Huang Ruojia, Luo Rui, Lan Jing, Lu Zhanhao, Qiu Hua-Ji, Wang Tao, Sun Yuan
State Key Laboratory for Animal Disease Control and Prevention, National African Swine Fever Para-Reference Laboratory, National High Containment Facilities for Animal Diseases Control and Prevention, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Harbin 150069, China.
Viruses. 2025 Jun 19;17(6):865. doi: 10.3390/v17060865.
African swine fever virus (ASFV), the causative agent of African swine fever (ASF), poses a catastrophic threat to global swine industries through its capacity for immune subversion and rapid evolution. Multigene family genes (MGFs)-encoded proteins serve as molecular hubs governing viral evolution, immune evasion, cell tropism, and disease pathogenesis. This review synthesizes structural and functional evidence demonstrating that MGFs-encoded proteins suppress both interferon signaling and inflammasome activation, while their genomic plasticity in variable terminal regions drives strain diversification and adaptation. Translationally, targeted deletion of immunomodulatory MGFs enables the rational design of live attenuated vaccines that improve protective efficacy while minimizing residual virulence. Moreover, hypervariable MGFs provide strain-specific signatures for PCR-based diagnostics and phylogeographic tracking, directly addressing outbreak surveillance challenges. By unifying virology with translational innovation, this review establishes MGFs as priority targets for next-generation ASF countermeasures.
非洲猪瘟病毒(ASFV)是非洲猪瘟(ASF)的病原体,它具有免疫颠覆和快速进化的能力,对全球养猪业构成了灾难性威胁。多基因家族基因(MGFs)编码的蛋白质是控制病毒进化、免疫逃避、细胞嗜性和疾病发病机制的分子枢纽。本综述综合了结构和功能证据,证明MGFs编码的蛋白质既抑制干扰素信号传导,也抑制炎性小体激活,而它们在可变末端区域的基因组可塑性驱动毒株多样化和适应性。在转化应用方面,对免疫调节性MGFs进行靶向缺失能够合理设计减毒活疫苗,提高保护效力,同时将残余毒力降至最低。此外,高变MGFs为基于PCR的诊断和系统发育地理追踪提供毒株特异性特征,直接应对疫情监测挑战。通过将病毒学与转化创新相结合,本综述将MGFs确立为下一代ASF应对措施的优先靶点。