Development of a live-attenuated chimeric vaccine against the emerging Usutu virus

被引:2
作者
Wang, Zheng-Jian [1 ]
Zhang, Rong-Rong [1 ]
Wu, Mei [1 ]
Zhao, Hui [1 ]
Li, Xiao-Feng [1 ]
Ye, Qing [1 ]
Qin, Cheng-Feng [1 ,2 ]
机构
[1] Beijing Inst Microbiol & Epidemiol, State Key Lab Pathogen & Biosecur, Beijing 100071, Peoples R China
[2] Chinese Acad Med Sci, Res Unit Discovery & Tracing Nat Focus Dis, Beijing 100071, Peoples R China
关键词
Usutu virus (USUV); Emerging flavivirus; Chimeric virus; Live -attenuated vaccine; Immune protection; WEST-NILE-VIRUS; JAPANESE ENCEPHALITIS; FLAVIVIRUS; INDUCTION; MICE; SENSITIVITY; INFECTION; SA14-14-2;
D O I
10.1016/j.vaccine.2024.01.077
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Usutu virus (USUV) is an emerging arthropod-borne flavivirus that has expanded into multiple European countries during the past several decades. USUV infection in human has been linked to severe neurological complications, and no vaccine is now available against USUV. In this work, we develop a live-attenuated chimeric USUV vaccine (termed ChinUSUV) based on the full-length infectious cDNA clone of the licensed Japanese encephalitis virus (JEV) vaccine strain SA14-14-2. In vitro studies demonstrate that ChinUSUV replicates efficiently and maintains its genetic stability. Remarkably, ChinUSUV exhibits a significant attenuation phenotype in multiple mouse models even compared with the licensed JEV vaccine. A single immunization with ChinUSUV elicits potent IgG and neutralizing antibody responses as well as T cell response. Passive transfer of sera from ChinUSUV-immunized mice confers significant protection against lethal homologous challenge in suckling mice. Taken together, our results suggest that ChinUSUV represents a potential USUV vaccine candidate that merits further development.
引用
收藏
页码:1363 / 1371
页数:9
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