畜牧兽医学报 ›› 2025, Vol. 56 ›› Issue (9): 4626-4637.doi: 10.11843/j.issn.0366-6964.2025.09.040

• 预防兽医 • 上一篇    下一篇

产气荚膜梭菌α毒素-铁蛋白纳米颗粒抗原制备及其对小鼠的免疫原性评价

赵慧玉1,2, 雷伊诺2,3, 幸倩如2, 张珊2, 张广智2, 蒋卉2, 沈青春2, 丁家波2, 姜世金1*, 范学政2*   

  1. 1. 山东农业大学, 泰安 271000;
    2. 中国农业科学院北京畜牧兽医研究所, 北京 100193;
    3. 广西大学, 南宁 530004
  • 收稿日期:2024-12-18 发布日期:2025-09-30
  • 通讯作者: 范学政,主要从事人畜共患病、重大传染病兽用新型疫苗、新型诊断试剂研发工作,E-mail:fanxuezheng@caas.cn;姜世金,主要从事兽医分子病原学及免疫学等方面的研究,E-mail:jshijin@163.com
  • 作者简介:赵慧玉(1999-),女,山东莒南人,硕士,主要从事动物微生物学和免疫学研究,E-mail:1765137226@qq.com;雷伊诺(2000-),女,山西长治人,硕士,主要从事动物微生物学和免疫学研究,E-mail:1229042392@qq.com。
  • 基金资助:
    宁夏重点研发项目(2024BBF02014);中国农科院创新工程重点项目(CAAS-CSLPDCP-202403)

Preparation of Clostridium perfringens α Toxin-ferritin Nanoparticle Antigens and Evaluation of Its Immunogenicity in Mice

ZHAO Huiyu1,2, LEI Yinuo2,3, XING Qianru2, ZHANG Shan2, ZHANG Guangzhi2, JIANG Hui2, SHEN Qingchun2, DING Jiabo2, JIANG Shijin1*, FAN Xuezheng2*   

  1. 1. Shandong Agricultural University, Tai'an 271000, China;
    2. Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing 100193, China;
    3. Guangxi University, Nanning 530004, China
  • Received:2024-12-18 Published:2025-09-30

摘要: 本研究旨在制备产气荚膜梭菌α毒素-铁蛋白纳米颗粒抗原并评价其对小鼠的免疫原性。将带有D56G、H68G点突变和Spytag序列的α毒素全长基因和带有SpyCatcher序列的铁蛋白(Ferritin)基因片段分别克隆至原核表达载体pET 28a,后进行表达并对表达产物进行鉴定和纯化。对纯化后的αm2ST进行细胞毒性、卵磷脂酶活性以及溶血活性分析。将纯化的αm2ST和FeSC在体外对接,随后,将α毒素-铁蛋白(αm2-Fe)对接产物和αm2ST分别与佐剂混合后免疫小鼠。免疫后每周采集小鼠血清,检测IgG、IgG亚型抗体水平和中和效价,并在二免后28 d取脾细胞分析T细胞亚群和IFN-γ分泌水平。结果显示,在28 ℃条件下,αm2ST和FeSC均以可溶性表达为主。αm2ST未被检测出细胞毒性、卵磷脂酶活性和溶血活性,这说明αm2ST已无毒性。将αm2ST和FeSC体外对接后,经SDS-PAGE、TEM和DLS分析,证实αm2-Fe形成直径32.7~50.7 nm的纳米颗粒,主峰为37.8 nm。小鼠免疫后,αm2-Fe组能产生较高水平的IgG2a抗体(P<0.001);小鼠二免后21 d,αm2-Fe组血清中和效价为64倍,显著高于αm2ST组的32倍(P<0.05);二免后28 d,αm2-Fe组脾细胞刺激后上清中的IFN-γ也高于αm2ST组(P<0.05),流式细胞术分析显示αm2-Fe组产生了较高比例的效应性CD8+ T细胞(P<0.000 1)。小鼠试验证实αm2-Fe纳米颗粒抗原能有效刺激小鼠产生体液免疫和细胞免疫。

关键词: 产气荚膜梭菌, α毒素, 铁蛋白, 纳米颗粒, 免疫原性

Abstract: This study aimed to prepare Clostridium perfringens α-ferritin nanoparticle antigens and evaluate its immunogenicity in mice. The full-length α gene containing D56G and H68G point mutations and the Spytag sequence, as well as the gene fragment ferritin containing the ferritin gene and SpyCatcher sequence were cloned into the prokaryotic expression vector pET 28a vector respectively. Recombinant proteins were expressed followed by identification and purification. The cytotoxicity, lecithinase activity and haemolytic activity of purified αm2ST were analysed. The purified αm2ST and FeSC were docked in vitro. The docking product of α-ferritin (αm2-Fe) and αm2ST were mixed with adjuvant, respectively, and used for mice immunization. Mice serum was collected every week post immunization to measure IgG, IgG subtype antibody levels and the serum neutralization titers; on day 28 post the second immunization, splenocytes were isolated to analyze T-cell subsets and IFN-γ secretion levels. The results showed that at 28 ℃, αm2ST and FeSC were predominantly expressed in a soluble manner. The αm2ST was free of cytotoxicity, lecithinase activity, or hemolytic activity after detection, indicating that the αm2ST is non-toxic. After in vitro docking of αm2ST and FeSC, it was confirmed that the αm2-Fe formed nanoparticles with a diameter of 32.7-50.7 nm, with a main peak at 37.8 nm, after analyses with SDS-PAGE, TEM, and DLS. Following immunization in mice, the αm2-Fe group exhibited high levels of IgG2a antibodies (P<0.001). On day 21 after the second immunization, the serum neutralization titer in the αm2-Fe group was 64-fold, significantly surpassing the 32-fold titer in the αm2ST group (P<0.05). By day 28 after the second immunization, the IFN-γ levels in the supernatant of stimulated splenocytes were also higher in the αm2-Fe group compared to the αm2ST group (P<0.05). Flow cytometry analysis revealed that the αm2-Fe group produced a higher proportion of effector CD8+ T cells (P<0.000 1). Mice experiments confirmed that the αm2-Fe nanoparticle antigens effectively induce both humoral and cellular immunity in mice.

Key words: Clostridium perfringens, alpha toxin, ferritin, nanoparticles, immunogenicity

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