Xu Bangfeng, Liu Xingpo, Yan Dawei, Teng Qiaoyang, Yuan Chunxiu, Zhang Zhifei, Liu Qinfang, Li Zejun
Department of Avian Infectious Diseases, Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Shanghai, China.
Front Microbiol. 2023 Jun 22;14:1140141. doi: 10.3389/fmicb.2023.1140141. eCollection 2023.
Since its outbreak in 2010, Tembusu virus (TMUV) has spread widely throughout China and Southeast Asia, causing significant economic losses to the poultry industry. In 2018, an attenuated vaccine called FX2010-180P (180P) was licensed for use in China. The 180P vaccine has demonstrated its immunogenicity and safety in mice and ducks. The potential use of 180P as a backbone for flavivirus vaccine development was explored by replacing the pre-membrane (prM) and envelope (E) genes of the 180P vaccine strain with those of Japanese encephalitis virus (JEV). Two chimeric viruses, 180P/JEV-prM-E and 180P/JEV-prM-E with an additional E protein S156P mutation were successfully rescued and characterized. Growth kinetics studies showed that the two chimeric viruses replicated to similar titers as the parental 180P virus in cells. Animal studies also revealed that the virulence and neuroinvasiveness of the 180P/JEV-prM-E chimeric virus was decreased in mice inoculated intracerebrally (i.c.) and intranasally (i.n.), respectively, compared to the wild-type JEV strain. However, the chimeric 180P/JEV-prM-E virus was still more virulent than the parent 180P vaccine in mice. Additionally, the introduction of a single E mutation in the chimeric virus 180P/JEV-prM-E further attenuated the virus, which provided complete protection against challenge with a virulent JEV strain in the mouse model. These results indicated that the FX2010-180P could be used as a promising backbone for flavivirus vaccine development.
自2010年爆发以来,坦布苏病毒(TMUV)已在中国和东南亚广泛传播,给家禽业造成了重大经济损失。2018年,一种名为FX2010 - 180P(180P)的减毒疫苗在中国获得许可使用。180P疫苗已在小鼠和鸭中证明了其免疫原性和安全性。通过用日本脑炎病毒(JEV)的前膜(prM)和包膜(E)基因替换180P疫苗株的相应基因,探索了180P作为黄病毒疫苗开发骨架的潜在用途。成功拯救并鉴定了两种嵌合病毒,即180P/JEV - prM - E和具有额外E蛋白S156P突变的180P/JEV - prM - E。生长动力学研究表明,这两种嵌合病毒在细胞中的复制滴度与亲本180P病毒相似。动物研究还显示,与野生型JEV株相比,180P/JEV - prM - E嵌合病毒在分别经脑内(i.c.)和鼻内(i.n.)接种的小鼠中的毒力和神经侵袭性降低。然而,嵌合的180P/JEV - prM - E病毒在小鼠中仍比亲本180P疫苗更具毒力。此外,在嵌合病毒180P/JEV - prM - E中引入单个E突变进一步减弱了病毒,这在小鼠模型中提供了针对强毒JEV株攻击的完全保护。这些结果表明,FX2010 - 180P可作为黄病毒疫苗开发的一个有前景的骨架。