建立和描述一个复制受限制的修饰的非洲猪瘟病毒
Tomoya Kitamura1, Kentaro Masujin1, Mitsutaka Ikezawa1
1National Institute of Animal Health (NIAH), National Agriculture and Food Research Organization (NARO), Kodaira, Tokyo, Japan.
Microbiology spectrum
|December 23, 2025
概括
开发一种更安全的非洲猪瘟病毒 (ASFV) 疫苗需要通过删除S273R基因来创建一个具有复制限制的ASFV菌株. 这种新型候选疫苗在猪中没有显示任何临床症状,并且提供了对ASFV的部分保护.
科学领域:
- 兽医病毒学 兽医病毒学
- 传染性疾病 传染性疾病
- 疫苗开发 疫苗开发
背景情况:
- 非洲猪瘟 (ASF) 是一种高度传染性和致命的疾病,影响猪和野猪,由非洲猪瘟病毒 (ASFV) 引起.
- 目前使用活体减弱ASFV的疫苗策略引发了生物安全问题,原因是潜在的毒性逆转和二次传播.
- 自2007年出现以来,ASFV (基因型II) 的流行病菌株已在全球传播.
研究的目的:
- 开发一种具有增强生物安全性的新型,复制受限制的ASFV疫苗候选物.
- 解决与活体减弱ASFV疫苗相关的问题,例如长期持久性和病毒性逆转.
主要方法:
- 通过删除对病毒成熟至关重要的S273R基因,创建了一个复制受限制的ASFV菌株 (AQSΔS273R).
- 用S273R基因补充的永生猪巨细胞被建立起来,以使病毒在体外传播.
- 猪被免疫了AQSΔS273R,随后被挑战了有毒的ASFV.
主要成果:
- 该AQSΔS273R菌株无法在天然宿主细胞中复制,但在补充的猪巨中复制.
- 用AQSΔS273R免疫接种的猪没有出现临床症状或病毒病.
- 用AQSΔS273R接种疫苗对病毒性ASFV挑战产生约30%的保护,临床症状减少.
结论:
- 通过删除S273R基因来开发复制受限ASFV是一种可行的方法,用于创建更安全的疫苗候选人.
- 与传统的活体减弱疫苗相比,这种新的ASFV疫苗策略提供了增强的生物安全性.
- AQSΔS273R菌株代表了非洲猪瘟的有希望和生物安全的疫苗候选人.
相关概念视频
Viral Recombination
Cells are sometimes infected by more than one virus at once. When two viruses disassemble to expose their genomes for replication in the same cell, similar regions of their genomes can pair together and exchange sequences in a process called recombination. Alternatively, viruses with segmented genomes can swap segments in a process called reassortment.
Subviral Agents
Subviral agents are infectious entities that resemble viruses but lack one or more viral components, such as a capsid or essential replication machinery. These agents include viroids, prions, and satellites, each possessing distinct structural and functional characteristics that influence their mode of infection and replication.Viroids are the simplest subviral agents, consisting of circular, single-stranded RNA molecules without a protein coat. They exclusively infect plants, relying entirely...
Inhibitors of Virion Maturation and Assembly
As part of their replication cycle, certain viruses synthesize long precursor proteins called polyproteins within infected host cells. In human immunodeficiency virus (HIV), two major polyproteins are produced: Gag and Gag-Pol. The Gag polyprotein supplies the structural components of the virus, while Gag-Pol includes essential viral enzymes such as reverse transcriptase, integrase, and protease. After synthesis, these polyproteins move to the host cell membrane, where they assemble into an...


