Division of Virology, ICAR-Indian Veterinary Research Institute, Nainital District, Mukteshwar, Uttarakhand, 263138, India.
FMD Research Centre, ICAR-IVRI, Hebbal, Bengaluru, Karnataka, 560024, India.
Virus Genes. 2024 Dec;60(6):642-651. doi: 10.1007/s11262-024-02097-0. Epub 2024 Aug 13.
Orf or contagious ecthyma is a highly contagious, zoonotic, and economically important global viral disease of small ruminants and is endemic in India. Vaccination of susceptible goats/sheep along with suitable recombinant protein-based serological assay will be useful in the control of the infection. In this study, the full-length and truncated versions of F1L encoding gene (ORF 059) of orf virus were cloned into pFasBac HT A vector, transformed in DH10Bac cells, and expressed in insect cells. The full-length and truncated recombinant F1L proteins were expressed as a 6 × histidine-tagged fusion protein for ease of purification by Ni-NTA affinity chromatography under denaturing conditions. A protein with ~ 40 kDa and ~ 35 kDa for full-length and truncated F1L protein, respectively, were expressed and confirmed by SDS-PAGE and western blot. The protein reactivity evaluated by western blot analysis and indirect ELISA using ORFV hyperimmune serum was also found to be reactive. The results of the present study showed that the purified recombinant F1L protein can be used as a diagnostic antigen in sero-surveillance of ORFV infection in small ruminants. To the best of authors' knowledge, this is the first report on the expression of ORFV F1L in insect cells using a baculovirus vector and its successful purification to use as the potential diagnostic antigen in ELISA.
口疮或传染性脓疱性皮炎是一种高度传染性、人畜共患且具有重要经济意义的小反刍动物全球病毒性疾病,在印度流行。对易感山羊/绵羊进行疫苗接种,并结合合适的重组蛋白血清学检测方法,将有助于控制感染。在本研究中,将口疮病毒的全长和截短版本的 F1L 编码基因(ORF059)克隆到 pFasBacHTA 载体中,转化至 DH10Bac 细胞,并在昆虫细胞中表达。全长和截短的重组 F1L 蛋白被表达为 6×组氨酸标记融合蛋白,便于在变性条件下通过 Ni-NTA 亲和层析进行纯化。通过 SDS-PAGE 和 Western blot 鉴定,分别表达并确认了约 40 kDa 和约 35 kDa 的全长和截短 F1L 蛋白。使用 ORFV 高免血清进行 Western blot 分析和间接 ELISA 评估的蛋白反应性也被发现具有反应性。本研究结果表明,纯化的重组 F1L 蛋白可用作小反刍动物 ORFV 感染血清学监测的诊断抗原。据作者所知,这是首次使用杆状病毒载体在昆虫细胞中表达 ORFV F1L 并成功进行纯化,可作为 ELISA 中的潜在诊断抗原。