Department of Agricultural Biotechnology, National Institute of Genetic Engineering and Biotechnology (NIGEB), Shahrake- Pajoohesh Blvd., 15th Km, Tehran-Karaj Highway, P.O. Box 14965-161, Tehran, Iran.
Department of Molecular Biology and Genetic Engineering, Stem Cell Research Center, Tehran, Iran.
Transgenic Res. 2022 Apr;31(2):201-213. doi: 10.1007/s11248-021-00295-2. Epub 2022 Jan 10.
Newcastle disease virus (NDV) is a lethal virus in avian species with a disastrous effect on the poultry industry. NDV is enveloped by a host-derived membrane with two glycosylated haemagglutinin-neuraminidase (HN) and Fusion (F) proteins. NDV infection usually leads to death within 2-6 days, so the preexisting antibodies provide the most critical protection for this infection. The HN and F glycoproteins are considered the main targets of the immune system. In the present study, two constructs harboring the HN or F epitopes are sub-cloned separately under the control of a root-specific promoter NtREL1 or CaMV35S (35S Cauliflower Mosaic Virus promoter) as a constitutive promoter. The recombinant vectors were transformed into the Agrobacterium tumefaciens strain LBA4404 and then introduced to tobacco (Nicotiana tabacum L.) leaf disk explants. PCR with specific primers was performed to confirm the presence of the hn and f genes in the genome of the regenerated plants. Then, the positive lines were transformed via non-recombinant A. rhizogenes (strain ATCC15834) to develop hairy roots.HN and F were expressed at 0.37% and 0.33% of TSP using the CaMV35S promoter and at 0.75% and 0.54% of TSP using the NtREL1 promoter, respectively. Furthermore, the mice fed transgenic hairy roots showed a high level of antibody responses (IgG and IgA) against rHN and rF proteins.
新城疫病毒(NDV)是一种对禽类具有致命性的病毒,对家禽业造成了灾难性的影响。NDV 被宿主衍生的膜所包裹,膜上有两种糖基化的血凝素-神经氨酸酶(HN)和融合(F)蛋白。NDV 感染通常会导致 2-6 天内死亡,因此预先存在的抗体是这种感染的最关键保护。HN 和 F 糖蛋白被认为是免疫系统的主要靶标。在本研究中,两个分别携带 HN 或 F 表位的构建体在根特异性启动子 NtREL1 或 CaMV35S(35S 花椰菜花叶病毒启动子)的控制下被亚克隆,作为组成型启动子。重组载体被转化到根癌农杆菌菌株 LBA4404 中,然后引入烟草(Nicotiana tabacum L.)叶盘外植体。使用特异性引物进行 PCR 以确认再生植物基因组中 hn 和 f 基因的存在。然后,通过非重组农杆菌(菌株 ATCC15834)将阳性系转化以产生发根。使用 CaMV35S 启动子,HN 和 F 的表达量分别为总可溶性蛋白的 0.37%和 0.33%,使用 NtREL1 启动子,HN 和 F 的表达量分别为总可溶性蛋白的 0.75%和 0.54%。此外,喂食转基根的小鼠表现出针对 rHN 和 rF 蛋白的高抗体反应(IgG 和 IgA)。