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纳米颗粒MntC-rePO@LS双联疫苗的构建及其对铜绿假单胞菌与金黄色葡萄球菌感染的免疫保护效果研究

赵辉 余瑛 李宇航 张月月 胡仁建 夏欢 朱自凡 刘兴龙 张怡 顾江

陆军军医大学学报2026,Vol.48Issue(8):1003-1013,11.
陆军军医大学学报2026,Vol.48Issue(8):1003-1013,11.DOI:10.16016/j.2097-0927.202512104

纳米颗粒MntC-rePO@LS双联疫苗的构建及其对铜绿假单胞菌与金黄色葡萄球菌感染的免疫保护效果研究

Bivalent nanovaccine MntC-rePO@LS conffers efective protections against Pseudomonas aeruginosa and Staphylococcus aureus

赵辉 1余瑛 2李宇航 3张月月 4胡仁建 2夏欢 4朱自凡 3刘兴龙 5张怡 3顾江3

作者信息

  • 1. 重庆理工大学药学与生物工程学院,重庆||陆军军医大学(第三军医大学)药学与检验医学系微生物与生化药学教研室,国家免疫生物制品工程技术研究中心,重庆
  • 2. 重庆理工大学药学与生物工程学院,重庆
  • 3. 陆军军医大学(第三军医大学)药学与检验医学系微生物与生化药学教研室,国家免疫生物制品工程技术研究中心,重庆
  • 4. 重庆原伦生物科技有限公司,重庆
  • 5. 陆军军医大学(第三军医大学)药学与检验医学系微生物与生化药学教研室,国家免疫生物制品工程技术研究中心,重庆||陆军军医大学(第三军医大学)第二附属医院呼吸与危重症医学科,重庆
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摘要

Abstract

Objective The escalating threat of antimicrobial resistance poses significant clinical challenges,particularly in cases of co-infections involving Staphylococcus aureus(SA)and Pseudomonas aeruginosa(PA),which synergistically increase disease severity and complicate therapeutic interventions.A bivalent nanovaccine,MntC-rePO@LS,was constructed by co-displaying the SA antigen Manganese transporter C(MntC)and the PA recombinant PcrV-OprI fusion antigen(rePO)based on self-assembling lumazine synthase(LS)nanoparticles.We hypothesized that this vaccine would provide superior immunoprotection against both single and co-infections with SA and PA compared to monomeric or physically mixed formulations.Methods The MntC-rePO@LS bivalent nanoparticles were prepared using genetic engineering and the SpyTag/SpyCatcher system.Female BALB/c mice(6 to 8 weeks old,weighing 18 to 20 g)were randomly divided into 6 groups:PBS,LS(8.57 μg LS),rePO(9.43 μg rePO),MntC(10 μg MntC),physical mixture(8.57 μg LS,10 μg MntC,and 9.43 μg rePO),and MntC-rePO@LS(10.86 μg rePO-ST and 18.57 μg MntC@LS)groups,with 5 animals in each group.The mice from the above groups were immunized intramuscularly with corresponding agents dissolved in PBS buffer on days 0,7,and 14.The vaccine was characterized by SDS-PAGE,size-exclusion chromatography,dynamic light scattering,and transmission electron microscopy(TEM).In vitro and in vivo safety of the vaccine was assessed through hemolysis assay,cytotoxicity test,body weight monitoring,histopathological examination,and hematological and serum biochemical analyses.The serum samples were collected on day 7 after the final immunization,and the titers and subtypes of anti-MntC and anti-rePO IgG were evaluated by indirect ELISA to evaluate the immunogenicity of the vaccine.Protective efficacy was assessed in mouse pneumonia models of single PA,single SA,and PA/SA co-infections by monitoring body weight and infection scores post-challenge,and by quantifying lung bacterial loads and observing histopathological changes at 24 h post-challenge.Results We successfully constructed homogeneous MntC-rePO@LS nanoparticles with a hydrodynamic diameter of approximately 65.69 nm.The vaccine exhibited no significant hemolysis or cytotoxicity at concentrations ranging from 10 to 200 μg/mL.The immunized mice demonstrated normal body weight gain,with no pathological damage observed in major organs or at the injection site,and all hematological and biochemical parameters remained within normal ranges.Immunogenicity studies revealed that the MntC-rePO@LS group induced significantly higher anti-MntC and anti-rePO specific IgG titers at all 3 time points tested(day 0,7,and 14)compared to monomer and physical mixture groups(P<0.05),with a predominant IgG2b subtype response.In the models of single PA,single SA,and co-infections,the MntC-rePO@LS group exhibited faster body weight recovery,lower infection scores,significantly reduced bacterial loads in the lungs(P<0.05),and markedly attenuated lung histopathological damage compared to all control groups.Conclusion The successfully constructed MntC-rePO@LS bivalent nanovaccine demonstrates favorable safety and immunogenicity,providing significant immune protection against single and co-infections with SA and PA.These findings validate its potential as a candidate vaccine to address antimicrobial resistance and polymicrobial infections.

关键词

双联纳米疫苗/铜绿假单胞菌/金黄色葡萄球菌/免疫保护

Key words

bivalent nanovaccine/Pseudomonas aeruginosa/Staphylococcus aureus/immunoprotection

分类

医药卫生

引用本文复制引用

赵辉,余瑛,李宇航,张月月,胡仁建,夏欢,朱自凡,刘兴龙,张怡,顾江..纳米颗粒MntC-rePO@LS双联疫苗的构建及其对铜绿假单胞菌与金黄色葡萄球菌感染的免疫保护效果研究[J].陆军军医大学学报,2026,48(8):1003-1013,11.

基金项目

国家重点研发计划(2024YFC2310801) (2024YFC2310801)

国家自然科学基金青年科学基金项目(82502215) Supported by the National Key Research and Development Program(2024YFC2310801)and the National Natural Science Foundation for Young Scholars of China(82502215). (82502215)

陆军军医大学学报

2097-0927

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