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通过基因插入或删除相关末端区域序列,生成表达首尔病毒 Gc 糖蛋白的 E3 缺失型犬腺病毒 2。

Generation of E3-deleted canine adenovirus type 2 expressing the Gc glycoprotein of Seoul virus by gene insertion or deletion of related terminal region sequences.

机构信息

College of Veterinary Medicine, South China Agricultural University, 483 Wushan Street, Tianhe District, Guangzhou 510642, Guangdong Province, PR China.

出版信息

J Gen Virol. 2010 Jul;91(Pt 7):1764-71. doi: 10.1099/vir.0.018473-0. Epub 2010 Feb 24.

Abstract

Seoul virus (SEOV) is one of the four hantaviruses known to cause haemorrhagic fever with renal syndrome. The medium genome segment encodes the Gn/Gc glycoproteins of SEOV, which form the major structural part of the virus envelope. Gc and/or Gn are the candidate antigens of hantavirus for induction of a highly immunogenic response for hantavirus vaccine. In this study, the immune response induced by a replication-competent recombinant canine adenovirus type 2 expressing the Gc protein of SEOV was evaluated in BALB/c mice. Sera from immunized mice contained neutralizing antibodies that could specifically recognize SEOV and neutralize its infectivity in vitro. Moreover, the recombinant virus induced complete protection against an intensive infectious challenge with approximately 1000 50 % infective doses for SEOV strain CC-2. Protective-level neutralizing antibodies were maintained for at least 20 weeks. This recombinant virus is therefore a potential alternative to the inactivated vaccine.

摘要

汉城病毒(SEOV)是已知引起肾综合征出血热的四种汉坦病毒之一。中基因组片段编码 SEOV 的 Gn/Gc 糖蛋白,该糖蛋白构成病毒包膜的主要结构部分。Gc 和/或 Gn 是汉坦病毒候选抗原,可诱导汉坦病毒疫苗产生高度免疫应答。在这项研究中,评估了表达 SEOV Gc 蛋白的复制型重组犬腺病毒 2 在 BALB/c 小鼠中诱导的免疫应答。免疫小鼠的血清含有中和抗体,可特异性识别 SEOV 并中和其体外感染性。此外,该重组病毒可完全抵抗大约 1000 个 50%感染剂量的 SEOV 株 CC-2 的密集感染性挑战。保护性中和抗体至少持续 20 周。因此,这种重组病毒是一种替代灭活疫苗的潜在选择。

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