A Pool of Bacterium-like Particles Displaying African Swine Fever Virus Antigens Induces Both Humoral and Cellular Immune Responses in Pigs
文献类型： 外文期刊
作者： Huang, Jingshan 1 ; Wu, Hongxia 1 ; Gao, Tianqi 1 ; Zhai, Huanjie 1 ; Moon, Assad 1 ; Song, Xin 1 ; Li, Shuwen 1 ; Lu, Zhanhao 1 ; Lan, Jing 1 ; Zhong, Dailang 1 ; Zhang, Xinyu 1 ; Qiu, Hua-Ji 1 ; Li, Yongfeng 1 ; Sun, Yuan 1 ;
作者机构： 1.Chinese Acad Agr Sci, Harbin Vet Res Inst, State Key Lab Anim Dis Control & Prevent, Natl African Swine Fever Para Reference Lab, Harbin 150069, Peoples R China
2.Jilin Agr Univ, Coll Anim Sci & Technol, Jilin Prov Engn Res Ctr Anim Probiot, Key Lab Anim Prod & Prod Qual Safety,Minist Educ, Changchun 130118, Peoples R China
关键词： bacterium-like particles; African swine fever; Gram-positive enhancer matrix; immunological evaluation
期刊名称：VACCINES （ 影响因子：3.4； 五年影响因子：3.7 ）
ISSN：
年卷期： 2025 年 13 卷 1 期
页码：
收录情况： SCI
摘要： Background/Objectives: African swine fever (ASF), caused by African swine fever virus (ASFV), poses a significant threat to the global swine industry. This underscores the urgent need for safe and effective ASF vaccines. Methods: Here, we constructed five bacterium-like particles (BLPs) that each display one of the five ASFV antigens (F317L, H171R, D117L, B602L, and p54) based on the Gram-positive enhancer matrix-protein anchor (GEM-PA) system. GEM is a bacterial particle that contains only peptidoglycan, while PA is composed of three lysin motifs (Lysm) derived from the C-terminus of the AcmA protein, capable of non-covalently binding to GEM. By fusing the ASFV antigens with PA, the ASFV antigens can be firmly attached to the surface of GEM. Subsequently, the piglets were immunized via intramuscular injection with a mixture of BLPs-F317L, BLPs-H171R, BLPs-D117L, BLPs-B602L, and BLPs-p54. Results: The results showed that the piglets developed detectable serum IgG antibodies 2 weeks after the first immunization, and these high antibody levels were maintained 4 weeks after the booster immunization. Moreover, these piglets produced more IFN-gamma-producing lymphocytes than the control piglets. Conclusions: The data indicate that the generated BLPs mixture can stimulate both humoral and cellular immune responses in piglets, these five ASFV proteins are promising antigens, and the BLPs generated represent candidate ASF vaccines.
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