中,UL16 蛋白在体内表达主要定位于核周细胞质区和细胞质中。
首次成功克隆、表达和检测了 DEV 的 UL16 基因,在 DEV 感染的 DEF 中。在 DEV 感染的 DEF 中,UL16 蛋白主要定位于核周细胞质区和细胞质中。DEV UL16 与 UL16 家族成员高度相似,表明 DEV UL16 可能具有与其同源物相似的功能。所有这些结果可能为进一步研究 DEV UL16 的全面特征和功能提供一些启示。